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DTSTART:19450814T190000
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BEGIN:VEVENT

CATEGORIES:Medicine
CATEGORIES:Engineering
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:20230210T113930Z
DESCRIPTION:Dr. Jason H. Yang is an Assistant Professor and Chancellor Sch
 olar in the Rutgers New Jersey Medical School Center for Emerging Pathoge
 ns and Department of Microbiology\, Biochemistry & Molecular Genetics. He
  leads a systems and synthetic biology research program focused on basic 
 and translational research into antimicrobial resistance\, tuberculosis\,
  and immune cell therapies. Projects in the Yang lab combine the use of m
 athematical models\, machine learning\, and bioinformatic approaches with
  quantitative and high-throughput experimental techniques to study and en
 gineer the processes underlying microbial and mammalian cell fates.
DURATION:PT1H
DTSTAMP:20230210T115535Z
DTSTART;TZID=America/New_York:20230327T120000
LAST-MODIFIED:20230210T115535Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Systems Biology Insights Into Antimicrobial Resistance Evolution a
 nd Physiology
UID:CAL-8a0290b4-860465b2-0186-3b1f93a3-0000381ademobedework@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=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=Research:/user/public-user/T
 opics/Research
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:Jason Yang
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:-0.3333333333333144
X-BEDEWORK-IMAGE-X2:530
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X-BEDEWORK-IMAGE-CROP-HEIGHT:353.3333333333333
X-BEDEWORK-IMAGE-ALT-TEXT:Jason Yang\, PhD\, Assistant Professor and Chanc
 ellor Scholar in the Rutgers New Jersey Medical School Center
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Jason Yang_20230210115535AM.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Jason Yang_20230210115535AM-thumb.pn
 g
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:20230228T143412Z
DESCRIPTION:RNA binding proteins (RBPs) are key regulators of gene express
 ion. I will describe a new resource\, the RBPzoo\, which contains RNA mot
 ifs derived from in vitro selection data for 381 eukaryotic RBPs. I will 
 also introduce a new machine learning algorithm\, Joint Protein-Ligand Em
 bedding (JPLE)\, which we trained on RBPzoo to learn a mapping from an RB
 P's sequence to its RNA motif. We used JPLE to assign RNA motifs and the 
 specificity-determining residues to protein sequences for nearly 30\,000 
 RBPs from 690 eukaryotes. To illustrate the power of this resource\, we i
 dentify 12 Arabidopsis thaliana mRNA-stability-affecting RBPs based only 
 on their amino acid sequence and tissue-specific RNA-seq for A. thaliana.
  We also reconstruct the evolution of >2\,500 groups of RBP motifs\, find
 ing that 19 motifs representing core RNA processing functions are deeply 
 conserved between plants and metazoa. Finally\, we identify three phases 
 of rapid motif expansion: one corresponding with two whole-genome-duplica
 tions in the vertebrate lineage and two recent expansions in the flowerin
 g plants and nematode lineages.
DURATION:PT1H
DTSTAMP:20230329T122648Z
DTSTART;TZID=America/New_York:20230403T120000
LAST-MODIFIED:20230329T122648Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:RBPzoo: The Motifs\, Binding Interface and Evolution History of 30
 \,000 Eukaryotic RNA-binding Proteins (RBPs)
UID:CAL-8a0290b4-860465b2-0186-9871ff17-000051a7demobedework@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=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
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-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-SPEAKER:Quaid Morris
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:91
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:1711
X-BEDEWORK-IMAGE-Y2:1080
X-BEDEWORK-IMAGE-CROP-WIDTH:1620
X-BEDEWORK-IMAGE-CROP-HEIGHT:1080
X-BEDEWORK-IMAGE-ALT-TEXT:Quaid Morris\, PhD\, Program in Computational an
 d Systems Biology
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Quaid Morris canva photo_20230315060516PM.
 png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Quaid Morris canva photo_20230315060
 516PM-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:20230316T143327Z
DESCRIPTION:Tumors are no longer thought of as clonal expansions driven so
 lely by genetic events. In reality\, cancers are made up of multiple tumo
 r cell states that are defined by transcriptional and epigenetic features
  superimposed on a mutational background. By integrating multiple types o
 f single cell profiling (transcriptome\, chromatin accessibility\, histon
 e modification specific profiling) we seek to better understand how cell 
 states change over time and under therapeutic pressure. In addition\, we 
 attempt to model tumor evolutionary responses using patient derived model
  systems (specifically xenografts and tumor slice cultures) that more fai
 thfully recapitulate the cell state heterogeneity seen in patients. Ultim
 ately we hope to derive insights from single cell profiling that will lea
 d to cell state directed therapeutic approaches to GBM and other malignan
 cies.
