Implicating Sequence Variants in Human Disease: Welcome and Introductions - Daniel MacArthur
Implicating Sequence Variants in Human Diseases: Moderated Discussion
Welcome and Introductions - Teri Manolio and Eric Boerwinkle
Integrated Approach: How can we sum across different classes of evidence to assess...
Clinical Implications: How could these guidelines be used in context of diagnostic-decision-making?
Leveraging Massive-Scale Databases of Human Genetic Variation - Daniel MacArthur
MPG Primer: Structural Variation (2015)
Statistical Analysis: How can we robustly identify variants underlying disease?
Revisions (as needed) to Plans for Day's Discussions - Daniel MacArthur
Experimental Data: How can we investigate whether candidate causal variants...
MPG Primer: ExAC & gnomAD: Using large genomic data sets to interpret human genetic variation (2017)
GM4: Welcome, Introductions - Teri Manolio and Marc Williams
Study Design: What sample selection and data processing procedures maximize...
Beckett asks Prof Daniel MacArthur about data science
Supporting Genomics in the Practice of Medicine by Heidi Rehm, PhD, FACMG
Heidi Rehm presents “Deciphering the Genome: Community Driven Approaches”
Genomics, Big Data, and Medicine Seminar Series – Daniel MacArthur
Midsummer Nights' Science: Using big data to understand rare diseases (2016)
ClinAction Workshop: Towards Genome Medicine: UK Perspective - Timothy Hubbard
Symposium, 2012, Impact of Molecular Biology, Prof. Stylianos E. Antonarakis
