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DTSTART:19450814T190000
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BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:Flavins are one of life's earliest catalysts and continue to p
 lay critical roles in the energy metabolism required to support life's co
 mplexity. The flavin's virtuosity and versatility enable it to mediate di
 verse reactions\, making it one of life's go-to cofactors. However in any
  one role\, the host protein must ensure that the flavin is optimized for
  a single function and others are suppressed. In bifurcating electron tra
 nsfer flavoproteins\, two chemically identical flavins play contrasting r
 oles.  We are combining biochemical experiments\, spectroscopy and comput
 ation to learn how individual hydrogen bonds\, local electrostatics\, del
 ocalized hydrogen bond networks and domain-scale conformational changes d
 etermine and respond to flavin activity.
DURATION:PT1H
DTSTAMP:20240210T030653Z
DTSTART;TZID=America/New_York:20240226T120000
LAST-MODIFIED:20240210T030653Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Quantum Computational Insights Into the Chemical Versatility and S
 pectral Signatures of Flavins
UID:CAL-8a0292fd-8d13410f-018d-90fa3d85-00007c8fdemobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_Schoolo
 fMedicine_BiostatisticsandBioinformatics,/principals/users/agrp_Centerfor
 GenomicandComputationalBiology,/principals/users/agrp_AGPM_Collaboratory,
 /principals/users/agrp_SchoolofMedicine,":Biostatistics and Bioinformatic
 s\,Duke Center for Genomic and Computational Biology (GCB)\,Precision Gen
 omics Collaboratory\,School of Medicine (SOM)
X-BEDEWORK-SPEAKER:Anne-Frances Miller
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Anne-Frances Miller\, PhD\, Distinguished Profes
 sor\, Arts and Sciences at University of Kentucky
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Anne-Frances Miller canva photo_2024021003
 0534AM.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Anne-Frances Miller canva photo_2024
 0210030534AM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:Early identification of autism\, ADHD\, and other neurodevelop
 mental conditions is important to ensure children receive appropriate dev
 elopmental support and thereby optimize long term outcomes. Early correla
 tes of these conditions are documented in the electronic health record (E
 HR) during routine care\, and our previous work has shown that EHR data c
 an be leveraged to predict autism and ADHD likelihood with clinically mea
 ningful accuracy prior to age 1. Much like other EHR-based prediction tas
 ks\, this task is challenging due to the high-dimensional\, multi-modal\,
  irregularly observed nature of the relevant predictors. Additionally\, o
 ther challenges are amplified due to the breadth of the target population
  (all children) and length of time between prediction and outcome (severa
 l years). Specifically\, there is substantial variability in the quantity
  and quality of data available for prediction\, average follow-up length 
 is much lower than average time to diagnosis\, and time to diagnosis is a
 ffected by systemic biases associated with the diagnosis process. This ta
 lk will explore methods we have developed in response to these challenges
 \, with emphasis on a neural mixture cure model designed to disentangle f
 actors affecting the age at diagnosis from factors affecting lifetime dia
 gnosis probability.
DURATION:PT1H
DTSTAMP:20240226T141451Z
DTSTART;TZID=America/New_York:20240304T120000
LAST-MODIFIED:20240226T141451Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Methods for Long-Horizon Event Prediction from Electronic Health R
 ecord Data
UID:CAL-8a0292fd-8d13410f-018d-e5c415ba-00001d5ddemobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_Schoolo
 fMedicine_BiostatisticsandBioinformatics,/principals/users/agrp_Centerfor
 GenomicandComputationalBiology,/principals/users/agrp_AGPM_Collaboratory,
 /principals/users/agrp_SchoolofMedicine,":Biostatistics and Bioinformatic
 s\,Duke Center for Genomic and Computational Biology (GCB)\,Precision Gen
 omics Collaboratory\,School of Medicine (SOM)
X-BEDEWORK-SPEAKER:Matt Engelhard
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Matt Engelhard\, Phd\, Assistant Professor\, Dep
 artment of Biostatistics and Bioinformatics\, Duke University
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Matt Engelhard canva photo_20240226021409P
 M.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Matt Engelhard canva photo_202402260
 21409PM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:Genetic prediction of molecular traits help bridge the gap bet
 ween genotype and phenotype especially by integrating them with GWAS stud
 ies. These prediction models are trained using reference datasets where h
 undreds of individuals with genotype and omics data are collected. Emergi
 ng methods in deep learning using state of the art architectures such as 
 transformers promise to improve prediction approaches and reduced the nec
 essary sample sizes. I will discuss current opportunities and challenges 
 of deep learning approaches to inform the biology of complex diseases.
DURATION:PT1H
DTSTAMP:20240302T223937Z
DTSTART;TZID=America/New_York:20240318T120000
LAST-MODIFIED:20240302T223937Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Incorporating Deep Learning Methods to Complex Trait Genetics
UID:CAL-8a0292fd-8d13410f-018e-015064d8-00004ba1demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_Schoolo
 fMedicine_BiostatisticsandBioinformatics,/principals/users/agrp_Centerfor
 GenomicandComputationalBiology,/principals/users/agrp_AGPM_Collaboratory,
 /principals/users/agrp_SchoolofMedicine,":Biostatistics and Bioinformatic
 s\,Duke Center for Genomic and Computational Biology (GCB)\,Precision Gen
 omics Collaboratory\,School of Medicine (SOM)
X-BEDEWORK-SPEAKER:Hae Kyung Im
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Hae Kyung Im\, PhD\, Associate Professor\, Depar
 tment of Human Genetics at the University of Chicago
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Hae Kyung Im canva photo_20240302103709PM.
 png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Hae Kyung Im canva photo_20240302103
 709PM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:The rapid development of single-cell and spatial omics technol
 ogies has propelled fast advances in computational algorithms. However\, 
 the statistical rigor in data analysis has been often overlooked. Motivat
 ed by the mandatory use of negative controls in experiments\, I propose t
 o enhance the reliability of single-cell and spatial omics data analysis 
 by using synthetic negative controls generated based on real data under s
 pecific null hypotheses. I will demonstrate this strategy using two stati
 stical methods my group developed. First\, using permutation to generate 
 a synthetic negative control in which cell-cell relationships are disrupt
 ed\, we developed a statistical method\, scDEED (https://doi.org/10.1101/
 2023.04.21.537839)\, to detect dubious two-dimensional cell embeddings\, 
 crucial for single-cell data visualization\, and to optimize the hyperpar
 ameters of embedding methods such as t-SNE and UMAP. Second\, using our s
 imulator scDesign3 (https://www.nature.com/articles/s41587-023-01772-1) t
 o generate synthetic null controls\, we developed a statistical method\, 
 ClusterDE (https://doi.org/10.1101/2023.07.21.550107)\, to identify poten
 tial cell-type markers (or spatial domain markers) from differential expr
 ession (DE) analysis applied to potential cell types (or spatial domains)
  identified through clustering analysis. Overall\, leveraging synthetic n
 egative controls is an effective strategy to increase the statistical rig
 or of complex data analysis and thus improve the reliability of analysis 
 results.
DURATION:PT1H
DTSTAMP:20240304T022444Z
DTSTART;TZID=America/New_York:20240325T120000
LAST-MODIFIED:20240304T022444Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Enhancing Statistical Rigor in Single-Cell and Spatial Omics Data 
 Analysis Using Synthetic Negative Controls
UID:CAL-8a0292fd-8d13410f-018e-05d8c1cc-000060b8demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_Schoolo
 fMedicine_BiostatisticsandBioinformatics,/principals/users/agrp_Centerfor
 GenomicandComputationalBiology,/principals/users/agrp_AGPM_Collaboratory,
 /principals/users/agrp_SchoolofMedicine,":Biostatistics and Bioinformatic
 s\,Duke Center for Genomic and Computational Biology (GCB)\,Precision Gen
 omics Collaboratory\,School of Medicine (SOM)
X-BEDEWORK-SPEAKER:Jessica Li
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:-0.3333333333333144
X-BEDEWORK-IMAGE-X2:530
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:530
X-BEDEWORK-IMAGE-CROP-HEIGHT:353.3333333333333
X-BEDEWORK-IMAGE-ALT-TEXT:Jessica Li\, PhD\, Professor in the Department o
 f Statistics University of California\, Los Angeles
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Jessica Li canva photo_20240304022444AM.pn
 g
X-BEDEWORK-THUMB-IMAGE:/public/Images/Jessica Li canva photo_2024030402244
 4AM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:Efforts to repurpose CRISPR-Cas systems have produced a suite 
 of genome editing tools\, including programmable nucleases\, base editors
 \, and prime editors. These tools have greatly enabled the study of genom
 es and gene function\, and their advancement to therapeutic development h
 as demonstrated promise for addressing a host of unmet medical needs. Our
  understanding of how endogenous cellular processes influence the activit
 y of these tools\, however\, lags far behind their application and\, due 
 to the rapid pace of technology development\, behind efforts to build new
  approaches. Our work focuses on identifying cellular determinants of gen
 ome editing tools to better understand how they work. Our results provide
  key insights into how those tools interact with the cellular environment
  and suggest general strategies for improvement.
DURATION:PT1H
DTSTAMP:20240318T202436Z
DTSTART;TZID=America/New_York:20240401T120000
LAST-MODIFIED:20240318T202436Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Mapping the Cellular Determinants of Genome  Editing in Human Cell
 s
UID:CAL-8a0292fd-8d13410f-018e-521ac7ab-00004a0bdemobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_Schoolo
 fMedicine_BiostatisticsandBioinformatics,/principals/users/agrp_Pratt_CAG
 T,/principals/users/agrp_CenterforGenomicandComputationalBiology,/princip
 als/users/agrp_AGPM_Collaboratory,/principals/users/agrp_SchoolofMedicine
 ,":Biostatistics and Bioinformatics\,Center for Advanced Genomic Technolo
 gies\,Duke Center for Genomic and Computational Biology (GCB)\,Precision 
 Genomics Collaboratory\,School of Medicine (SOM)
X-BEDEWORK-SPEAKER:Britt Adamson
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Britt Adamson\, PhD\, Assistant Professor\, Mole
 cular Biology\, Lewis Sigler Institute of Integrative Genomics\, Princeto
 n University
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Britt Adamson canva photo_20240318030750PM
 .png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Britt Adamson canva photo_2024031803
 0750PM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:Single-cell paired multi-omic data\, such as jointly sequenced
  RNA and ATAC via 10x Multiome\, has been widely adopted to study the reg
 ulatory mechanisms in different biological systems. However\, there are s
 till open questions on how to broadly measure the coordination between th
 ese two modalities within individual cells and account for the changing c
 oordination over time. In this talk\, we discuss two different lines of w
 ork with similar themes that model the RNA-ATAC coordination holistically
 . In the first half of the talk regarding cortical development\, we prese
 nt the Tilted-CCA\, a new statistical decomposition that uncovers the com
 mon and modality-unique geometric relations among cells. This decompositi
 on gives us a new perspective for studying development since a gradual in
 crease and decrease of RNA-ATAC coordination can mathematically quantify 
 the poised chromatin state. In the second half of the talk regarding canc
 er resistance\, we present a cell-wise lineage imputation score. This sta
 tistical regression method uses static lineage barcoding data that our co
 llaborators have developed to work with the 10x Multiome. Our method offe
 rs new insight into cancer resistance mechanisms\, as our statistical met
 hod can assess how many progenies each cancer cell is likely to produce a
 t a future time. This method allows us to quantify how a cancer subclone'
 s lineage size\, its RNA+ATAC profile\, and its plasticity contribute tow
 ards said subclone's resistant behavior.
