NHGRI's Current Approach to "Variant to Function to Disease" - Elise Feingold
NHGRI's Current Approach to "Variant to Function to Disease" - Adam Felsenfeld
How Much More Sequencing? What Should NHGRI Do? Why? - Eric Boerwinkle
Understanding variant to function research
Connecting variants to function (V2F)
Determining the functional consequences of variants ... Kelly Frazer and Wendy Chung
Topic 1: Discovery and Interpretation of Variation Associated with Human Health.. - Barbara Stranger
NHGRI DIR Seminar Series - Lars Steinmetz
Variant Annotation Using RegulomeDB and HaploReg - Jill Moore
Genomic Variation and the Inherited Basis of Common Disease
Topic 1 Discussion: Discovery & Interpretation of Variation Associated with Human Health and Disease
Topic 1: Discovery and Interpretation of Variation Associated with Human Health... - Anshul Kundaje
NHGRI DIR Seminar Series - Douglas Fowler
Data-driven approaches to define rare genetic diseases
Group 2: Integrating Genomic Variant Discovery with Function
Moderated Discussion: Variant Discovery and Association - Goncalo Abecasis
From Genome to Phenotype: Welcome and Introduction - Eric Green
PSB 2023 Invited Talk - Erin Ramos - "NHGRI’s Efforts to Advance Genomic Medicine Implementation"
Genomic Approaches to the Study of Complex Genetic Diseases - Karen Mohlke (2016)
Group 1: Understanding the Genetic Architecture of Health and Disease at Scale