ClinAction Workshop: Categorizing Variants after Whole Genome Sequencing - Jonathan Berg
ClinAction Workshop: New Resource: NBCI's ClinVar - Donna Maglott
ClinAction Workshop: Towards Genome Medicine: UK Perspective - Timothy Hubbard
ClinAction Workshop: Welcome and Meeting Overview - Eric Green
Sharing Data about Genomic Variants: A Clinical and Scientific Imperative
ClinAction Workshop: Clinical Pharmacogenetics Implementation Consortium of the PGRN - Howard McLeod
ClinAction Workshop: Moderated Discussion - Matthew Hurles
Whole Genome Sequencing for Rare Clinical and Consanguineous Familial Cases
Evaluation of Genomic Applications in Practice and Prevention (EGAPP) - Ned Calonge
ClinAction Workshop: Database Integration - Paul Flicek
Secondary or Incidental Findings from Exome Sequence Data - Jennifer Johnston
Clinical Decision Support for the Whole Genome Sequence
ClinAction Workshop: Coriell Personalized Medicine Collaborative (CPMC) ® - Erynn Gordon
Whole Genome Sequencing, George Church
Group 2: Integrating Genomic Variant Discovery with Function
Presentation from Large-Scale Genome Sequencing and Analysis Centers' Investigators - Eric Lander
ClinAction Workshop: Centers for Medicare and Medicaid Services (CMS) - Jeff Roche
Inferring Intra-Tumor Heterogeneity from Whole-Genome/Exome Sequencing Data - Layla Oesper
Jeff Schloss: Sequencing the human genome to promote health and understand disease
Part A - Summary of the Report