DURATION:PT1H
DTSTAMP:20240325T182308Z
DTSTART;TZID=America/New_York:20240408T120000
LAST-MODIFIED:20240325T182308Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Single-Cell Paired RNA & ATAC: Surveying broad multi-modal coordin
 ation in development and cancer resistance
UID:CAL-8a0292fd-8d13410f-018e-76d950f6-00003842demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_Schoolo
 fMedicine_BiostatisticsandBioinformatics,/principals/users/agrp_Centerfor
 GenomicandComputationalBiology,/principals/users/agrp_AGPM_Collaboratory,
 /principals/users/agrp_SchoolofMedicine,":Biostatistics and Bioinformatic
 s\,Duke Center for Genomic and Computational Biology (GCB)\,Precision Gen
 omics Collaboratory\,School of Medicine (SOM)
X-BEDEWORK-SPEAKER:Kevin Lin
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Kevin Lin\, PhD\, Assistant Professor in the Sch
 ool of Public Health\, Biostatistics at University of Washington
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Kevin Lin canva photo_20240325062216PM.png
 
X-BEDEWORK-THUMB-IMAGE:/public/Images/Kevin Lin canva photo_20240325062216
 PM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:The Lareau lab works to decipher the layers of information enc
 oded in the genome that specify cellular form and function. We use machin
 e learning and high throughput experiments to model how sequence determin
 es the output of the genome as it is transcribed into RNA then translated
  into protein.
DURATION:PT1H
DTSTAMP:20240329T134421Z
DTSTART;TZID=America/New_York:20240415T120000
LAST-MODIFIED:20240329T134421Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Engineering Poison Exons to Treat Huntington’s Disease
UID:CAL-8a0292fd-8d13410f-018e-8a741099-00001c4cdemobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_Schoolo
 fMedicine_BiostatisticsandBioinformatics,/principals/users/agrp_AGPM_Coll
 aboratory,/principals/users/agrp_SchoolofMedicine,":Biostatistics and Bio
 informatics\,Precision Genomics Collaboratory\,School of Medicine (SOM)
X-BEDEWORK-SPEAKER:Liana Lareau
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Liana Lareau\, PhD\, Assistant Professor in the 
 Department of Bioengineering at the University of California\, Berkeley
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Liana Lareau canva photo_20240329014405PM.
 png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Liana Lareau canva photo_20240329014
 405PM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=00f1fcdb-0f068baf-010f-068baf83-00000004:None
CREATED:20230828T005529Z
DESCRIPTION:The Department of Chemistry is excited to host Lisa Olshansky 
 (University of Illinois Urbana-Champaign)\nTo learn more about the Olshan
 sky lab's work\, please visit their research page: https://www.olshanskyl
 ab.chemistry.illinois.edu/\n\nEmergent Properties from Dynamicity: \nInve
 stigating Conformational Control in Biomimetic Inorganic Systems\nFrom th
 e reduction of dinitrogen to the oxidation of water\, the chemical transf
 ormations catalyzed by metalloenzymes underpin global geo- and biochemica
 l cycles. These reactions represent some of the most kinetically and ther
 modynamically challenging processes known. Interestingly\, rate-limiting 
 conformational changes precede catalysis in many metalloenzymes. The perv
 asiveness of this mechanistic pattern suggests that conformational gating
  may play an important role in mediating challenging chemical transformat
 ions in an energy-efficient manner. However\, these enzymes are extremely
  complex\, rendering direct examination of their conformational gating st
 eps a tremendous challenge. Instead\, we have taken the unique approach o
 f preparing model systems in which macroscopic changes in the molecular s
 tructure of a ligand or protein host give rise to subatomic changes in th
 e electronic structure of a bound metal ion. These systems include both c
 onformationally dynamic coordination complexes and conformationally switc
 hable artificial metalloproteins. In both cases\, exciting new properties
  have emerged from the structural dynamicity at play. Ultimately\, our wo
 rk with these systems aims to define and quantify the kinetic and thermod
 ynamic consequences of conformational gating mechanisms. Additionally\, t
 he systems under development are molecular switches and can also be explo
 ited in applications ranging from solar energy conversion\, to biomedical
  imaging\, to green methods in chemical catalysis.\n\nHosted by Kathy Fra
 nz
DURATION:PT1H
DTSTAMP:20240415T150746Z
DTSTART;TZID=America/New_York:20240417T150000
LAST-MODIFIED:20240415T150746Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Chemistry Seminar Presented by Prof. Lisa Olshansky: Emergent Prop
 erties from Dynamicity:  Investigating Conformational Control in Biomimet
 ic Inorganic Systems
UID:CAL-8a02906b-8a0a73d8-018a-39a37c31-000073a3demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-STUDENT-CONTACT;X-BEDEWORK-PARAM-EMAIL=chem-office@duke.edu:Che
 m Admin Office
X-BEDEWORK-SPEAKER:Lisa Olshansky\, University of Illinois Urbana-Champaig
 n
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:92
X-BEDEWORK-IMAGE-X2:1936
X-BEDEWORK-IMAGE-Y2:1382.6666666666667
X-BEDEWORK-IMAGE-CROP-WIDTH:1936
X-BEDEWORK-IMAGE-CROP-HEIGHT:1290.6666666666667
X-BEDEWORK-IMAGE-ALT-TEXT:Lisa Olshansky
X-BEDEWORK-SUBMITTEDBY:lao26 for Chemistry (agrp_ArtsandSciences_Chemistry
 )
X-BEDEWORK-IMAGE:/public/Images/Headshot_Olshansky_20240321022942PM.jpeg
X-BEDEWORK-THUMB-IMAGE:/public/Images/Headshot_Olshansky_20240321022942PM-
 thumb.png
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_Institu
 tes_MaterialsScienceandEngineering,/principals/users/agrp_PrattSchool_MEM
 S,":Duke Materials Initiative\,Mechanical Engineering and Materials Scien
 ce (MEMS)
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=00f1fcdb-0f068baf-010f-068baf83-00000004:None
CREATED:20240418T182025Z
DESCRIPTION:NC SER Symposium\n\nCharlie Cox will be hosting Regis Komperda
  (San Diego State University) for a seminar.\n\nMeasurement in chemistry 
 education: Examining the past and supporting the future \n \nAs with any 
 field of scientific research\, the ability to draw meaningful conclusions
  in chemistry education research (CER) is dependent on the use of appropr
 iate research methods\, including the selection of measurement instrument
 s (e.g.\, tests\, surveys\, concept inventories\, etc.) that will generat
 e high quality data about students and classrooms. This talk will discuss
  how CER has approached the concept of measurement quality (i.e.\, validi
 ty and reliability) and why the adoption of data quality standards is imp
 ortant for the development\, evaluation\, and dissemination of instrument
 s.\n\nCurrent research on measurement quality in CER will be presented to
  show the practical application of these standards for measuring student 
 attitudes and motivation in introductory chemistry courses. An NSF-suppor
 ted resource for finding chemistry education instruments and their associ
 ated data quality evidence\, the CHemistry Instrument Review and Assessme
 nt Library (CHIRAL\; chiral.chemedx.org)\, will be highlighted to support
  educators and researchers in finding instruments suitable for both class
 room and research contexts.\n\nThe Chemistry Instrument Review and Assess
 ment Library (CHIRAL) contains a catalog of over 500 assessment instrumen
 ts that is searchable by domain\, topic\, or format. Each listing in CHIR
 AL includes metadata (intended population\, language\, number of items\, 
 etc.) and reported evidence for validity and reliability. Select instrume
 nts include a panel review report providing a synthesis of the reported v
 alidity and reliability evidence. CHIRAL also contains a glossary of comm
 on terms used in psychometric evaluations to help understand the informat
 ion in CHIRAL. \n\nTo learn more about the Komperda Goroup's work\, pleas
 e visit their page at https://komperda-cer.sdsu.edu/
DURATION:PT1H
DTSTAMP:20240418T182025Z
DTSTART;TZID=America/New_York:20240607T140000
LAST-MODIFIED:20240418T182025Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:NC CER Symposium Seminar: Regis Komperda presents: Measurement in 
 chemistry education: Examining the past and supporting the future
UID:CAL-8a0292fd-8d13410f-018e-f2703e16-00000d33demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-SPEAKER:Regis Komperda- San Diego State University
X-BEDEWORK-STUDENT-CONTACT;X-BEDEWORK-PARAM-EMAIL=charlie.cox@duke.edu:Cha
 rlie Cox
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:417
X-BEDEWORK-IMAGE-X2:1913
X-BEDEWORK-IMAGE-Y2:1692.3333333333333
X-BEDEWORK-IMAGE-CROP-WIDTH:1913
X-BEDEWORK-IMAGE-CROP-HEIGHT:1275.3333333333333
X-BEDEWORK-IMAGE-ALT-TEXT:Komperda
X-BEDEWORK-SUBMITTEDBY:lao26 for Chemistry (agrp_ArtsandSciences_Chemistry
 )
X-BEDEWORK-IMAGE:/public/Images/Komperda-Headshot-scaled_20240418062025PM.
 jpg
X-BEDEWORK-THUMB-IMAGE:/public/Images/Komperda-Headshot-scaled_20240418062
 025PM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Conference/Symposium
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=00f1fcdb-0f068baf-010f-068baf83-00000004:None
CREATED:20220811T191533Z
DESCRIPTION:Taylor Outlaw\, Ph.D. Candidate\n\nKatherine Franz Ph.D.\, Adv
 isor\n\nAbstract: Metals play a vital role in living organisms by regulat
 ing many essential life processes. Metal homeostasis is essential for a h
 ealthy cell\, as metal overload and metal starvation can largely affect h
 ow biomolecules interact with one another. For this reason\, cells from a
 ll kingdoms of life have evolved mechanisms to control metal content incl
 uding metal importers and exporters\, metal storage proteins\, metallocha
 perones\, and metal-induced transcription factors. \nThis dissertation wi
 ll focus on the role of zinc and copper in specific biological systems. \
 nGlyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a highly conserved e
 nzyme\, most famous for its role in glycolysis. Previous work by the Fran
 z and Fitzgerald labs showed that copper-induced structural stability of 
 GAPDH from E. coli (ecGAPDH) alongside Cu2+-induced ecGAPDH inhibition in
  lysates. Building upon these findings\, my dissertation work characteriz
 ed the effects of copper on recombinant ecGAPDH through activity assays\,
  circular dichroism\, ICP-MS\, and copper-binding experiments. Both Cu2+ 
 and Cu+ can inhibit the activity of ecGAPDH\, though inhibition occurs vi
 a distinct mechanisms. In the presence of excess metal\, ecGAPDH is capab
 le of binding multiple equivalents of copper\, without changes to global 
 secondary structure. This leads us to question the role that ecGAPDH\, an
 d other homologs\, could play in intracellular copper trafficking. Next\,
  I present progress towards the antifungal mechanism of histatin-5\, a sa
 livary natural product with metal-dependent activity. The relationship be
 tween histatin-5\, copper\, zinc\, and Candida albicans has proven to be 
 complex and is susceptible to changes in temperature and extracellular en
 vironment. This nuanced relationship is likely a part of the more complex
  oral microbiome\, which can use metals and metal chelating proteins as a
 n innate immune response. Finally\, I present my chemical education resea
 rch project\, sponsored by the Bonk Fellowship\, that analyzed second-sem
 ester organic chemistry students' problem-solving strategies\, specifical
 ly focusing on the resources activated while ranking the acidity of vario
 us organic molecules and solving problems on E2\, E1\, and E1cB eliminati
 on reactions.
DURATION:PT1H
DTSTAMP:20240523T113535Z
DTSTART;TZID=America/New_York:20240614T110000
LAST-MODIFIED:20240523T113535Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Elucidating the role of metal-protein and metal-peptide interactio
 ns in microbial cellular stress
UID:CAL-8a008ae5-8f05e4c1-018f-a53bede8-00007994demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Conference_Symposium:/user/p
 ublic-user/Lectures_Conferences/Conference_Symposium
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:1620
X-BEDEWORK-IMAGE-Y2:1080
X-BEDEWORK-IMAGE-CROP-WIDTH:1620
X-BEDEWORK-IMAGE-CROP-HEIGHT:1080
X-BEDEWORK-SUBMITTEDBY:cd111 for Chemistry (agrp_ArtsandSciences_Chemistry
 )
X-BEDEWORK-IMAGE-ALT-TEXT:Ph.D. Defense- Outlaw\, Taylor
X-BEDEWORK-SPEAKER:Taylor Outlaw\, Ph.D. Candidate
X-BEDEWORK-IMAGE:/public/Images/GRAD-Outlaw\,Taylor-06-14-24_2024052311351
 8AM.jpg
X-BEDEWORK-THUMB-IMAGE:/public/Images/GRAD-Outlaw\,Taylor-06-14-24_2024052
 3113518AM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:My group is invested in the development of machine learning me
 thodology with applications in health and disease. Currently we are mostl
 y interested in leveraging representation learning and deep learning arch
 itectures to build models to represent data from different modalities suc
 h as longitudinal structured data (e.g.\, electronic health records)\, im
 ages (e.g.\, tomography\, ultrasound) and natural language (clinical narr
 ative)\, to be used in predictive tasks of relevance in healthcare. For i
 nstance\, classification or estimation of risk in diverse clinical outcom
 es\, and to address challenges associated with performance characterizati
 on in predictive models.
