NHGRI's Current Approach to "Variant to Function to Disease" - Adam Felsenfeld

NHGRI's Current Approach to "Variant to Function to Disease" - Adam FelsenfeldПодробнее

NHGRI's Current Approach to "Variant to Function to Disease" - Elise FeingoldПодробнее

Element 1: Understanding the Genetic Architecture of Health and Disease at Scale - Adam FelsenfeldПодробнее

From Genome to Phenotype (Summation of the Meeting) - Adam FelsenfeldПодробнее

Update on the Genome Sequencing Program - Adam Felsenfeld and Chris WellingtonПодробнее

Concept Clearance: Common Disease Variant Discovery (CDVD) - Adam FelsenfeldПодробнее

Future Opportunities for Genome Sequencing and Beyond Workshop Report - Adam FelsenfeldПодробнее

Genome Sequencing Program Update: Disease 2020 - Adam FelsenfeldПодробнее

Opportunities for Synergy between the NHGRI Genome Sequencing Program and TOPMed - Adam FelsenfeldПодробнее

How to Achieve the Science (Four Topics) - Adam FelsenfeldПодробнее

The Forefront of GenomicsПодробнее

Genome Sequencing Program Coordinating Center - Adam FelsenfeldПодробнее

Concept Clearance - RFA Renewal: Human Genome Reference Program - Adam FelsenfeldПодробнее

Comparative and Evolutionary Genomics - Adam FelsenfeldПодробнее

Genome Sequencing Program Analysis Satellites - Adam FelsenfeldПодробнее

Connecting variants to function (V2F)Подробнее

NHGRI Short Course in GenomicsПодробнее

GenomicsПодробнее

Concept Clearance: Genome Sequencing Program Coordinating Center (GSPCC) - Adam FelsenfeldПодробнее

Determining the functional consequences of variants ... Kelly Frazer and Wendy ChungПодробнее