DURATION:PT1H
DTSTAMP:20230317T182622Z
DTSTART;TZID=America/New_York:20230410T120000
LAST-MODIFIED:20230317T182622Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Multiomic Characterization of Cell State Heterogeneity in Human Br
 ain Tumors
UID:CAL-8a0290b4-860465b2-0186-ead7100d-00003e99demobedework@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=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
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:Anoop Patel
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. Anoop Patel\, Department of Neurosurgery
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Anoop Patel canva photo_20230316030531PM.p
 ng
X-BEDEWORK-THUMB-IMAGE:/public/Images/Anoop Patel canva photo_202303160305
 31PM-thumb.png
END:VEVENT
BEGIN:VEVENT

CATEGORIES:Medicine
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:20230213T001036Z
DESCRIPTION:The Gibbons lab sits at the intersection of systems biology an
 d microbial ecology. We develop computational and wet-lab tools for explo
 ring and manipulating host-microbe ecosystems. Currently\, we are interes
 ted in designing a mechanistic modeling platform that enables precision n
 utrition and personalized healthcare interventions that leverage the meta
 bolic output of the human gut microbiome.
DURATION:PT1H
DTSTAMP:20230213T001125Z
DTSTART;TZID=America/New_York:20230417T120000
LAST-MODIFIED:20230213T001125Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Community-Scale Metabolic Menables Precision Microbiome Engineerin
 g
UID:CAL-8a0290b4-860465b2-0186-481bf6a5-000003e4demobedework@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=Panel_Seminar_Colloquium:/us
 er/public-user/Lectures_Conferences/Panel_Seminar_Colloquium
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
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:Sean Gibbons
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:Sean Gibbons\, Institute for Systems Biology
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Sean Gibbons canva photo_20230213121037AM.
 png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Sean Gibbons canva photo_20230213121
 037AM-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:20230515T152526Z
DESCRIPTION:Many plant pathogens are microbial and can evolve much faster 
 than plants. How can plants stay in this race of evolution against pathog
 ens with lopsided disadvantage? An answer is that plants hide and change 
 the goal of the race instead of fairly competing in the race. I will disc
 uss two of the mechanisms with which plants hide and change the goal: res
 ilience of the immune signaling network and coevolution of homologous imm
 une regulators. I will also discuss how plants limit the battlegrounds us
 ing these mechanisms.
DURATION:PT1H
DTSTAMP:20230515T152526Z
DTSTART;TZID=America/New_York:20230518T133000
LAST-MODIFIED:20230515T152526Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Biology Seminar | Professor Fumiaki Katagiri\, University of Minne
 sota | How can plants stay in this world while their pathogens can evolve
  much faster?
UID:CAL-8a008e08-881ff5df-0188-2004375c-000000bfdemobedework@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=mindy.sponsel@duke.edu:M
 indy Sponsel
X-BEDEWORK-SUBMITTEDBY:bbooher for Biology (agrp_ArtsandSciences_Biology)
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:20230813T193533Z
DESCRIPTION:Dr. Rohit Singh is an Assistant Professor in the Departments o
 f Biostatistics & Bioinformatics and Cell Biology at Duke University. Dru
 g discoveries have been instrumental in improving global health over the 
 last century\, but the median drug now takes about 10 years to bring to m
 arket and costs over a billion dollars to develop. My work aims to expedi
 te the development of precise diagnostics and therapeutics by applying ma
 chine learning. In this talk\, I will outline two recent research directi
 ons. In the first part\, we use single-cell multiomics to discover regula
 tory mechanisms governing the interaction between the epigenome\, transcr
 iption factors\, and target genes. This approach relies on methodological
  innovation\, developing new Granger causal inference techniques to capit
 alize on the "parallax" between simultaneous but separate measures of cel
 l state. In the second part\, I will introduce the application of large l
 anguage models to model protein interaction and function. These protein l
 anguage models enable powerful new approaches to predicting and understan
 ding protein-protein and protein-drug interactions. I will conclude with 
 a prospective look at how similar methods may help answer foundational qu
 estions in both basic and translational science.
DURATION:PT1H
DTSTAMP:20230813T193720Z
DTSTART;TZID=America/New_York:20230828T120000
LAST-MODIFIED:20230813T193720Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Machine Learning for Precise Diagnostics and Therapeutics
UID:CAL-8a028ad1-899cba17-0189-f0658c19-00002192demobedework@mysite.edu
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Main:/user/public-user/Utili
 ties/Main
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=Medicine:/user/public-user/T
 opics/Medicine
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Technology:/user/public-user
 /Topics/Technology
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Engineering:/user/public-use
 r/Topics/Engineering
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
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:Rohit Singh\, PhD
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:0
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X-BEDEWORK-IMAGE-CROP-HEIGHT:353.3333333333333
X-BEDEWORK-IMAGE-ALT-TEXT:Rohit Singh\, PhD\, Assistant Professor in the D
 epartments of Biostatistics &amp\;amp\; Bioinformatics and Cell Biology a
 t Duke University
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Rohit_cropped resized_20230813073721PM.jpg
 
X-BEDEWORK-THUMB-IMAGE:/public/Images/Rohit_cropped resized_20230813073721
 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:Dr. Carter is an Associate Professor in the Department of Medi
 cine in the Division of Genomics and Precision Medicine at UCSD. The Cart
 er Lab develops and applies computational approaches to aid the interpret
 ation of genetic variation and to advance precision cancer medicine. A ma
 jor focus of the lab is on joint analysis of tumor and inherited genomes 
 to uncover the role of genetic background in shaping cancer risk\, somati
 c tumor evolution and therapeutic response. Her recent work investigates 
 how the inherited immune system affects tumor genome evolution and the ch
 aracteristics of the tumor immune microenvironment to identify opportunit
 ies and barriers for immunotherapy.
