NHGRI's Current Approach to "Variant to Function to Disease" - Adam Felsenfeld
NHGRI's Current Approach to "Variant to Function to Disease" - Elise Feingold
Understanding variant to function research
Topic 1: Discovery and Interpretation of Variation Associated with Human Health.. - Barbara Stranger
How Much More Sequencing? What Should NHGRI Do? Why? - Eric Boerwinkle
Determining the functional consequences of variants ... Kelly Frazer and Wendy Chung
Identify Disease Associated Genetic Variants Via 3D Genomics Structure and Regulatory Landscapes
CCMB Seminar 11/09/2022 - Jesse Engreitz, PhD
Data-driven approaches to define rare genetic diseases
Focus Discussion 1: What can NHGRI do to facilitate bridging molecular and organismal phenotype?
Human Genetics: Where do we want to be in 10 years and how can we get there? - Judy Cho
David Bentley - Genomes for Medicine
The Search for Mendelian Disease Genes: Opportunities Afforded, Lessons Learned - David Valle (2014)
Genome: The GIS Speaker Series - Dr Adam Phillippy
NHGRI DIR Seminar Series - Matthew Harris
Multi-omics in Health and Disease (Session 2)
Common Disease Findings
What will the field of genomics look like in 5-10 years? How will it get there? - Jay Shendure
Long read Genome Sequencing for the Molecular Diagnosis of Neurodevelopmental Disorders
The Genomic Landscape circa 2010
NHGRI's Oral History Collection: Interview with Lynn Jorde
NHGRI DIR Seminar Series - Anna Gloyn
Genome-Scale Sequence Analysis - Tyra Wolfsberg (2014)
Multi-omics in Health and Disease (Session 4)
2021 Jeffrey M. Trent Lecture in Cancer Research - Sharon Plon