DURATION:PT1H
DTSTAMP:20240829T191011Z
DTSTART;TZID=America/New_York:20240909T120000
LAST-MODIFIED:20240829T191011Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Applications of Deep Learning in Healthcare
UID:CAL-8a00048d-91324965-0191-9f8ab2c5-00002a28demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
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 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_Schoolo
 fMedicine_BiostatisticsandBioinformatics,/principals/users/agrp_Centerfor
 GenomicandComputationalBiology,/principals/users/agrp_AGPM_Collaboratory,
 /principals/users/agrp_SchoolofMedicine,":Biostatistics and Bioinformatic
 s\,Duke Center for Genomic and Computational Biology (GCB)\,Precision Gen
 omics Collaboratory\,School of Medicine (SOM)
X-BEDEWORK-SPEAKER:Ricardo Henao
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
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X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Ricardo Henao\, PhD\, Associate Professor\, Depa
 rtment of Biostatistics and Bioinformatics\, Duke University
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Ricardo Henao canva_20240829070912PM.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Ricardo Henao canva_20240829070912PM
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END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:I admit the title intentionally overstates the case. But many 
 (most?) high-throughput biology datasets are based on aggregates\, where 
 aggregation occurs during either the experiment or data post-processing. 
 As a result\, any node in a graphical model of the data (e.g.\, Bayes net
 \, dynamic Bayes net\, Markov net\, point process\, or CRF) really is an 
 aggregate of many idealized single-measurement nodes\, so the real model 
 can be viewed as a high-dimensional tree-structured graphical model. We p
 rove that such models correspond to neural networks\, and also that every
  neural network can be viewed as such a model. Based on this theoretical 
 result\, we discuss potential applications\, including causal neural netw
 orks and the potential for a future "foundation model" for health. We als
 o use examples from clinical data (such as EHRs) in addition to biologica
 l data.
DURATION:PT1H
DTSTAMP:20240905T164905Z
DTSTART;TZID=America/New_York:20240916T120000
LAST-MODIFIED:20240905T164905Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Deep Neural Networks Really Are the Right Way for a Biostatisticia
 n to Analyze Biological Data or: How I Learned to Stop Worrying and Love 
 the DNN
UID:CAL-8a00048d-91324965-0191-c3159cee-000045b5demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_Schoolo
 fMedicine_BiostatisticsandBioinformatics,/principals/users/agrp_Centerfor
 GenomicandComputationalBiology,/principals/users/agrp_AGPM_Collaboratory,
 /principals/users/agrp_SchoolofMedicine,":Biostatistics and Bioinformatic
 s\,Duke Center for Genomic and Computational Biology (GCB)\,Precision Gen
 omics Collaboratory\,School of Medicine (SOM)
X-BEDEWORK-SPEAKER:David Page
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:David Page\, PhD\, JB Duke Professor and Chair o
 f the Department of Biostatistics &amp\;amp\; Bioinformatics at Duke Univ
 ersity
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/David Page canva photo_20240905044738PM.pn
 g
X-BEDEWORK-THUMB-IMAGE:/public/Images/David Page canva photo_2024090504473
 8PM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:Our lab primarily focuses on mammalian olfaction\, pioneering 
 the functional elucidation of odorant receptors. Our work includes large-
 scale characterization of odorant receptors and investigating human genet
 ic variations affecting odor perception. We have developed RNA sequencing
 -based techniques for identifying activated odorant receptors in behaving
  mice. Recently\, we contributed in resolving the first atomic structure 
 of a mammalian odorant receptor\, advancing understanding of odorant bind
 ing and activation mechanisms.
DURATION:PT1H
DTSTAMP:20240919T201735Z
DTSTART;TZID=America/New_York:20240923T120000
LAST-MODIFIED:20240919T201735Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Deciphering Odor Recognition
UID:CAL-8a00048d-91324965-0191-dce22fd3-00005fa9demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_Schoolo
 fMedicine_BiostatisticsandBioinformatics,/principals/users/agrp_Centerfor
 GenomicandComputationalBiology,/principals/users/agrp_AGPM_Collaboratory,
 /principals/users/agrp_SchoolofMedicine,":Biostatistics and Bioinformatic
 s\,Duke Center for Genomic and Computational Biology (GCB)\,Precision Gen
 omics Collaboratory\,School of Medicine (SOM)
X-BEDEWORK-SPEAKER:Hiro Matsunami
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:-0.3333333333333144
X-BEDEWORK-IMAGE-X2:530
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:530
X-BEDEWORK-IMAGE-CROP-HEIGHT:353.3333333333333
X-BEDEWORK-IMAGE-ALT-TEXT:Hiro Matsunami\, PhD\, Professor of Molecular Ge
 netics and Microbiology\, Duke University
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Hiro Matsunami canva photo_20240919081735P
 M.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Hiro Matsunami canva photo_202409190
 81735PM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:We are a diverse set of engineers and scientists solving healt
 h problems by using and developing systems biology tools and technologies
  to describe and control spatial relationships between cells in tissues. 
 While our primary goals of cellular organization are broad\, as are our c
 ollaborations\, we are particularly interested in applications involving 
 cell-based therapies.
DURATION:PT1H
DTSTAMP:20240919T202036Z
DTSTART;TZID=America/New_York:20240930T120000
LAST-MODIFIED:20240919T202036Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:From Pixels to Pathways: Computational Connection of Molecules to 
 Multicell Modules
UID:CAL-8a00048d-91324965-0192-0bf13874-00005fcfdemobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_PrattSc
 hool_BME,/principals/users/agrp_SchoolofMedicine_BiostatisticsandBioinfor
 matics,/principals/users/agrp_CenterforGenomicandComputationalBiology,/pr
 incipals/users/agrp_AGPM_Collaboratory,/principals/users/agrp_SchoolofMed
 icine,":Biomedical Engineering (BME)\,Biostatistics and Bioinformatics\,D
 uke Center for Genomic and Computational Biology (GCB)\,Precision Genomic
 s Collaboratory\,School of Medicine (SOM)
X-BEDEWORK-SPEAKER:John Hickey
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Dr. John Hickey\, PhD\, Assistant Professor in B
 iomedical Engineering at Duke University
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/John Hickey canva  photo_20240919082010PM.
 png
X-BEDEWORK-THUMB-IMAGE:/public/Images/John Hickey canva  photo_20240919082
 010PM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:In 2016\, The Department of Veterans Affairs (VA) and the Depa
 rtment of Energy (DOE) have established an Interagency Agreement (IAA) to
  combine VA's vast array of clinical and genomic data with DOE's national
  computing capabilities-including the most powerful supercomputer in the 
 nation-to push the frontiers of precision medicine to support the Preside
 nt's National Precision Medicine Initiative (PMI) and improve the lives a
 nd wellbeing of the nation's veterans. Guided by the vision to improve th
 e health and wellbeing of the nation's veterans and the general public\, 
 the MVP Champion (Computational Health Analytics for Medical Precision to
  Improve Outcomes Now) program will develop better methods to treat\, cur
 e\, detect at early stages\, and prevent diseases through precision medic
 ine by harnessing the genomic and clinical data in the VA's Million Veter
 an Program (MVP) and the computational power within the DOE. In this talk
 \, we will present results from this project that led to creation of new 
 computational methods that scaled to both the genetics data and computati
 onal capabilities that are made available for this project. We will espec
 ially\, focus on the genome-wide PheWAS study\, where we performed 300 bi
 llion association studies on more than half of DOE's supercomputer called
  Summit\, accelerating the analysis pipeline 100 fold over current state 
 of the art resulting in discovery of over 38K novel biomarkers [1]. Addit
 ionally\, we will present ongoing work on developing AI/ML technologies f
 or disease risk prediction\, diagnosis and treatment.
DURATION:PT1H
DTSTAMP:20240927T173624Z
DTSTART;TZID=America/New_York:20241007T120000
LAST-MODIFIED:20240927T173624Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Leveraging High Performance Computing and AI to Advance Biomedical
  Discovery
UID:CAL-8a00048d-91324965-0192-348d7cfd-00006172demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_PrattSc
 hool_BME,/principals/users/agrp_SchoolofMedicine_BiostatisticsandBioinfor
 matics,/principals/users/agrp_CenterforGenomicandComputationalBiology,/pr
 incipals/users/agrp_AGPM_Collaboratory,/principals/users/agrp_SchoolofMed
 icine,":Biomedical Engineering (BME)\,Biostatistics and Bioinformatics\,D
 uke Center for Genomic and Computational Biology (GCB)\,Precision Genomic
 s Collaboratory\,School of Medicine (SOM)
X-BEDEWORK-SPEAKER:Ravi Madduri
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Dr. Ravi Madduri\, PhD\, Senior Computer Scienti
 st\, Argonne National Laboratory
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Ravi Madduri canva photo_20240927053540PM.
 png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Ravi Madduri canva photo_20240927053
 540PM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:Electronic health records (EHRs) have immense potential to tra
 nsform medicine both at the point-of-care and through retrospective resea
 rch. However\, current EHRs are burdensome to use\, resulting in document
 ation which is suboptimal for patients\, clinicians\, and researchers ali
 ke. Clinical notes are written in their own jargon-heavy dialect\, patien
 t histories can contain hundreds of notes\, and there is often minimal la
 beled data available. In this talk\, I will first discuss scalable techni
 ques for clinical information extraction that leverage large language mod
 els\, how these methods could improve equity in healthcare\, and how we m
 ight think about the data training these models. Next\, I will describe a
  paradigm for smarter electronic health records that decreases documentat
 ion burden\, incentivizes the creation of high-quality data at the point-
 of-care\, and aids in information retrieval. I will also briefly describe
  work exploring clinical text summarization and medical text simplificati
 on. I will end with open challenges and opportunities for NLP to impact a
  variety of healthcare workflows\, with a lens towards human-AI interacti
 on\, evaluation\, and deployability.
DURATION:PT1H
DTSTAMP:20241004T205756Z
DTSTART;TZID=America/New_York:20241021T120000
LAST-MODIFIED:20241004T205756Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Scalable Natural Language Processing to Transform Healthcare
UID:CAL-8a00048d-91324965-0192-5952c6e1-00002507demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_PrattSc
 hool_BME,/principals/users/agrp_SchoolofMedicine_BiostatisticsandBioinfor
 matics,/principals/users/agrp_CenterforGenomicandComputationalBiology,/pr
 incipals/users/agrp_AGPM_Collaboratory,/principals/users/agrp_SchoolofMed
 icine,":Biomedical Engineering (BME)\,Biostatistics and Bioinformatics\,D
 uke Center for Genomic and Computational Biology (GCB)\,Precision Genomic
 s Collaboratory\,School of Medicine (SOM)
X-BEDEWORK-SPEAKER:Monica Agrawal
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Dr. Monica Agrawal\, PhD\, Assistant Professor i
 n the Biostatistics and Bioinformatics department at Duke
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Monica Agrawal canva photo_20241004085729P
 M.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Monica Agrawal canva photo_202410040
 85729PM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:Early autism screening is an important part of pediatric prima
 ry care that can help direct children into services. Currently\, most aut
 ism screening is conducted via the M-Chat\, a provider administered quest
 ionnaire. While useful\, the M-Chat is prone to inconsistent and misuse. 