DURATION:PT1H
DTSTAMP:20230805T023014Z
DTSTART;TZID=America/New_York:20230911T120000
LAST-MODIFIED:20230805T023014Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Common Variants Influence Immunotherapy Response
UID:CAL-8a028ad1-899cba17-0189-c387f69f-00003ed7demobedework@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:Hannah Carter
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:24
X-BEDEWORK-IMAGE-Y1:70
X-BEDEWORK-IMAGE-X2:733
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X-BEDEWORK-IMAGE-CROP-WIDTH:709
X-BEDEWORK-IMAGE-CROP-HEIGHT:472.66666666666674
X-BEDEWORK-IMAGE-ALT-TEXT:Hannah Carter\, associate professor\, University
  of California San Diego
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Carter_2022_20230805023014AM.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Carter_2022_20230805023014AM-thumb.p
 ng
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:Dr. Evrony is an Assistant Professor at the New York Universit
 y School of Medicine. Evrony lab's mission is to develop foundational new
  technologies for neuroscience and human genetics that will advance our u
 nderstanding of diseases of the brain. We also aim to accelerate the impl
 ementation of genomics in clinical medicine\, especially for children wit
 h rare undiagnosed diseases.
DURATION:PT1H
DTSTAMP:20230907T122610Z
DTSTART;TZID=America/New_York:20230918T120000
LAST-MODIFIED:20230907T122610Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:High-Fidelity DNA Sequencing of the Single-Strand Origins of Mutat
 ions
UID:CAL-8a02906b-8a0a73d8-018a-6f994630-000069c7demobedework@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:Gilad Evrony
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
X-BEDEWORK-IMAGE-X1:1
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:1024
X-BEDEWORK-IMAGE-Y2:682
X-BEDEWORK-IMAGE-CROP-WIDTH:1023
X-BEDEWORK-IMAGE-CROP-HEIGHT:682
X-BEDEWORK-IMAGE-ALT-TEXT:Gilad Evrony\, PhD\, Assistant Professor\, New Y
 ork University School of Medicine
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Gilad-Evrony_portrait-resized_202309071223
 49PM.jpg
X-BEDEWORK-THUMB-IMAGE:/public/Images/Gilad-Evrony_portrait-resized_202309
 07122349PM-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:Jeffrey J. Headd\, PhD is Vice President\, Commercial Data Sci
 ence\, at the Janssen Pharmaceutical Companies of Johnson & Johnson. He l
 eads both the Janssen NA Business Technology Commercial Data Science Chap
 ter and Commercial Data & Insights Product Group. Jeff partners with comm
 ercial leadership across business functions to identify and tackle critic
 al challenges with novel data-driven solutions. His multidisciplinary tea
 m applies expertise in artificial intelligence\, explainable machine lear
 ning\, data integration\, and other modern analytical methods to address 
 these challenges and generate measurable business value.
DURATION:PT1H
DTSTAMP:20230908T204914Z
DTSTART;TZID=America/New_York:20230925T120000
LAST-MODIFIED:20230908T204914Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Driving Impact in Healthcare through Data Science at Scale
UID:CAL-8a02906b-8a0a73d8-018a-768652d5-000076b4demobedework@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:Jeff Headd
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:Jeffrey J. Headd\, PhD is Vice President\, Comme
 rcial Data Science\, at the Janssen Pharmaceutical Companies of Johnson &
 amp\;amp\;amp\;amp\; Johnson
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Jeff Headd canva photo_20230908084835PM.pn
 g
X-BEDEWORK-THUMB-IMAGE:/public/Images/Jeff Headd canva photo_2023090808483
 5PM-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:Dr. Khasraw's research focus is to develop innovative clinical
  trials using immune and targeted therapies and partner biomarkers\, main
 ly in central nervous system tumors\, but I have also published findings 
 across multiple domains and in a diverse range of rare and underserved ca
 ncers. My research is at an interface between clinical trial design\, dat
 a science and translational research take discoveries from the bench to t
 he bedside and back to the bench.
