Mike is an associate computational biologist working on the preliminary analyses of exomes and genomes to identify causal candidate genes and variants. He also manages datasets from Mendelian disease collaborators. He was previously a Senior Research Associate in the Broad Institute’s Clinical Research Sequencing Platform. […]
Zach is a postdoctoral fellow interested in developing novel methods to measure variant penetrance and understanding the underlying factors that affect variant pathogenicity. @zaczap […]
Alicia is a graduate student from the University of South Australia. She is working on the molecular diagnosis of rare genetic disease, with particular focus on disorders contributing to perinatal mortality. […]
Laurent is now a Sr. Research Scientist in the Computational Genomics at Vertex in San Diego. […]
Irina is a postdoctoral scientist interested in the functional annotation of protein-truncating variants and their impact on human biology. She studied protein function annotation via protein complexes during her PhD at the University of Cambridge, and worked on de novo genome assembly and gene annotation at European Bioinformatics Institute before joining the lab. […]
Harindra is part of the Engineering team at the Broad Center for Mendelian Genomics at ATGU. Prior to that, he worked at the Pasteur Institute in Paris and was with the Cancer group at the Broad Institute of MIT. He works on developing software tools and methods that help study rare genetic diseases. He has […]
Samantha is the clinical project manager at the Broad Institute’s Center for Mendelian Genomics. She is a genetic counselor who has worked in the area of cardiovascular genetics and now focuses on the management and sharing of both clinical and genetic data. […]
Katherine is a computational biologist conducting exome analyses for families with rare disease. Before joining the Broad, she worked in the NIH’s Undiagnosed Diseases Program. […]
Beryl is a research fellow supervised by Daniel MacArthur and Mark Daly. Her research focuses on the integration of functional genomics, specifically transcriptome sequencing into genetic variant interpretation. She received her PhD from the Biological and Biomedical Sciences Program at Harvard Medical School working in the Medical and Population Genetics program and ATGU. twitter handle […]
Daniel worked as a computational analyst focused on investigating the impact of loss-of-function (LoF) variation in healthy humans and developing quantitative methods for assessing the veracity of splice site annotations. He is now a graduate student at Harvard. […]