 Epidemiologic work has shown that autistic children have early life clini
 cal experiences that can be indicative of a future autism diagnosis. Such
  encounter data can be used to promote an automated\, health system based
 \, screening tool. Nonetheless\, predicting a future autism diagnosis is 
 challenging due to the rarity and complexity of the outcome. In this talk
 \, I discuss a variety of ways we are working to improve a machine learni
 ng based prediction model for autism. We touch on topics of data represen
 tation\, borrowing from related conditions & data sources\, and addressin
 g algorithmic bias.
DURATION:PT1H
DTSTAMP:20241023T234952Z
DTSTART;TZID=America/New_York:20241028T120000
LAST-MODIFIED:20241023T234952Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:One Step at a Time: Exploring Multiple Ways to Improve a Machine L
 earning Model to Predict a Future Autism Diagnosis
UID:CAL-8a00048d-91324965-0192-904673e6-0000075ddemobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_SOM_For
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 ,/principals/users/agrp_CenterforGenomicandComputationalBiology,/principa
 ls/users/agrp_DCRI,/principals/users/agrp_SchoolofMedicine_PopulationHeal
 thSciences,/principals/users/agrp_AGPM_Collaboratory,/principals/users/ag
 rp_SchoolofMedicine,":AI Health\,Biostatistics and Bioinformatics\,Duke C
 enter for Genomic and Computational Biology (GCB)\,Duke Clinical Research
  Institute (DCRI)\,Population Health Sciences\,Precision Genomics Collabo
 ratory\,School of Medicine (SOM)
X-BEDEWORK-SPEAKER:Ben Goldstein
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Pictured is Dr. Ben Goldstein\, a man with light
  skin short black hair\, smiling and wearing a maroon and white striped p
 olo shirt
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Ben Goldstein canva photo_20241015010833PM
 .png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Ben Goldstein canva photo_2024101501
 0833PM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:A significant challenge in vaccine design is the elicitation o
 f broadly-neutralizing antibodies (bnAbs) to protect against viral escape
 . We are developing computational models of affinity maturation to unders
 tand bottlenecks in the inducibility of bnAbs and guide sequential vaccin
 e strategies. Doing so requires accounting for context-dependence in soma
 tic hypermutation\, which in turn requires phylogenetic inference in the 
 presence of site-dependence\, a long-standing challenge in computational 
 biology. We describe an approximation algorithm for this problem using a 
 combined data-augmentation and importance sampling scheme. We apply this 
 approach to reconstruct maturation lineages from high-throughput B cell r
 eceptor repertoire sequencing data\, and examine the impact of context-de
 pendence on reconstruction accuracy. We then apply our models to the prob
 lem of choosing targets for the design of boosting immunogens aimed at el
 icitation of HIV bnAbs.
DURATION:PT1H
DTSTAMP:20241023T235317Z
DTSTART;TZID=America/New_York:20241104T120000
LAST-MODIFIED:20241023T235317Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Randomized Algorithms\, Bayesian Phylogenetics\, and Computational
  Vaccine Design
UID:CAL-8a00048d-91324965-0192-bb0754df-0000448cdemobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_SOM_For
 ge,/principals/users/agrp_SchoolofMedicine_BiostatisticsandBioinformatics
 ,/principals/users/agrp_SchoolofMedicine_StatGen,/principals/users/agrp_C
 enterforGenomicandComputationalBiology,/principals/users/agrp_SchoolofMed
 icine_PopulationHealthSciences,/principals/users/agrp_SchoolofMedicine,/p
 rincipals/users/agrp_StatisticalScience,":AI Health\,Biostatistics and Bi
 oinformatics\,Center for Statistical Genetics and Genomics (StatGen)\,Duk
 e Center for Genomic and Computational Biology (GCB)\,Population Health S
 ciences\,School of Medicine (SOM)\,Statistical Science
X-BEDEWORK-SPEAKER:Scott Schmidler
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Pictured is Dr. Scott Schmidler a man with short
  dark brown hair light skin and blue eyes smiling. He is wearing a light-
 colored collared shirt
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Scott Schmidler canva photo_20241023081752
 PM.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Scott Schmidler canva photo_20241023
 081752PM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:The CRISPR toolbox allows functional interrogation of the geno
 me in the service of three foundational questions: 1) What genes are invo
 lved in my phenotype of interest? 2) How does function arise from a genet
 ic locus? 3) How do genes interact to produce a phenotype? The Genetic Pe
 rturbation Platform (GPP) at the Broad Institute engages in dozens of col
 laborative screening projects each year\, and is also the home for >1\,70
 0 genetic screens reported in the Cancer Dependency Map (DepMap). We thus
  aim to continually incorporate new technologies and best practices in se
 rvice of these questions\, whether derived in-house or learned from the l
 iterature\, quickly and at scale. Here\, we will describe advances to our
  screening strategies across numerous CRISPR technologies\, including kno
 ckout\, activation\, interference\, and base editing.
DURATION:PT1H
DTSTAMP:20241101T002659Z
DTSTART;TZID=America/New_York:20241118T120000
LAST-MODIFIED:20241101T002659Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Where Does He Get Those Wonderful Toys?  A Tour of the Functional 
 Genomics Toolbox
UID:CAL-8a000483-92c3adf6-0192-e51dd58e-00001198demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_Schoolo
 fMedicine_BiostatisticsandBioinformatics,/principals/users/agrp_Pratt_CAG
 T,/principals/users/agrp_SchoolofMedicine_DSCB,/principals/users/agrp_Cen
 terforGenomicandComputationalBiology,/principals/users/agrp_SchoolofMedic
 ine_MolecularGenetics,/principals/users/agrp_SchoolofMedicine,/principals
 /users/agrp_SchoolofMedicine_UPGG,":Biostatistics and Bioinformatics\,Cen
 ter for Advanced Genomic Technologies\,Developmental and Stem Cell Biolog
 y Program\,Duke Center for Genomic and Computational Biology (GCB)\,Molec
 ular Genetics and Microbiology (MGM)\,School of Medicine (SOM)\,Universit
 y Program in Genetics &amp\;amp\; Genomics (UPGG)
X-BEDEWORK-SPEAKER:John Doench
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Pictured is Dr. John Doench a man with short dar
 k brown hair light skin wearing glasses and smiling. He is wearing a whit
 e button up collared shirt.
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/John Doench canva photo_20241101122630AM.p
 ng
X-BEDEWORK-THUMB-IMAGE:/public/Images/John Doench canva photo_202411011226
 30AM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:Advent of single-cell genomics has enhanced our ability to stu
 dy heterogeneous cell populations (1) to track course of temporal process
 es\, such as cellular differentiation\, (2) to identify novel and rare ce
 ll states\, and (3) characterize the heterogeneity of complex tissues\, s
 uch as tumors. In this talk\, I will present three methods to study such 
 cell populations using multimodal single-cell omics assays. Our first alg
 orithm\, Epiconfig\, is an interpretable multimodal topic model that lear
 ns unsupervised clustering of single-cells while modeling cross modality 
 relationships. We applied EpiConfig to a collection of sc-RNA+ATAC-seq as
 says that jointly measure transcriptomic and chromatin accessibility of s
 ingle cells from healthy and cancerous cell populations. Epi-Config is as
  accurate as widely used sc-multiomics clustering methods\; it learns set
 s of unimodal and cross modality features\, called topics\, that correspo
 nd to specific cell types and states. We developed a shiny app for interp
 retation of these topics to obtain biological insights into different cel
 l states\; we show that cross modality features reflect 3D genome interac
 tions. Our second method\, RIDDLER\, can identify copy number variation (
 CNV) events in single-cell datasets. CNV is a widely studied type of geno
 mic structural variation that can have direct and indirect effects on gen
 e dosage\, and may drive cancer progression. RIDDLER is a single-cell res
 olution CNV detection algorithm based on outlier aware generalized linear
  modeling. We demonstrate the effectiveness of our algorithm on cancer ce
 ll line models where it achieves better agreement with sc-WGS derived CNV
 s than competing methods. RIDDLER is able to accurately reconstruct clona
 l heterogeneity of the cell population\, in accordance with sc-WGS derive
 d clones\, and can be applied to both sc-ATAC-seq\, sc-WGS and sc-methyla
 tion datasets. Lastly\, I will introduce scPrePrint\, an algorithm for st
 udying transcription factor (TF) binding to chromatin using sc-ATAC-seq d
 ata. scPrePrint uses an unsupervised deep neural network to identify tran
 scription factor binding sites via modeling of the ATAC footprint left on
  the TF binding site\; while correcting for ATAC sequence bias. We deploy
 ed scPrePrint on publicly available sc-ATAC-seq from cell lines\, and sho
 w that our footprint calls are concordant with ChIP-seq data.
DURATION:PT1H
DTSTAMP:20241116T012600Z
DTSTART;TZID=America/New_York:20241125T120000
LAST-MODIFIED:20241116T012600Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Multimodal Characterization of Cell States at Single-Cell Resoluti
 on
UID:CAL-8a000483-92c3adf6-0193-32932587-0000430edemobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_Schoolo
 fMedicine_BiostatisticsandBioinformatics,/principals/users/agrp_Pratt_CAG
 T,/principals/users/agrp_SchoolofMedicine_DSCB,/principals/users/agrp_Cen
 terforGenomicandComputationalBiology,/principals/users/agrp_SchoolofMedic
 ine_MolecularGenetics,/principals/users/agrp_SchoolofMedicine,/principals
 /users/agrp_SchoolofMedicine_UPGG,":Biostatistics and Bioinformatics\,Cen
 ter for Advanced Genomic Technologies\,Developmental and Stem Cell Biolog
 y Program\,Duke Center for Genomic and Computational Biology (GCB)\,Molec
 ular Genetics and Microbiology (MGM)\,School of Medicine (SOM)\,Universit
 y Program in Genetics &amp\;amp\;amp\;amp\;amp\; Genomics (UPGG)
X-BEDEWORK-SPEAKER:Gurkan Yardimci
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Pictured is Dr. Gurkan Yardimci a man with short
  dark brown hair light skin. He is wearing a dark shirt.