DURATION:PT1H
DTSTAMP:20230908T214837Z
DTSTART;TZID=America/New_York:20231002T120000
LAST-MODIFIED:20230908T214837Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Longitudinal Bioinformatics Analysis to Correct the Drug Developme
 nt Paradigm in Oncology
UID:CAL-8a02906b-8a0a73d8-018a-76c06581-00007a54demobedework@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:Dr. Mustafa Khasraw
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:Mustafa Khasraw\, MD\, Professor of Medicine\, M
 edical Oncology\, and Neuro-Oncology Deputy Director\, Duke Center for Ca
 ncer Immunotherapy
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Mustafa Khasraw canva photo_20230908094720
 PM.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Mustafa Khasraw canva photo_20230908
 094720PM-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:Dr. Bayraktar uses single cell and spatial genomics technologi
 es to characterize human brain cellular diversity in health and disease. 
 During his training\, Omer discovered neural stem cell patterning mechani
 sms and astrocyte layer diversity in the cerebral cortex. His team has de
 veloped the cell2location computational tool to map fine cell types in sp
 atial transcriptomics. Currently\, Bayraktar lab is focused on studying t
 he molecular\, cellular and spatial organization of glioblastoma (GBM)\, 
 where we use single cell and spatial genomics to identify cell-intrinsic 
 and tumor microenvironment derived cures regulating malignancy.
DURATION:PT1H
DTSTAMP:20230929T213252Z
DTSTART;TZID=America/New_York:20231009T120000
LAST-MODIFIED:20230929T213252Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Mapping the Rules of Glioblastoma using Single Cell and Spatial Ge
 nomics
UID:CAL-8a03932d-8a96243a-018a-e2c195b5-00005669demobedework@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:Omer Bayraktar
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:Omer Bayraktar\, PhD\, Group Leader\, Cellular G
 enetics Programme\, Wellcome Sanger Institute
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Omer Bayraktar_20230929090411PM.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Omer Bayraktar_20230929090411PM-thum
 b.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:20230827T185809Z
DESCRIPTION:The Department of Chemistry is excited to host Kelley Young (N
 otre Dame)\nTo learn more about Professor Young\, please visit: https://c
 hemistry.nd.edu/faculty/kelley-young/\n\nGalvin Scholars Program: A Model
  for STEM Retention and Success\nThe University of Notre Dame is a privat
 e university with nearly 9\,000 undergraduates\, and an entering first ye
 ar class of approximately 2\,000 students\, half of which intend to compl
 ete a STEM major. These majors require first year chemistry\, math and ph
 ysics courses taken in the College of Science. Prior to 2018\, attrition 
 from the College of Science during the first year was\nnearly 1 in 3 stud
 ents. The factors most strongly correlated with retention were SAT math s
 cores and the number of AP STEM courses a student had seen in high school
 . Other statistically-significant factors contributing to attrition are l
 ow socioeconomic status (or Pell eligibility)\, First Generation status\,
  and membership in an underrepresented minority group.\n\nTo combat the d
 isproportionate number of students from underserved groups leaving STEM\,
  Notre Dame created the Mary E. Galvin Science and Engineering Scholars P
 rogram\, aimed at increasing retention in STEM by providing support to st
 udents from weaker high school backgrounds. Students are invited to apply
  to the program\, which provides intensive small class sizes for introduc
 tory STEM courses\, additional problem solving courses\, community buildi
 ng\, peer-mentoring\, and academic and professional support. Since its in
 ception in 2018\, the program has supported over 410 students\, including
  the current first year cohort of 80 students. Retention rates for studen
 ts in the Galvin Scholars program are higher than for their peers\, and r
 ecent institutional data has shown that Galvin Scholars outperform their 
 peers with similar academic preparation levels in all STEM courses where 
 support is provided.\n\nThis seminar will discuss development and impleme
 ntation of the Galvin Scholars program as well as the execution and funct
 ion of the academic year and support provided to the students as a model 
 for retention in STEM for underserved students.\n\nHosted by Jim Parise
DURATION:PT1H
DTSTAMP:20231011T161959Z
DTSTART;TZID=America/New_York:20231020T133000
LAST-MODIFIED:20231011T161959Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Chemistry Seminar Presented by Prof. Kelley Young "Galvin Scholars
  Program: A Model for STEM Retention and Success"
UID:CAL-8a02906b-8a0a73d8-018a-385c5439-000069d3demobedework@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:Kelley Young\, Notre Dame
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:0
X-BEDEWORK-IMAGE-X2:1087.5
X-BEDEWORK-IMAGE-Y2:725
X-BEDEWORK-IMAGE-CROP-WIDTH:1087.5
X-BEDEWORK-IMAGE-CROP-HEIGHT:725
X-BEDEWORK-IMAGE-ALT-TEXT:Kelley Young
X-BEDEWORK-SUBMITTEDBY:lao26 for Chemistry (agrp_ArtsandSciences_Chemistry
 )
X-BEDEWORK-IMAGE:/public/Images/kyoungbanner_20230827065809PM.jpg
X-BEDEWORK-THUMB-IMAGE:/public/Images/kyoungbanner_20230827065809PM-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 develops computational methods to understand the genet
 ic and epigenetic bases of gene regulation mainly in human immune cells. 
