2022-2023
|
| January 23, 2023 |
Cole Trapnell, University of Washington |
Whole-embryo Development Genetics at Single Cell Resolution |
| November 17, 2022 |
John Novembre, University of Chicago |
Visualization and Study Design Implications of Geographic Structure in Genetic Data |
| November 2, 2022 |
Elliott Margulies, Illumina |
From First Ever to Every Patient: “An Academic Pushing Clinical Adoption of Genomics
from Industry |
2021-2022
|
| March 15, 2022 |
Mark Daly, University of Helsinki |
Biobanks, Disease Consortia, and the Road Ahead in Human Genetics |
| February 21, 2022 |
Bogdan Pasaniuc, University of California Los Angeles |
Large Uncertainty in Individual Polygenic Risk Score (PRS) Estimation Impacts PRS
Implementation in Personalized Medicine |
| February 9, 2022 |
Michael Epstein, Emory University |
Life Moves Pretty Fast: Lessons Learned from ~20 Years in Academia |
| November 12, 2021 |
Michelle McNulty, Boston Children's Hospital |
Using Transcriptomics to Better Understand the Role of APOL1 in Kidney Disease |
| November 5, 2021 |
Eric Fauman, Pfizer |
Toward a Gold Standard SNP to Gene Set |
| September 17, 2021 |
Mark Reppell, AbbVie Pharmaceuticals |
Leveraging Computational Genomics to Advance a Pharmaceutical Pipeline |
2020-2021
|
| April 13, 2021 |
Lynn Jorde, University of Utah |
Human Mutation Rates: Implications for Health and Disease |
| February 16, 2021 |
Eimear Kenny, Mount Sinai |
Population Genetics in an Era of Genomic Health |
| January 21, 2021 |
Charles Rotimi, National Human Genome Research Institute |
Importance of Diversity in Genome Science and Medicine |
| October 7, 2020 |
Jonathan Pritchard, Stanford University |
Why are Human Complex Traits so Enormously Polygenic? Lessons from Molecular Biomarker
Traits |
2019-2020
|
| November 7, 2019 |
Tuuli Lappalainen, Columbia University |
Functional Variation in the Human Genome: Lessons from the Transcriptome |
| September 19, 2019 |
Mary-Claire King, University of Washington |
Inherited Breast and Ovarian Cancer: from Gene Discovery to Precision Medicine and
Public Health |
2018-2019
|
| April 11, 2019 |
Joanna Mountain, 23andMe |
23andMe's Customer-Powered Research |
| February 22, 2019 |
Kathryn Roeder, University of Pittsburgh Medical Center, Carnegie Mellon University |
Learning From the Transcriptome: Analysis of Single Cell and Bulk RNA Sequence Data |
| October 23, 2018 |
Po-Ru Loh, Harvard School of Public Health, Broad Institute |
Leveraging Long Range Phasint to Detect Mosaicism in Blod at Ultra-low Allelic Fractions |
2017-2018
|
| August 27, 2018 |
Lang Li, Ohio State University |
Learning Health System Working Towards a Home Run for Drug Interaction and Pharmacogenetics |
| April 13, 2018 |
Eric Fauman, Pfizer |
The Use of Human Genetics in the Identification and Prioritization of Therapeutic
Drug Targets |
| April 9, 2018 |
Timothy Thornton, University of Washington |
Challenges and New Approaches for Whole Genome Analysis in Multi-Ethnic Populations |
| April 4, 2018 |
Evan Eichler, University of Washington |
Human Evolution by Segmental Duplication and Structural Variation |
| March 23, 2018 |
Elizabeth Thompson, University of Washington |
Mapping Causal DNA Through the Shared Descent of Genome in Population Samples |
| November 13, 2017 |
Fernando Pardo-Mnauel de Villena, University of North Carolina at Chapel Hill |
Structural Variation and the Evolution of the Mouse Genome |
2016-2017
|
| April 21, 2017 |
Mingyao Li, University of Pennsylvania |
Statistical Issues in Single-cell RNA Sequencing Analysis |
| April 13, 2017 |
Sandrine Dudoit, University of California Berkeley |
Using Single-cell Transcriptome Sequencing to iInfer Olfactory Stem Cell Fate Trajectories |
| April 11, 2017 |
Mike Snyder, Stanford University |
Managing Health and Disease Using Omics Data |
| March 21, 2017 |
Jonathan Terhorst, University of California Berkeley |
Robust and Scalable Inference of Population History and Selection from Hundreds of
Whole Genomes |
| March 10, 2017 |
Claus Ekstrom, University of Copenhagen |
Integrative Data Analysis of the Danish Registries |
| February 23, 2017 |
Lars Fritsche, K.G. Jebsen Center for Genetic Epidemiology |
Exploring the Potential of Genome x Phenome-wide Association Studies |
| February 16, 2017 |
Yun Li, University of North Carolina |
Statistical Methods, Computation Tools, and Visualization of Hi-C Data |
| September 12, 2016 |
Soumya Raychaudhuri, Harvard Medical School |
The Genomics of Immune-mediated Diseases and Traits |
2015-2016
|
| May 5, 2016 |
Kenneth Lange, University of California |
Next Generation Statistical Genetics |
| April 21, 2016 |
Yun Li, University of North Carolina |
DISSCO: Direct Imputation of Summary Statistics Allowing Covariates |
| April 18, 2016 |
Noah Zaitlen, University of California San Francisco |
Methods for Genetic Studies Across Multiple Phenotypes |
| April 14, 2016 |
Hongyu Zhao, Yale University |
Prioritization of Disease-Causing Genetic Variants Through Integrated Analysis of
Association Signals and Genomic Annotations |
| April 5, 2016 |
Andrew Clark, Cornell University |
Training the Genome - the Silver Fox Story |
| February 9, 2016 |
Qing Lu, Michigan State University |
A Generalized Similarity U Test for Multivariate Analysis of Sequencing Data |
| January 12, 2016 |
Jay Shendure, University of Washington |
New Methods in Genetics and Genomics |
| September 28, 2015 |
David Cutler, Emory University |
Quantitative Genetics Theory Informs Our Understanding of Male-Female Differences
in Autism |