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Gurkan Yardimci canva photo_20241116012524
 AM.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Gurkan Yardimci canva photo_20241116
 012524AM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=00f1fcdb-0f068baf-010f-068baf83-00000004:None
CREATED:20241122T182316Z
DESCRIPTION:The Department of Chemistry is pleased to host Dr. Gregory Cra
 ven for a seminar on Monday\, December 2. \n\nTitle: "Mutant-selective AK
 T1 inhibition via lysine targeting and neo-zinc chelation"\n\nAbstract: M
 utations in the kinase AKT1\, especially the E17K mutation\, drive oncoge
 nic signaling in many solid tumors. In clinical studies\, pan-AKT inhibit
 ors cause dose-limiting hyperglycemia\, motivating the search for mutant-
 selective inhibitors. To address this\, I exploited the E17K mutation to 
 design allosteric\, lysine-targeted salicylaldehyde inhibitors with selec
 tivity for AKT1(E17K) over wild type AKT paralogs\, a major challenge giv
 en the presence of three conserved lysines near the allosteric site. Stru
 ctural studies revealed an unexpected mode of covalent inhibition involvi
 ng neo-zinc coordination\, which drives exceptional selectivity and resid
 ence-time in cellular models and tumor xenografts. This approach opens a 
 pathway for the selective targeting of other oncogenic lysine mutations i
 n cancer and motivates the search for new pharmacological opportunities b
 y exploiting ligand-induced metal chelation.\n\nHost: Chemistry Departmen
 t Chemical Biology Series
DURATION:PT1H
DTSTAMP:20241122T182752Z
DTSTART;TZID=America/New_York:20241202T114500
LAST-MODIFIED:20241122T182752Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Chemistry Seminar Presented by Dr. Gregory Craven
UID:CAL-8a000483-92c3adf6-0193-551d30bf-0000562cdemobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-STUDENT-CONTACT;X-BEDEWORK-PARAM-EMAIL=c.conti@duke.edu:Departm
 ent of Chemistry
X-BEDEWORK-SPEAKER:Dr. Gregory Craven\, University of California San Franc
 isco
X-BEDEWORK-DUKE-SERIES:Chemistry Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:234
X-BEDEWORK-IMAGE-X2:1236
X-BEDEWORK-IMAGE-Y2:1058
X-BEDEWORK-IMAGE-CROP-WIDTH:1236
X-BEDEWORK-IMAGE-CROP-HEIGHT:824
X-BEDEWORK-IMAGE-ALT-TEXT:Researcher stands in red shirt in outdoor settin
 g
X-BEDEWORK-SUBMITTEDBY:cconti for Chemistry (agrp_ArtsandSciences_Chemistr
 y)
X-BEDEWORK-IMAGE:/public/Images/Gregory Craven2_20241122062316PM.jpg
X-BEDEWORK-THUMB-IMAGE:/public/Images/Gregory Craven2_20241122062316PM-thu
 mb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=00f1fcdb-0f068baf-010f-068baf83-00000004:None
CREATED:20241125T153118Z
DESCRIPTION:The Department of Chemistry is pleased to host Dr. Evert Njome
 n for a seminar on Monday\, December 9. \n\nTitle: "Targeting the Undrugg
 ed Proteome with Small Molecules"\n\nAbstract: Human genetics has greatly
  enhanced our understanding of the fraction of human proteins and their p
 roteoforms with disease relevance. However\, many of these proteins remai
 n uncharacterized and lack selective small-molecule ligands to decipher t
 heir role in human pathophysiology. Understanding how these proteins cont
 ribute to human diseases and how we can develop safer therapeutic strateg
 ies to address them remains a significant challenge at the interface of c
 hemistry and biology. This seminar will focus on small molecule approache
 s to discover and characterize proteins that contribute to human diseases
 \, including cancer. Emphasis will be placed on an integrated chemical pr
 oteomic platform for proteome-wide ligand discovery in native biological 
 systems. I will discuss how this integrated approach has enabled the disc
 overy and characterization of ligands for structurally and functionally d
 iverse proteins. This includes compounds that stereoselectively and site-
 specifically disrupt the spindle assembly checkpoint complex\, leading to
  delayed mitotic exit in cancer cells\, as well as the broader applicatio
 ns of this platform.\n\nHost: Chemistry Department Chemical Biology Serie
 s
DURATION:PT1H
DTSTAMP:20241127T203131Z
DTSTART;TZID=America/New_York:20241209T121500
LAST-MODIFIED:20241127T203131Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Chemistry Seminar Presented by Dr. Evert Njomen
UID:CAL-8a000483-92c3adf6-0193-63f2d6ba-00006df0demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-STUDENT-CONTACT;X-BEDEWORK-PARAM-EMAIL=c.conti@duke.edu:Departm
 ent of Chemistry
X-BEDEWORK-SPEAKER:Dr. Evert Njomen\, Scripps Research Institute
X-BEDEWORK-DUKE-SERIES:Chemistry Department Seminar
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:75
X-BEDEWORK-IMAGE-X2:657
X-BEDEWORK-IMAGE-Y2:513
X-BEDEWORK-IMAGE-CROP-WIDTH:657
X-BEDEWORK-IMAGE-CROP-HEIGHT:438
X-BEDEWORK-IMAGE-ALT-TEXT:Researcher in grey plaid jacket sits in a chemis
 try lab
X-BEDEWORK-SUBMITTEDBY:cconti for Chemistry (agrp_ArtsandSciences_Chemistr
 y)
X-BEDEWORK-IMAGE:/public/Images/Headshot_Njomen_20241125033119PM.jpg
X-BEDEWORK-THUMB-IMAGE:/public/Images/Headshot_Njomen_20241125033119PM-thu
 mb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=00f1fcdb-0f068baf-010f-068baf83-00000004:None
CREATED:20241127T044538Z
DESCRIPTION:The Department of Chemistry is pleased to host Dr. Carly Schis
 sel for a seminar on Wednesday\, December 11.\n\nTitle: "Strategies to Di
 scover\, Design\, and Synthesize Unnatural Bioactive Peptides"\n\nAbstrac
 t: Peptide therapeutics are a rapidly expanding frontier in drug developm
 ent. New methods that address challenges in the discovery\, design\, and 
 synthesis of bioactive peptides are needed to advance these molecules as 
 medicines. One of the most important roadblocks that macromolecular drugs
  face is their inability to reach intracellular targets. I will demonstra
 te new approaches for the design and synthesis of unnatural bioactive pep
 tides. First\, we used machine learning for the de novo design of nuclear
 -targeting miniproteins to traffic macromolecular cargo to the nucleus of
  cells. We found that the model was able to predict new sequences with ac
 tivities extrapolated beyond the training dataset\, resulting in the most
  active variants yet. Next\, we demonstrated a method for in-cell penetra
 tion selection-mass spectrometry to discover cytosol-targeting peptides f
 rom a synthetic library. Novel unnatural sequences found from the cytosol
  trafficked oligonucleotide cargo to the nucleus better than those found 
 in whole cell extracts. A key outcome of these efforts was that the prese
 nce of unnatural amino acids with extended backbones conferred enhanced b
 ioactivity. The ribosomal synthesis of proteins and peptides with unnatur
 al peptide backbones is thus of critical importance. In the second part o
 f the presentation\, we developed post-translational acyl shift reactions
  to install internal diketones\, heterocycles\, and extended backbones in
  ribosomal peptides and proteins. These works advance the therapeutic pot
 ential of peptides by both developing new bioactive sequences and enablin
 g their biological synthesis.\n\nHost: Chemistry Department Chemical Biol
 ogy Series
DURATION:PT1H
DTSTAMP:20241127T044538Z
DTSTART;TZID=America/New_York:20241211T121500
LAST-MODIFIED:20241127T044538Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Chemistry Seminar Presented by Dr. Carly Schissel
UID:CAL-8a000483-92c3adf6-0193-6bf06dca-00000fdedemobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-SPEAKER:Dr. Carly Schissel\, University of California\, Berkele
 y
X-BEDEWORK-DUKE-SERIES:Chemistry Seminar Series
X-BEDEWORK-STUDENT-CONTACT;X-BEDEWORK-PARAM-EMAIL=c.conti@duke.edu:Departm
 ent of Chemistry
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:123
X-BEDEWORK-IMAGE-X2:960
X-BEDEWORK-IMAGE-Y2:763
X-BEDEWORK-IMAGE-CROP-WIDTH:960
X-BEDEWORK-IMAGE-CROP-HEIGHT:640
X-BEDEWORK-IMAGE-ALT-TEXT:Researcher stands in a black and white polka dot
  shirt in glasses against a concrete wall
X-BEDEWORK-SUBMITTEDBY:cconti for Chemistry (agrp_ArtsandSciences_Chemistr
 y)
X-BEDEWORK-IMAGE:/public/Images/Schissel_20241127044538AM.jpg
X-BEDEWORK-THUMB-IMAGE:/public/Images/Schissel_20241127044538AM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=00f1fcdb-0f068baf-010f-068baf83-00000004:None
CREATED:20241125T153638Z
DESCRIPTION:The Department of Chemistry is pleased to host Dr. Nicholas Ti
 ll for a seminar on Friday\, December 13. \n\nTitle: "Mechanistic Investi
 gation of Nickel/Photoredox Catalysis and Redirecting Trogocytosis for Ta
 rgeted Protein Transfer"\n\nAbstract: Part I: Visible light photoredox ca
 talysis is a powerful method to modulate small molecule and transition me
 tal reactivity\, but we lack insight into the mechanistic basis of this t
 echnology. I will present a comprehensive study of an industrially import
 ant Nickel/photoredox catalyzed C-N cross-coupling reaction. Using a comb
 ination of reaction kinetic analysis\, ultrafast spectroscopy\, and stoic
 hiometric organometallic studies\, we elucidate the key steps in the mech
 anism of this reaction. We then leverage these insights to design a new p
 hotocatalyst yielding improved reaction rate (>30-fold) and quantum yield
  (>10-fold).\n\nPart II: Targeted degradation of cell surface proteins ca
 n address therapeutic challenges rooted in pathologic over-expression or 
 over-activation of a disease-driving protein. Directly introducing cell s
 urface proteins to address therapeutic challenges rooted in pathologic pr
 otein deficiency or dysfunction remains an unsolved challenge. I will pre
 sent the development of bispecific molecules (TrogoTACs) capable of induc
 ing contactdependent protein transfer between cells by redirecting trogoc
 ytosis in a targeted fashion. To accomplish this goal\, we designed chime
 ric antibody-small molecule conjugates with specificity to cell surface p
 roteins displaying mutually exclusive expression on donor and acceptor ce
 ll types. The protein transfer process is rapid\, requires cell-cell cont
 act\, and depends on expression of the receptors targeted by the TrogoTAC
 . Transferred proteins can then redirect T cell engager cytotoxicity to r
 ewire therapeutic targeting towards\notherwise unresponsive cancer cells.
 \n\nHost: Chemistry Department Chemical Biology Series
DURATION:PT1H
DTSTAMP:20241125T153638Z
DTSTART;TZID=America/New_York:20241213T121500
LAST-MODIFIED:20241125T153638Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Chemistry Seminar Presented by Dr. Nicholas Till
UID:CAL-8a000483-92c3adf6-0193-63f7b542-00006eb2demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-SPEAKER:Dr. Nicholas Till\, Stanford University
X-BEDEWORK-DUKE-SERIES:Department of Chemistry Seminar
X-BEDEWORK-STUDENT-CONTACT;X-BEDEWORK-PARAM-EMAIL=c.conti@duke.edu:Departm
 ent of Chemistry
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:138
X-BEDEWORK-IMAGE-X2:1498
X-BEDEWORK-IMAGE-Y2:1136.6666666666665
X-BEDEWORK-IMAGE-CROP-WIDTH:1498
X-BEDEWORK-IMAGE-CROP-HEIGHT:998.6666666666665
X-BEDEWORK-IMAGE-ALT-TEXT:Researcher stands in a navy blue jacket and ligh
 t blue shirt in an outdoor setting
X-BEDEWORK-SUBMITTEDBY:cconti for Chemistry (agrp_ArtsandSciences_Chemistr
 y)
X-BEDEWORK-IMAGE:/public/Images/nick3_20241125033638PM.jpeg
X-BEDEWORK-THUMB-IMAGE:/public/Images/nick3_20241125033638PM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=00f1fcdb-0f068baf-010f-068baf83-00000004:None
CREATED:20241206T204755Z
DESCRIPTION:The Department of Chemistry is pleased to host Dr. Zhe Zhuang 
 for a seminar on Monday\, December 16. \n\nTitle: "Molecular Glue Discove
 ry Enabled by Targeted Degron Display"\n\nAbstract: Small molecules that 
 induce protein interactions hold tremendous potential as new medicines\, 
 as probes for molecular pathways\, and as tools for agriculture. Explosiv
 e growth of targeted protein degradation drug development has spurred ren
 ewed interest in proximity inducing molecules and especially molecular gl
 ue degraders. These compounds catalyze destruction of disease-causing pro
 teins by reshaping protein surfaces and promoting cooperative binding bet
 ween ubiquitylating enzymes and target proteins. Molecular glue discovery
  for pre-defined targets is a major challenge in contemporary drug discov
 ery. Here I will discuss how we address these important chemical challeng
 es through molecular glue discovery enabled by targeted degron display. B
 y leveraging mechanisms such as electrophilic covalent bonding\, electros
 tatic interactions\, or cation-pi interactions\, I have identified a rang
 e of potent molecular glue degraders that recruit previously unligandable
  ubiquitylating factors for multiple therapeutically relevant epigenetic 
 regulators and kinases. This "chemocentric" approach provides a powerful 
 strategy to discover molecular glues that induce proximity to ubiquitin l
 igases with similarly desirable properties.\n\nHost: Chemistry Department
  Chemical Biology Series
DURATION:PT1H
DTSTAMP:20241206T204755Z
DTSTART;TZID=America/New_York:20241216T121500
LAST-MODIFIED:20241206T204755Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Chemistry Seminar Presented by Dr. Zhe Zhuang
UID:CAL-8a000483-92c3adf6-0193-9dbaa6eb-00004c80demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-SPEAKER:Dr. Zhe Zhuang\, Stanford University
X-BEDEWORK-DUKE-SERIES:Chemistry Seminar Series
X-BEDEWORK-STUDENT-CONTACT;X-BEDEWORK-PARAM-EMAIL=c.conti@duke.edu:Chemist
 ry Department
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:434
X-BEDEWORK-IMAGE-X2:2304
X-BEDEWORK-IMAGE-Y2:1970
X-BEDEWORK-IMAGE-CROP-WIDTH:2304
X-BEDEWORK-IMAGE-CROP-HEIGHT:1536
X-BEDEWORK-IMAGE-ALT-TEXT:Researcher with dark framed glasses stands in a 
 grey suit
X-BEDEWORK-SUBMITTEDBY:cconti for Chemistry (agrp_ArtsandSciences_Chemistr
 y)
X-BEDEWORK-IMAGE:/public/Images/photo-Zhe Zhuang_20241206084755PM.jpeg
X-BEDEWORK-THUMB-IMAGE:/public/Images/photo-Zhe Zhuang_20241206084755PM-th
 umb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:The Love lab develops statistical methods and open source soft
 ware for analysis of high dimensional biological data. We collaborate wit
 h groups in Genetics\, Biology\, Computer Science\, Neuroscience/Psychiat
 ry\, and Cancer Epidemiology\, to improve data analysis tools and workflo
 ws\, with a focus on transcriptomics. Here I will talk about updates from
  an international team within R/Bioconductor working to enable tidy data 
 analysis for complex objects\, such as genome annotations or single cell 
 expression sets.