 We are particularly interested in the analysis and modeling of the 3D gen
 ome organization from high-throughput chromatin conformation capture data
  to understand how changes in this 3D structure affect outcomes such as d
 evelopment\, differentiation\, and disease progression. We also have ongo
 ing interests in systems-level analysis and reconstruction of regulatory 
 networks\, inference of enhancer-promoter contacts\, predictive models of
  gene expression\, analysis of single-cell data\, as well as integrative\
 , comparative\, and high-resolution analysis of chromosomes conformation 
 data such as Hi-C and HiChIP.
DURATION:PT1H
DTSTAMP:20231002T152810Z
DTSTART;TZID=America/New_York:20231023T120000
LAST-MODIFIED:20231002T152810Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Computational Methods for Studying the 3D Organization of the Huma
 n Genome
UID:CAL-8a03932d-8a96243a-018a-f0f68860-00002a06demobedework@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:Ferhat Ay
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:Ferhat Ay\, PhD Associate Professor\, Centers fo
 r Cancer Immunotherapy and Autoimmunity (LJI) &amp\;amp\;amp\;amp\;amp\;a
 mp\;amp\;amp\;amp\;  Department of Pediatrics (UCSD)
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Ferhat Ay canva photo_20231002032452PM.png
 
X-BEDEWORK-THUMB-IMAGE:/public/Images/Ferhat Ay canva photo_20231002032452
 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:Dr. Przytycka's lab focuses on computational methods advancing
  the understanding of biomolecular systems and the emergence of complex p
 henotypes\, including cancer. Her group also develops new computational a
 pproaches to study gene regulation including methods to reconstruct Gene 
 Regulatory Networks\, single cell analysis\, network-based approaches to 
 study mutational processes in cancer and drug response.
DURATION:PT1H
DTSTAMP:20231013T193030Z
DTSTART;TZID=America/New_York:20231030T120000
LAST-MODIFIED:20231013T193030Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Computational Approaches to Delineate Interactions Between Mutagen
 ic Signatures\, Cellular Processes and Environment
UID:CAL-8a0382b5-8b29fde3-018b-2a82b88c-00000ad6demobedework@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:Teresa Przytycka
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:Teresa Przytycka\, PhD\, Senior Investigator at 
 NCBI National Institutes of Health
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Teresa Przytycka canva photo_2023101307303
 0PM.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Teresa Przytycka canva photo_2023101
 3073030PM-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 Trapnell Lab at the University of Washington's Department 
 of Genome Sciences studies how genomes encode the program of vertebrate d
 evelopment and how that program goes awry in disease. We build new tools\
 , technologies\, and software for decoding this program from large-scale 
 single-cell experiments.
DURATION:PT1H
DTSTAMP:20231023T114541Z
DTSTART;TZID=America/New_York:20231106T120000
LAST-MODIFIED:20231023T114541Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Embryo-Scale Reverse Genetics at Single-Cell Resolution
UID:CAL-8a018d0d-8b5366bc-018b-5c5a3a4d-000032bademobedework@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:Cole Trapnell
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:Cole Trapnell\, PhD\, Associate Professor Genome
  Sciences\, University of Washington
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Cole Trapnell canva pic_20231023114458AM.p
 ng
X-BEDEWORK-THUMB-IMAGE:/public/Images/Cole Trapnell canva pic_202310231144
 58AM-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:Biomolecular condensates are membrane-free compartments that s
 patially and temporally organize biochemistry in cells. Nucleic acids are
  frequence drivers and architectural elements in condensates however the 
 molecular grammar that dictates the composition and physical states of co
 ndensates remains mysterious.  To examine how RNA sequence and structure 
 impact the form and function of condensates\, we created an evolutionary 
 algorithm that designs shuffled mRNA sequences which maximize or minimize
  predicted free energies of folding while preserving mass\, known protein
  binding sites\, encoded amino acid sequence\, and nucleotide composition
 . RNAs with minimized free energies of folding contain many stable duplex
 es\, while RNAs with maximized energies have unstable structures and long
  single-stranded regions. Using mass photometry\, we show that RNAs with 
 stable structures are mostly monomeric\, while RNAs with unstable structu
 res can multimerize. When mixed with protein\, these differential RNA-RNA
  interactions affect dense phase compositions. Specifically\, unstable RN
 As form condensates with high RNA and low protein concentrations\, while 
 the converse is true for RNAs with stable structures. Using microbead rhe
 ology\, we observe that unstable RNAs form condensates with long viscoela
 stic relaxation times that increase with condensate age\, indicating elas
 tic properties at many timescales. By contrast\, stable RNAs form less el
 astic condensates with shorter relaxation times that increase to a lesser
  degree with time. We hypothesize that such aging is controlled by the ex
 change of intra- for inter-molecular base pairing among RNAs whose foldin
 g free energies determine the timescale of such exchanges. Thus\, RNA str
 ucture can have multi-scale consequences for biomolecular condensates\, w
 ith impacts on condensate composition and material properties.