DURATION:PT1H
DTSTAMP:20250110T213416Z
DTSTART;TZID=America/New_York:20250127T120000
LAST-MODIFIED:20250110T213416Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Tidyomics: Enabling Tidy Data Analysis Workflows for Complex Biolo
 gical Data
UID:CAL-8a000483-92c3adf6-0194-52199a7b-000001b7demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_Schoolo
 fMedicine_BiostatisticsandBioinformatics,/principals/users/agrp_Pratt_CAG
 T,/principals/users/agrp_CenterforGenomicandComputationalBiology,/princip
 als/users/agrp_AGPM_Collaboratory,/principals/users/agrp_SchoolofMedicine
 ,/principals/users/agrp_SchoolofMedicine_UPGG,":Biostatistics and Bioinfo
 rmatics\,Center for Advanced Genomic Technologies\,Duke Center for Genomi
 c and Computational Biology (GCB)\,Precision Genomics Collaboratory\,Scho
 ol of Medicine (SOM)\,University Program in Genetics &amp\;amp\;amp\;amp\
 ;amp\;amp\;amp\;amp\; Genomics (UPGG)
X-BEDEWORK-SPEAKER:Mike Love\, PhD
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Pictured is Dr. Mike Love\, PhD\, a man with sho
 rt curly dark hair and a beard\, wearing glasses\, wearing a dark jacket 
 indoors with a softly lit background featuring windows and beige walls
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Mike Love canva photo_20250110092316PM.png
 
X-BEDEWORK-THUMB-IMAGE:/public/Images/Mike Love canva photo_20250110092316
 PM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:The Venturelli Lab aims to understand the molecular\, ecologic
 al and systems-level design\nprinciples of microbiomes and their interact
 ions with the environment and the host. The major goals of our research p
 rogram include developing the capability to predict their behaviors in re
 sponse to environmental perturbations and identify influential control kn
 obs for steering microbiomes to desired states. Our detailed and quantita
 tive understanding of the multiscale interactions shaping the human gut m
 icrobiome will guide the design\nof precision bacterial therapeutics and 
 dietary interventions with applications spanning infectious\, autoimmune 
 and metabolic diseases as well as manipulation of the gut-brain axis.
DURATION:PT1H
DTSTAMP:20250124T213124Z
DTSTART;TZID=America/New_York:20250203T120000
LAST-MODIFIED:20250124T213124Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Understanding and Engineering the Multi-Scale Dynamics and Functio
 ns Of Microbial Communities
UID:CAL-8a000483-92c3adf6-0194-9a39b064-00003309demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_PrattSc
 hool_BME,/principals/users/agrp_SchoolofMedicine_BiostatisticsandBioinfor
 matics,/principals/users/agrp_Pratt_CAGT,/principals/users/agrp_Centerfor
 GenomicandComputationalBiology,/principals/users/agrp_AGPM_Collaboratory,
 /principals/users/agrp_SchoolofMedicine,/principals/users/agrp_SchoolofMe
 dicine_UPGG,":Biomedical Engineering (BME)\,Biostatistics and Bioinformat
 ics\,Center for Advanced Genomic Technologies\,Duke Center for Genomic an
 d Computational Biology (GCB)\,Precision Genomics Collaboratory\,School o
 f Medicine (SOM)\,University Program in Genetics &amp\;amp\; Genomics (UP
 GG)
X-BEDEWORK-SPEAKER:Ophelia Venturelli\, PhD
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Pictured is Dr. Ophelia Venturelli\, PhD\, a wom
 an with shoulder-length dark brown hair smiling warmly at the camera. She
  is wearing a gray sweater over a pink top\, standing in front of a light
 -colored mesh background with soft lighting
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Ophelia Venturelli canva photo_20250124093
 059PM.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Ophelia Venturelli canva photo_20250
 124093059PM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:My research team leverages data science to tackle previously i
 ntractable questions about how social and chemical environmental factors 
 influence health and wellness. Equally important\, we collaborate with lo
 cal organizations and communities to effectively communicate environmenta
 l risks\, driving actionable solutions that reduce disease burden\, save 
 lives\, and enhance overall well-being.
DURATION:PT1H
DTSTAMP:20250201T013840Z
DTSTART;TZID=America/New_York:20250210T120000
LAST-MODIFIED:20250201T013840Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Understanding Environmental Health Effects Among the Most Vulnerab
 le Using Electronic Health Records and Molecular Data
UID:CAL-8a000483-92c3adf6-0194-bf27e326-000004bedemobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_PrattSc
 hool_BME,/principals/users/agrp_SchoolofMedicine_BiostatisticsandBioinfor
 matics,/principals/users/agrp_Pratt_CAGT,/principals/users/agrp_Centerfor
 GenomicandComputationalBiology,/principals/users/agrp_AGPM_Collaboratory,
 /principals/users/agrp_SchoolofMedicine,/principals/users/agrp_SchoolofMe
 dicine_UPGG,":Biomedical Engineering (BME)\,Biostatistics and Bioinformat
 ics\,Center for Advanced Genomic Technologies\,Duke Center for Genomic an
 d Computational Biology (GCB)\,Precision Genomics Collaboratory\,School o
 f Medicine (SOM)\,University Program in Genetics &amp\;amp\;amp\;amp\;amp
 \; Genomics (UPGG)
X-BEDEWORK-SPEAKER:Cavin Ward-Caviness\, PhD
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Pictured is Dr. Cavin Ward-Caviness\, PhD\, a sm
 iling man with dark skin\, long dark hair\, and a well-groomed beard. He 
 is wearing a black blazer over a striped dress shirt with a patterned col
 lar. The background is plain white.
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Cavin Ward-Caviness canva photo_2025020101
 3729AM.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Cavin Ward-Caviness canva photo_2025
 0201013729AM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:Evolution occurs when selective pressures from the environment
  shape inherited variation over time. Within the laboratory\, evolution i
 s commonly used to engineer proteins and RNA\, but experimental constrain
 ts have limited our ability to reproducibly and reliably explore key fact
 ors such as population diversity\, the timing of environmental changes\, 
 and chance. We developed a high-throughput system for the analytical expl
 oration of molecular evolution using phage-based mutagenesis to evolve ma
 ny distinct classes of biomolecules simultaneously. In this talk\, I will
  describe the development of our open-source python:robot integration pla
 tform which enables us to adjust the stringency of selection in response 
 to real-time evolving activity measurements and to dissect the historical
 \, environmental\, and random factors governing biomolecular evolution. F
 inally\, I will talk about our many ongoing and future projects which uti
 lize this system to evolve previously intractable biomolecules to target 
 the undruggable proteome of protein-protein interactions.
DURATION:PT1H
DTSTAMP:20250207T204229Z
DTSTART;TZID=America/New_York:20250217T120000
LAST-MODIFIED:20250207T204229Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Phage and Robotics-Assisted Directed Evolution
UID:CAL-8a000483-92c3adf6-0194-e22442db-00004178demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_PrattSc
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 /principals/users/agrp_SchoolofMedicine,/principals/users/agrp_SchoolofMe
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 \;amp\;amp\;amp\; Genomics (UPGG)
X-BEDEWORK-SPEAKER:Emma Chory\, PhD
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
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X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Pictured is Dr. Emma Chory\, PhD\, a smiling wom
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 ack top and a silver necklace with a small pendant. The background is blu
 rred\, featuring an elegant architectural setting with warm tones
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
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X-BEDEWORK-IMAGE:/public/Images/Emma Chory canva photo_20250207084014PM.pn
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X-BEDEWORK-THUMB-IMAGE:/public/Images/Emma Chory canva photo_2025020708401
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END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:Artificial intelligence and machine learning have become impor
 tant components of the computational toolbox that can be used to advance 
 chemical research and discovery. Our group has been working on advancing 
 AI/ML as it applies to the broad subfields of synthetic organic chemistry
  (for developing/discovering reactions)\, medicinal chemistry (for develo
 ping/discovering new functional molecules)\, and analytical chemistry (fo
 r elucidating unknown molecular structures using mass spectrometry). A pe
 rvasive theme of our research is the use of domain expertise to inform mo
 deling\, from formulating chemistry challenges as statistical learning pr
 oblems to designing new neural network architectures uniquely suited to c
 hemistry data.
DURATION:PT1H
DTSTAMP:20250214T172115Z
DTSTART;TZID=America/New_York:20250224T120000
LAST-MODIFIED:20250214T172115Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Artificial Intelligence for Molecular Design and Elucidation
UID:CAL-8a000483-92c3adf6-0195-057a0c99-00001502demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
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 incipals/users/agrp_SchoolofMedicine,/principals/users/agrp_SchoolofMedic
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 \,Center for Advanced Genomic Technologies\,Chemistry\,Computer Science\,
 Duke Center for Genomic and Computational Biology (GCB)\,Electrical and C
 omputer Engineering (ECE)\,Precision Genomics Collaboratory\,School of Me
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X-BEDEWORK-SPEAKER:Connor Coley\, PhD
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
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X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
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X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Pictured is Dr. Connor Coley\, PhD\, a man smili
 ng at the camera with short\, light brown hair and glasses\, wearing a li
 ght blue checkered button-up shirt. The background is a modern laboratory
 .
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
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X-BEDEWORK-IMAGE:/public/Images/Connor Coley canva photo_20250214052039PM.
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X-BEDEWORK-THUMB-IMAGE:/public/Images/Connor Coley canva photo_20250214052
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END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:The Leslie lab develops novel computational methods to study c
 ellular biological systems from a global and data-driven perspective. The
 y seek to exploit diverse\, high-throughput functional and genomic data t
 o understand the molecular networks underlying fundamental cellular proce
 sses\, including regulation of transcription\, pre-mRNA processing\, sign
 aling\, and post-transcriptional gene silencing. Today's talk will presen
 t recent machine learning work to exploit single-cell chromatin accessibi
 lity and multiome data to decode gene regulation and cell dynamics.
DURATION:PT1H
DTSTAMP:20250223T202426Z
DTSTART;TZID=America/New_York:20250303T120000
LAST-MODIFIED:20250223T202426Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Decoding Gene Regulation in 3D and in Single Cells
UID:CAL-8a000483-92c3adf6-0195-347b260b-00003323demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
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 iences_ComputerScience,/principals/users/agrp_CenterforGenomicandComputat
 ionalBiology,/principals/users/agrp_AGPM_Collaboratory,/principals/users/
 agrp_SchoolofMedicine,/principals/users/agrp_SchoolofMedicine_UPGG,":Biom
 edical Engineering (BME)\,Biostatistics and Bioinformatics\,Center for Ad
 vanced Genomic Technologies\,Computer Science\,Duke Center for Genomic an
 d Computational Biology (GCB)\,Precision Genomics Collaboratory\,School o
 f Medicine (SOM)\,University Program in Genetics &amp\;amp\; Genomics (UP
 GG)
X-BEDEWORK-SPEAKER:Christina Leslie\, PhD
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
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X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Pictured is Dr. Christina Leslie\, PhD\, a woman
  smiling warmly at the camera\, with long dark hair and glasses. She is w
 earing a dark-colored blouse with a lighter\, olive-green section near th
 e neckline. The background is blurred\, suggesting an indoor setting with
  natural light.
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Christina Leslie canva photo_2025022308240
 0PM.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Christina Leslie canva photo_2025022
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END:VEVENT
BEGIN:VEVENT

CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=00f1fcdb-0f068baf-010f-068baf83-00000004:None
CREATED:20241002T200240Z
DESCRIPTION:The Department of Chemistry is excited to host Professor Xiaog
 uang Lei (Peking University) for a departmental seminar on Monday\, March
  10\, 2025. To learn more about Prof. Brudvig's research\, please visit: 
 https://www.chem.pku.edu.cn/leigroup/proflei/index.htm hosted by Prof. Qi
 u Wang
DURATION:PT1H
DTSTAMP:20250306T145528Z
DTSTART;TZID=America/New_York:20250310T114000
LAST-MODIFIED:20250306T145528Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Chemistry Seminar
UID:CAL-8a00048d-91324965-0192-4ed3ddfb-00003d8edemobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-SPEAKER:Professor Xiaoguang Lei
X-BEDEWORK-SUBMITTEDBY:bsg25 for Chemistry (agrp_ArtsandSciences_Chemistry
 )
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Technology
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:Digital health is rapidly expanding due to surging healthcare 
 costs\, deteriorating health outcomes\, and the growing prevalence and ac
 cessibility of mobile health and wearable technologies. Recent technologi
 cal advancements make it possible to closely and continuously monitor ind
 ividuals using multiple measurement modalities in real time. We are colle
 cting and integrating such wearables data with clinical information to ga
 in a more precise understanding of health and disease and develop actiona
 ble\, predictive health models for improving cardiometabolic and infectio
 us respiratory disease outcomes. We are simultaneously developing open so
 urce data science and machine learning tools for the digital health commu
 nity\, including the Digital Biomarker Discovery Pipeline (DBDP)\, to fac
 ilitate the use of mobile device data in healthcare.
DURATION:PT1H
DTSTAMP:20250403T161457Z
DTSTART;TZID=America/New_York:20250414T120000
LAST-MODIFIED:20250403T161457Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:The Digital Physiome: Wearables for Disease Detection and Monitori
 ng
UID:CAL-8a000483-92c3adf6-0195-fc6e8b6f-00003c64demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_PrattSc
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 iences_ComputerScience,/principals/users/agrp_SOM_ClinDep_Surgery,/princi
 pals/users/agrp_CenterforGenomicandComputationalBiology,/principals/users
 /agrp_SchoolofMedicine,/principals/users/agrp_SchoolofMedicine_UPGG,":Bio
 medical Engineering (BME)\,Biostatistics and Bioinformatics\,Center for A
 dvanced Genomic Technologies\,Computer Science\,Department of Surgery\,Du
 ke Center for Genomic and Computational Biology (GCB)\,School of Medicine
  (SOM)\,University Program in Genetics &amp\;amp\; Genomics (UPGG)
X-BEDEWORK-SPEAKER:Jessilyn Dunn\, PhD
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Pictured is Dr. Jessilyn Dunn\, a woman with lig
 ht skin\, long brown hair\, and black-framed glasses. She is smiling and 
 wearing a navy blue blazer over a white blouse. The background features a
  computer screen displaying colorful graph lines and data charts.
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-LOCATION:Zoom
X-BEDEWORK-IMAGE:/public/Images/Jessilyn Dunn canva photo_20250403041417PM
 .png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Jessilyn Dunn canva photo_2025040304
 1417PM-thumb.png
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Technology:/user/public-user
 /Topics/Technology
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Natural Sciences
CATEGORIES:Utilities
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=00f1fcdb-0f068baf-010f-068baf83-00000004:None
CREATED:20250414T155843Z
DESCRIPTION:The Department of Chemistry is thrilled to host Prof. Ron Naam
 an (Weizmann Institute of Science) on Thursday\, May 8\, 2025 for a depar
 tmental seminar. \n\n"Chirality and the electron spin- A miraculous match
 "\n\nSpin based properties\, applications\, and devices are commonly rela
 ted to magnetic effects and to magnetic materials. However\, we establish
 ed that chiral organic molecules or chiral inorganic materials can act as
  spin filters for photoelectrons transmission\, in electron transfer\, an
 d in electron transport. The effect\, termed Chiral Induced Spin Selectiv
 ity (CISS)\, has interesting implications for the production of new types
  of spintronics devices  and on the importance of chiral molecules in bio
 logical systems. The basic effect\, and its mechanism\, applications and 
 implications\, will be presented.\n\nTo learn more about Prof. Naaman\, p
 lease visit: https://www.weizmann.ac.il/chembiophys/naaman/home\n\nSemina
 r hosted by Profs. David Beratan and Michael Therien
DURATION:PT1H
DTSTAMP:20250414T155843Z
DTSTART;TZID=America/New_York:20250508T133000
LAST-MODIFIED:20250414T155843Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Chemistry Seminar Presented by Prof. Ron Naaman\, "Chirality and t
 he electron spin- A miraculous match"
UID:CAL-8a000483-92c3adf6-0196-35064015-00001168demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-SPEAKER:Prof. Ron Naaman (Weizmann Institute of Science)
X-BEDEWORK-DUKE-SERIES:Chemistry Seminar Series
X-BEDEWORK-STUDENT-CONTACT;X-BEDEWORK-PARAM-EMAIL=chem-office@duke.edu:Dep
 artment of Chemistry
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:41
X-BEDEWORK-IMAGE-X2:1200
X-BEDEWORK-IMAGE-Y2:841
X-BEDEWORK-IMAGE-CROP-WIDTH:1200
X-BEDEWORK-IMAGE-CROP-HEIGHT:800
X-BEDEWORK-IMAGE-ALT-TEXT:Researcher in dark framed rectangular glasses\, 
 light blue collared button up shirt stands in front of library shelving.
X-BEDEWORK-SUBMITTEDBY:cconti for Chemistry (agrp_ArtsandSciences_Chemistr
 y)
X-BEDEWORK-IMAGE:/public/Images/Naaman_20250414035844PM.jpg
X-BEDEWORK-THUMB-IMAGE:/public/Images/Naaman_20250414035844PM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Teaching & Classroom Learning
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Conference/Symposium
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=00f1fcdb-0f068baf-010f-068baf83-00000004:None
CREATED:20250429T202042Z
DESCRIPTION:The NC CER group brings together chemistry education researche
 rs as well as scholars of teaching and learning to share research and pra
 ctices across the state.\n\nThe annual meeting will be held on Friday\, J
 une 6 in French Science Room 4233. All are invited to join\, no registrat
 ion required.\n\nLearn more about Facilitators\, Presenters\, and agenda 
 for the day here: https://duke.box.com/s/p7xjwx60zzpbbzcfocysvqok6nwuhb4s
 
DURATION:PT7H
DTSTAMP:20250429T202301Z
DTSTART;TZID=America/New_York:20250606T100000
LAST-MODIFIED:20250429T202301Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:NC Chemistry Educators and Researchers  Meeting
UID:CAL-8a000483-92c3adf6-0196-83357ea7-00001c30demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Conference_Symposium:/user/p
 ublic-user/Lectures_Conferences/Conference_Symposium
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-STUDENT-CONTACT;X-BEDEWORK-PARAM-EMAIL=charlie.cox@duke.edu:Pro
 f. Charlie Cox
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME="Teaching &amp; Classroom Le
 arning":/user/public-user/Topics/Teaching Classroom Learning
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:73
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X-BEDEWORK-IMAGE-CROP-WIDTH:530
X-BEDEWORK-IMAGE-CROP-HEIGHT:353.3333333333333
X-BEDEWORK-IMAGE-ALT-TEXT:NCCER Logo
X-BEDEWORK-SUBMITTEDBY:cconti for Chemistry (agrp_ArtsandSciences_Chemistr
 y)
X-BEDEWORK-IMAGE:/public/Images/NCCER2_20250429082042PM.jpg
X-BEDEWORK-THUMB-IMAGE:/public/Images/NCCER2_20250429082042PM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=00f1fcdb-0f068baf-010f-068baf83-00000004:None
CREATED:20250616T152418Z
DESCRIPTION:Transition metal catalysis has emerged as an invaluable tool f
 or the development of novel reaction systems. Transition metal catalyzed 
 amination strategies are of the utmost importance due to the ubiquity of 
 nitrogen in bioactive compounds of interest\, ligands\, and catalysts. Gi
 ven the high degree of molecular complexity within the sought-after nitro
 gen-containing compounds\, reactions that are able to install multiple fu
 nctionalities in fewer steps are more useful. To this end\, difunctionali
 zation reactions have been researched using transition metal catalysis. T
 he majority of the works already reported on transition metal catalyzed a
 minofunctionalization rely on alkenes as substrates. However\, alkenes ar
 e generally limited to accessing 1\,2-addition products.\nContrary to sim
 ple alkenes\, 1\,3-dienes offer access to a wide variety of isomeric prod
 ucts to deliver a range of aminated motifs based on regio-\, site-\, and 
 geometric selectivity. Despite this\, the subject of 1\,3-diene 1\,4-amin
 ofunctionalizaiton remains underdeveloped and demands further study.\nBas
 ed on this gap in the field\, a copper-catalyzed 1\,4-aminohydroxylation 
 reaction has been developed using O-benzoylhydroxylamines as an electroph
 ilic source of aliphatic amines. The transformation delivers exclusively 
 1\,4-aminohydroxylated products by means of a carbonyl-assisted migration
  pathway\, as confirmed by various mechanistic experiments. The reaction 
 system is amenable to a wide variety of carbonyl-containing 1\,3-diene su
 bstrates and has been successfully expanded to deliver exclusive 1\,4-ami
 nothiolated products from thioamide-containing 1\,3-dienes.\nCyclopropane
 s represent another class of difunctionalization substrate that remains u
 nderdeveloped. The difunctionalization of cyclopropanes by ring-opening r
 eactions serves as an access point to 1\,3-functionalized motifs\, a subs
 titution pattern inaccessible by alkene or diene functionalization. Utili
 zing the unique reactivity of cyclopropanes for ring-opening difunctional
 ization\, an enantioselective copper-catalyzed 1\,3-aminoalkynylation of 
 non-activated aryl cyclopropanes has been established.
DURATION:PT1H
DTSTAMP:20250701T125624Z
DTSTART;TZID=America/New_York:20250710T130000
LAST-MODIFIED:20250701T125624Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Defense: Noah Watkins- Catalytic selective aminofunctionalzation o
 f 1\, 3 dienes & aryl cyclopropanes enabled by copper catalysis
UID:CAL-8a00f286-97700737-0197-79575f20-0000106cdemobedework@mysite.edu
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
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X-BEDEWORK-IMAGE-ALT-TEXT:NW
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 )
X-BEDEWORK-IMAGE:/public/Images/Noah W. _20250630072416PM.jpg
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END:VEVENT
BEGIN:VEVENT

CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Research
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=00f1fcdb-0f068baf-010f-068baf83-00000004:None
CREATED:20250716T174810Z
DESCRIPTION:I. Kinetic Analysis of Benzylidene Transfer from Gold(I) Carbe
 noids\nII. Kinetic Analysis of Protodeauration of β-Styrenyl Gold Complex
 es\nIII. Palladium (II) Catalyzed Homobenzylic Diazirine Activation\n\nI.