DURATION:PT1H
DTSTAMP:20231031T183707Z
DTSTART;TZID=America/New_York:20231113T120000
LAST-MODIFIED:20231031T183707Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Encoding Physical Properties of the Cytosol
UID:CAL-8a018d0d-8b5366bc-018b-87059ba3-000020e5demobedework@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:Amy Gladfelter
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:Amy Gladfelter PhD\, Professor\, Cell Biology Du
 ke University
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Amy Gladfelter canva_20231031063613PM.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Amy Gladfelter canva_20231031063613P
 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:Main
CONTACT;X-BEDEWORK-UID=8a0183a7-83184018-0184-f88b4dd1-00001a24:Franklin\,
  Monica
CREATED:20230805T023014Z
DESCRIPTION:This talk introduces a mathematical theory of developmental bi
 ology\, based on optimal transport. While\, in principle\, organisms are 
 made of molecules whose motions are described by the Schrödinger equation
 \, there are simply too many molecules for this to be useful. Optimal tra
 nsport-a fascinating topic in its own right\, at the intersection of prob
 ability\, statistics and optimization-provides a set of equations that de
 scribe development at the level of cells. Biology has entered a new era o
 f precision measurement and massive datasets. Techniques like single-cell
  RNA sequencing (scRNA-seq) and single-cell ATAC-seq have emerged as powe
 rful tools to profile cell states at unprecedented molecular resolution. 
 One of the most exciting prospects associated with this new trove of data
  is the possibility of studying temporal processes\, such as differentiat
 ion and development. If we could understand the genetic forces that contr
 ol embryonic development\, then we would have a better idea of how cell t
 ypes are stabilized throughout adult life and how they destabilize with a
 ge or in diseases like cancer. This would be within reach if we could ana
 lyze the dynamic changes in gene expression\, as populations develop and 
 subpopulations differentiate. However\, this is not directly possible wit
 h current measurement technologies because they are destructive (e.g. cel
 ls must be lysed to measure expression profiles). Therefore\, we cannot d
 irectly observe the waves of transcriptional patterns that dictate change
 s in cell type.
DURATION:PT1H
DTSTAMP:20231115T144111Z
DTSTART;TZID=America/New_York:20231120T120000
LAST-MODIFIED:20231115T144111Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Towards a Mathematical Theory of Development
UID:CAL-8a018ccf-8b87f80e-018b-d2ff328d-00001cb7demobedework@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:Geoff Schiebinger
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:Geoffrey Schiebinger\, PhD\, Department of Mathe
 matics\, University of British Columbia
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Geoff Schiebinger canva photo_202311151240
 21PM.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Geoff Schiebinger canva photo_202311
 15124021PM-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:20231218T182616Z
DESCRIPTION:"Next-generation precision medicine through covalent reactivit
 y: from click chemistry to 'undruggable' targets"\n\nCovalent chemical re
 activity is a powerful means for the discovery of diverse functional mole
 cules. In this talk\, I will first focus on the next-generation click che
 mistry\, sulfur fluoride exchange (SuFEx). I will demonstrate how the sel
 ectivity\, efficiency\, and fidelity of modular SuFEx reactions accelerat
 e the discovery of therapeutic and diagnostic molecules. I will then high
 light the recent development of in vivo active covalent inhibitors target
 ing K-Ras(G12D)\, the most common activating mutation found in human canc
 er. K-Ras lacks surface topology for reversible small molecule binding\, 
 leading to its notorious characterization as 'undruggable'. I will report
  on a series of compounds that rely on covalent reaction with mutant aspa
 rtic acid for binding and therefore do not affect the wildtype protein (W
 T). I will discuss the potency and selectivity of the covalent K-Ras(G12D
 ) inhibitors both in vitro and in vivo.  \n\nHosted by the Department of 
 Chemistry
DURATION:PT1H
DTSTAMP:20231218T182616Z
DTSTART;TZID=America/New_York:20240112T133000
LAST-MODIFIED:20231218T182616Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Next-generation precision medicine through covalent reactivity: fr
 om click chemistry to ‘undruggable’ targets
UID:CAL-8a018ccf-8b87f80e-018c-7e2dc1c7-00001ab3demobedework@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=Research:/user/public-user/T
 opics/Research
X-BEDEWORK-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Natural Sciences:/user/publi
 c-user/Topics/Natural Sciences
X-BEDEWORK-SPEAKER:Qinheng Zheng\, University of California San Francisco
X-BEDEWORK-DUKE-SERIES:Chemistry Seminar Series
X-BEDEWORK-STUDENT-CONTACT;X-BEDEWORK-PARAM-EMAIL=c.conti@duke.edu:The Dep