  Aliphatic and aromatic alkenes react rapidly and efficiently with the go
 ld sulfonium benzylide complex [(P)AuCHPh(SPh2)]+{B [3\,5-CF3C6H3]4− [P= 
 P (t-Bu)2o-biphenyl\;1] at room temperature via the cationic two-coordina
 te gold benzylidene complex [(P)AuCHPh]+(1.I) to form phenyclyclopropanes
 . The reactivity of p-substituted vinyl arenes toward 1.I decreased with 
 the decreasing electron donor ability of the vinyl arene and the reactivi
 ty of aliphatic alkenes toward 1.I depended strongly on the number of alk
 yl groups attached to the more substituted alkene terminus.. Benzylidene 
 transfer to vinyl arenes led to predominant formation of cis-cyclopropane
 s. All our experimental observations were consistent with a concerted\, a
 synchronous\, electrophilic benzylidene transfer mechanism.\n\nII. Treatm
 ent of gold β-styrenyl complexes (E)-(PPh3)AuC(H)═C(H)(4-C6H4X) with exce
 ss acetic acid in CD2Cl2 containing PPh3 at 4 °C led to quantitative prot
 odeauration to form the corresponding vinyl arene as the exclusive organi
 c product. Kinetic analysis of the protodeauration under these conditions
  established the rate law for the protodeauration of : rate =k[β-styrenyl
  complex][AcOH]mon\,\, and established the superior correlation of log(ko
 bs) with the Hammett σ parameter (ρ = −1.26\;R2> 0.99) These and addition
 al observations are consistent with a mechanism for the preponderation of
  complexes involving transfer of proton from monomeric acetic acid to the
  Au-C bond with concerted C-H bond formation/Au-C(σ) bond cleavage.\n\nII
 I. Treatment of homobenzylic diazirines 3-(4-chlorobenzyly)-3H-diazirine 
 and 3-benzyl-3H diazirine with a catalytic amount of PdCl2(PhCN)2 (15 mM 
 Pd) at 25 °C led to consumption of the diazirine and yielding correspondi
 ng vinyl arenes as the exclusive organic product. Kinetic analysis of thi
 s palladium catalyzed diazirine activation under these conditions establi
 shed the rate law rate = k[diazirine][Pd]. The elimination also proceeded
  using {PdCl2[π(p-chlorostyrene)}2 as a catalyst in the same conditions. 
 The mechanism is proposed to proceed through an oxidative addition\, foll
 owed by diazometallacyclobutane formation\, then expulsion of nitrogen pr
 oduces the palladium carbene\, which then proceeds through a facile 1\,2-
 elimination.
DURATION:PT1H
DTSTAMP:20250716T195736Z
DTSTART;TZID=America/New_York:20250717T100000
LAST-MODIFIED:20250716T195736Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Chemistry Defense: Mitch Rivers: I. Kinetic Analysis of Benzyliden
 e Transfer from Gold(I) Carbenoids  II. Kinetic Analysis of Protodeaurati
 on of β-Styrenyl Gold Complexes  III. Palladium (II) Catalyzed Homobenzyl
 ic Diazirine Activation
UID:CAL-8a00ec8b-979413b9-0198-1459ddad-000008eedemobedework@mysite.edu
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 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-STUDENT-CONTACT;X-BEDEWORK-PARAM-EMAIL=chem-office@duke.edu:Che
 mistry Admin office
X-BEDEWORK-SPEAKER:Mitch Rivers
X-BEDEWORK-IMAGE-X1:713
X-BEDEWORK-IMAGE-Y1:305
X-BEDEWORK-IMAGE-X2:1243
X-BEDEWORK-IMAGE-Y2:658.3333333333333
X-BEDEWORK-IMAGE-CROP-WIDTH:530
X-BEDEWORK-IMAGE-CROP-HEIGHT:353.33333333333326
X-BEDEWORK-IMAGE-ALT-TEXT:mitch rivers
X-BEDEWORK-SUBMITTEDBY:lao26 for Chemistry (agrp_ArtsandSciences_Chemistry
 )
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X-BEDEWORK-THUMB-IMAGE:/public/Images/Admin Office Slides _20250716054810P
 M-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Technology
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:David Rasmussen leads the Phylodynamics Research Group at NC S
 tate\, which focuses on developing new computational and statistical meth
 ods for genomic epidemiology\, population genomics and phylogenetics. Muc
 h of our research focuses on developing "phylodynamic" methods to better 
 understand the evolution of microbial pathogens by combining population d
 ynamic modeling with phylogenetic methods. We have applied these approach
 es to RNA viruses and bacteria to explore the genomic determinants of pat
 hogen fitness in real world environments and to identify potential fitnes
 s trade-offs between alternate environments. Recent work has also focused
  on optimizing sampling designs for demographic inference from population
  genomic data. Framing genomic sampling as a sequential decision making p
 roblem (i.e. a Markov decision process)\, allows us to maximize the infor
 mation gained from genomic data about a population's history using classi
 c dynamic programming and modern reinforcement learning methods.
DURATION:PT1H
DTSTAMP:20260202T003952Z
DTSTART;TZID=America/New_York:20260202T120000
LAST-MODIFIED:20260202T003952Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CANCELLED
SUMMARY:CANCELED: Optimizing Genomic Sampling to Learn the Evolutionary Hi
 story of Pathogen Populations
UID:CAL-8a00eca5-9af98aae-019b-f2320fad-00006e0fdemobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Technology:/user/public-user
 /Topics/Technology
X-BEDEWORK-LOCATION:FFSC 4233
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_Artsand
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 enterforGenomicandComputationalBiology,/principals/users/agrp_SchoolofMed
 icine_MolecularGenetics,/principals/users/agrp_SchoolofMedicine_Neurobiol
 ogy,/principals/users/agrp_SchoolofMedicine_CMB,/principals/users/agrp_Sc
 hoolofMedicine,/principals/users/agrp_SchoolofMedicine_UPGG,":Biology\,Bi
 ostatistics and Bioinformatics\,Center for Advanced Genomic Technologies\
 ,Duke Center for Genomic and Computational Biology (GCB)\,Molecular Genet
 ics and Microbiology (MGM)\,Neurobiology\,Program in Cell and Molecular B
 iology\,School of Medicine (SOM)\,University Program in Genetics &amp\;am
 p\;amp\;amp\;amp\;amp\;amp\;amp\;amp\; Genomics (UPGG)
X-BEDEWORK-SPEAKER:David Rasmussen\, PhD
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
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X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
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X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:David Rasmussen
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/David Rasmussen canva photo_20260124104845
 PM.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/David Rasmussen canva photo_20260124
 104845PM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Technology
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:The Johri lab is interested in better characterizing the shape
  of the distribution of fitness effects of new mutations in organisms and
  on understanding how selection on functionally important regions affects
  genome-wide patterns of variation. Population genomic inference currentl
 y does not account for the effects of selection across the genome\, which
  is especially problematic in species with compact genomes (i.e.\, those 
 with a high density of protein-coding and regulatory regions) where natur
 al selection is pervasive. We develop statistical and computational metho
 ds that simultaneously account for the effects of selection jointly with 
 other evolutionary processes to make accurate evolutionary inferences (su
 ch as historical changes in population size) using sequence variation fro
 m natural populations. As most pathogenic species tend to have highly com
 pact genomes and experience strong bouts of selection and drastic repeate
 d bottlenecks\, our methodological advances and recent theoretical effort
 s will be important to uncovering their population and selective history.
 
DURATION:PT1H
DTSTAMP:20260209T020656Z
DTSTART;TZID=America/New_York:20260216T120000
LAST-MODIFIED:20260209T020656Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Jointly Modeling the Effects of Evolutionary Processes on Genomic 
 Variation
UID:CAL-8a00eca5-9af98aae-019c-40222334-00005922demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Technology:/user/public-user
 /Topics/Technology
X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_Artsand
 Sciences_Biology,/principals/users/agrp_SchoolofMedicine_Biostatisticsand
 Bioinformatics,/principals/users/agrp_Pratt_CAGT,/principals/users/agrp_C
 enterforGenomicandComputationalBiology,/principals/users/agrp_SchoolofMed
 icine_MolecularGenetics,/principals/users/agrp_SchoolofMedicine_Neurobiol
 ogy,/principals/users/agrp_SchoolofMedicine_CMB,/principals/users/agrp_Sc
 hoolofMedicine,/principals/users/agrp_SchoolofMedicine_UPGG,":Biology\,Bi
 ostatistics and Bioinformatics\,Center for Advanced Genomic Technologies\
 ,Duke Center for Genomic and Computational Biology (GCB)\,Molecular Genet
 ics and Microbiology (MGM)\,Neurobiology\,Program in Cell and Molecular B
 iology\,School of Medicine (SOM)\,University Program in Genetics &amp\;am
 p\;amp\;amp\;amp\;amp\;amp\;amp\; Genomics (UPGG)
X-BEDEWORK-SPEAKER:Parul Johri\, PhD
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:529.5
X-BEDEWORK-IMAGE-Y2:353
X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Parul Johri
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Parul Johri canva photo_20260209020144AM.j
 pg
X-BEDEWORK-THUMB-IMAGE:/public/Images/Parul Johri canva photo_202602090201
 44AM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
CATEGORIES:Natural Sciences
CATEGORIES:Lectures/Conferences
CATEGORIES:Utilities
CATEGORIES:Lecture/Talk
CATEGORIES:Panel/Seminar/Colloquium
CATEGORIES:Research
CATEGORIES:Technology
CATEGORIES:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:Research in the Velmeshev lab uses single-cell genomics\, spat
 ial transcriptomic and transsynaptic viral tracing applied to human brain
  tissue samples\, cerebral organoids\, and rodent models to understand ce
 ll type-specific mechanisms of brain development and neurodevelopmental d
 isorders such as autism. Velmeshev lab also develops bioinformatics tools
  for analyzing single-cell and spatial transcriptomics data.
DURATION:PT1H
DTSTAMP:20260225T153014Z
DTSTART;TZID=America/New_York:20260302T120000
LAST-MODIFIED:20260225T153014Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Dissecting Developing and Mature Neuronal Circuit Organization Usi
 ng Barcoded Transsynaptic Viral Tracing\, Spatial Transcriptomics and Bio
 informatics
UID:CAL-8a003294-9c52b03d-019c-956be646-000004dcdemobedework@mysite.edu
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 ties/Main
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
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X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Technology:/user/public-user
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X-BEDEWORK-CS;X-BEDEWORK-PARAM-DESCRIPTION="/principals/users/agrp_Artsand
 Sciences_Biology,/principals/users/agrp_PrattSchool_BME,/principals/users
 /agrp_SchoolofMedicine_BiostatisticsandBioinformatics,/principals/users/a
 grp_Pratt_CAGT,/principals/users/agrp_CenterforGenomicandComputationalBio
 logy,/principals/users/agrp_SchoolofMedicine_MolecularGenetics,/principal
 s/users/agrp_SchoolofMedicine_Neurobiology,/principals/users/agrp_Schoolo
 fMedicine_CMB,/principals/users/agrp_SchoolofMedicine,/principals/users/a
 grp_SchoolofMedicine_UPGG,":Biology\,Biomedical Engineering (BME)\,Biosta
 tistics and Bioinformatics\,Center for Advanced Genomic Technologies\,Duk
 e Center for Genomic and Computational Biology (GCB)\,Molecular Genetics 
 and Microbiology (MGM)\,Neurobiology\,Program in Cell and Molecular Biolo
 gy\,School of Medicine (SOM)\,University Program in Genetics &amp\; Genom
 ics (UPGG)
X-BEDEWORK-SPEAKER:Dmitry Velmeshev\, PhD
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
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X-BEDEWORK-IMAGE-X2:529.5
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X-BEDEWORK-IMAGE-CROP-WIDTH:529.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:353
X-BEDEWORK-IMAGE-ALT-TEXT:Dmitry Velmeshev
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Dmitry Velmeshev canva photo_2026022503300
 2PM.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Dmitry Velmeshev canva photo_2026022
 5033002PM-thumb.png
END:VEVENT
END:VCALENDAR