 artment of Chemistry
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:98
X-BEDEWORK-IMAGE-X2:1000
X-BEDEWORK-IMAGE-Y2:764.6666666666666
X-BEDEWORK-IMAGE-CROP-WIDTH:1000
X-BEDEWORK-IMAGE-CROP-HEIGHT:666.6666666666666
X-BEDEWORK-IMAGE-ALT-TEXT:Dr. Qinheng Zheng
X-BEDEWORK-SUBMITTEDBY:cconti for Chemistry (agrp_ArtsandSciences_Chemistr
 y)
X-BEDEWORK-IMAGE:/public/Images/Qinheng Zheng_resize_20231218062616PM.jpg
X-BEDEWORK-THUMB-IMAGE:/public/Images/Qinheng Zheng_resize_20231218062616P
 M-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:20231218T180847Z
DESCRIPTION:"Minimally Invasive Neuroelectronics"\n\nNeuroelectronic inter
 faces have enabled significant advances in both fundamental neuroscience 
 research and the treatment of neurological disorders. However\, current n
 euroelectronic devices have a clear trade-off between invasiveness and sp
 atial resolution\, and are unable to achieve seamless integration into th
 e nervous system with cell-type specificity. In this talk\, I will first 
 introduce an ultra-small and flexible endovascular neural probe that can 
 be implanted into sub-100-micron scale blood vessels in the brains of rod
 ents without damaging the brain or vasculature. Second\, I will describe 
 a biochemically functionalized electronic probe that enables cell type- a
 nd neuron subtype-specific targeting and recording in the brain. Third\, 
 I will present a bottom-up approach for constructing neural interfaces fr
 om the cell surface\, where neurons are genetically programmed to express
  membrane-localized enzymes that catalyze in situ assembly of functional 
 materials. Finally\, I will discuss future advances toward clinical trans
 lation of minimally invasive neuroelectronic interfaces capable of long-t
 erm monitoring and treatment of neurological disorders.\n\nHosted by the 
 Department of Chemistry
DURATION:PT1H
DTSTAMP:20231218T180847Z
DTSTART;TZID=America/New_York:20240119T133000
LAST-MODIFIED:20231218T180847Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Minimally Invasive Neuroelectronics
UID:CAL-8a018ccf-8b87f80e-018c-7e1dbec2-00001ab2demobedework@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-ALIAS;X-BEDEWORK-PARAM-DISPLAYNAME=Lecture_Talk:/user/public-us
 er/Lectures_Conferences/Lecture_Talk
X-BEDEWORK-SPEAKER:Dr. Anqi Zhang\, Stanford University
X-BEDEWORK-DUKE-SERIES:Chemistry Seminar Series
X-BEDEWORK-STUDENT-CONTACT;X-BEDEWORK-PARAM-EMAIL=c.conti@duke.edu:The Dep
 artment of Chemistry
X-BEDEWORK-IMAGE-X1:0
X-BEDEWORK-IMAGE-Y1:139
X-BEDEWORK-IMAGE-X2:550
X-BEDEWORK-IMAGE-Y2:505.6666666666667
X-BEDEWORK-IMAGE-CROP-WIDTH:550
X-BEDEWORK-IMAGE-CROP-HEIGHT:366.6666666666667
X-BEDEWORK-IMAGE-ALT-TEXT:Dr. Anqi Zhang
X-BEDEWORK-SUBMITTEDBY:cconti for Chemistry (agrp_ArtsandSciences_Chemistr
 y)
X-BEDEWORK-IMAGE:/public/Images/Anqi_resize_20231218060847PM.jpg
X-BEDEWORK-THUMB-IMAGE:/public/Images/Anqi_resize_20231218060847PM-thumb.p
 ng
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 understanding of microbes has transformed in recent decade
 s. The explosion of microbiome research has led to the discovery of micro
 bes that play key roles in human\, animal\, and ecological health\, agric
 ulture\, industry\, and infrastructure. Microbes with properties of inter
 est are being discovered more rapidly than they can be studied with curre
 nt methods. Our group is working to increase the pace of study by develop
 ing new bioinformatic methods that leverage high-throughput sequencing fo
 r microbial genomics and microbiome research\, with a particular focus on
  non-model microbes. I will focus on a medium-throughput method for pheno
 type-genotype mapping\, and our epigenetic in a non-model fungal pathogen
  and microbial communities.
DURATION:PT1H
DTSTAMP:20240110T144514Z
DTSTART;TZID=America/New_York:20240122T120000
LAST-MODIFIED:20240110T144514Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:The Microbes Less Traveled: Genomic Technologies for Non-model Mic
 robes
UID:CAL-8a018ccf-8b87f80e-018c-f3cf0669-00002ab9demobedework@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:Josh Granek
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:Josh Granek\, PhD\, Assistant Professor\, Depart
 ment 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/Josh Granek_20240110024514PM.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Josh Granek_20240110024514PM-thumb.p
 ng
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:While much of the cutting edge work in omics data analysis and
  modeling is still mainly in academia\, biotechs and pharma are very adva
 nced\, and in some cases leading\, in areas related to molecular design a
 nd clinical data analysis. I have been leading the AI / ML work for R&D a
 t one of the largest pharma companies for almost two years and will share
  some of the methods we have been developing and using to address computa
 tional challenges across all stages of the drug discovery and development
  process. I will also share some of the lessons I have learned over this 
 period.
DURATION:PT1H
DTSTAMP:20240119T163702Z
DTSTART;TZID=America/New_York:20240129T120000
LAST-MODIFIED:20240119T163702Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:AI / ML in Big Pharma – Omics\, Molecular Design and Clinical Data
  Analysis
UID:CAL-8a0292fd-8d13410f-018d-2293ea66-00006432demobedework@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:Ziv Bar-Joseph
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:Ziv Bar-Joseph\, PhD\, VP and Head of R&amp\;amp
 \;D Data and Computational Sciences at Sanofi and the FORE Systems Profes
 sor of Machine Learning Department and Computational Biology in the Schoo
 l of Computer Science at Carnegie Mellon University
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Ziv Bar-Joseph canva photo_20240119043535P
 M.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Ziv Bar-Joseph canva photo_202401190
 43535PM-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:Fran's research interests are in large part focused on underst
 anding local mutation rate heterogeneity across the human genome using ca
 ncer genomic data analyses. The Supek lab studies the underlying causes o
 f this variation in local mutation risk\, in particular differential DNA 
 repair and how this relates to chromatin organization and how it varies b
 etween individuals.
DURATION:PT1H
DTSTAMP:20240129T195120Z
DTSTART;TZID=America/New_York:20240205T120000
LAST-MODIFIED:20240129T195120Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Distribution of Mutation Risk Across the Human Genome
UID:CAL-8a0292fd-8d13410f-018d-564a7840-00003135demobedework@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:Fran Supek
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:Fran Supek\, PhD\, is a Group Leader at IRB Barc
 elona and a Professor at BRIC\, University of Copenhagen
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Fran Supek canva photo_20240129053537PM.pn
 g
X-BEDEWORK-THUMB-IMAGE:/public/Images/Fran Supek canva photo_2024012905353
 7PM-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:Recent advances in single-cell sequencing have revealed hetero
 geneous cell types in the non-cancerous cells infiltrating tumors\, which
  affects cancer progression and therapy responses. The integration of mul
 tiple scRNA-seq datasets across tumors can reveal common cell types and s
 tates in the tumor microenvironment (TME). We developed a data-driven fra
 mework\, MetaTiME\, which uses machine learning on millions of TME single
  cells\, to learn "meta-components" that can interpret independent gene e
 xpression variations representing cell types\, cell states\, and signalin
 g activities. The meta-components depict functionally distinct gene progr
 ams and reveal TME cell states and their gene regulation with higher gran
 ularity. Following the idea of transfer learning\, by projecting onto the
  MetaTiME space\, we create a tool that annotates cell states and signatu
 re continuums for TME scRNA-seq data. Overall\, MetaTiME learns data-driv
 en meta-components that depict cellular states and gene regulators useful
  for studies in tumor immunity and cancer immunotherapy.
DURATION:PT1H
DTSTAMP:20240207T211157Z
DTSTART;TZID=America/New_York:20240219T120000
LAST-MODIFIED:20240207T211157Z
LOCATION;X-BEDEWORK-UID=18832edc-1c2ecfef-011c-481f44ec-0000030a:French Fa
 mily Science Center 4233
STATUS:CONFIRMED
SUMMARY:Data-Driven Understanding of the Single-Cell Space in Tumor Microe
 nvironment
UID:CAL-8a0292fd-8d13410f-018d-8568a8b5-0000606ddemobedework@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:Yi Zhang
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:Assistant Professor\, Neurosurgery\, Duke Univer
 sity
X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
 s (CBB) (agrp_SchoolofMedicine_CBB)
X-BEDEWORK-IMAGE:/public/Images/Yi Zhang canva photo_20240207091044PM.png
X-BEDEWORK-THUMB-IMAGE:/public/Images/Yi Zhang canva photo_20240207091044P
 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: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
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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
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 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
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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
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:Ricardo Henao
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: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
 -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: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
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X-BEDEWORK-SPEAKER:John Hickey
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
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X-BEDEWORK-IMAGE-ALT-TEXT:Dr. John Hickey\, PhD\, Assistant Professor in B
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X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
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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: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
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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
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 icine,":Biomedical Engineering (BME)\,Biostatistics and Bioinformatics\,D
 uke Center for Genomic and Computational Biology (GCB)\,Precision Genomic
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X-BEDEWORK-SPEAKER:Ravi Madduri
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:Dr. Ravi Madduri\, PhD\, Senior Computer Scienti
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X-BEDEWORK-SUBMITTEDBY:monicaf for Computational Biology and Bioinformatic
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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: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
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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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 icine,":Biomedical Engineering (BME)\,Biostatistics and Bioinformatics\,D
 uke Center for Genomic and Computational Biology (GCB)\,Precision Genomic
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X-BEDEWORK-SPEAKER:Monica Agrawal
X-BEDEWORK-DUKE-SERIES:CBB Monday Seminar Series
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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: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
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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: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
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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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 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
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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)
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END:VEVENT
END:VCALENDAR

