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Field
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have experience in computational methods development, in human genetics or a different field. Possible areas of research include: 1. Developing methods to compare the genetic architecture of rare vs
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external) Position Summary The Reilly Lab seeks highly motivated Postdoctoral Associates to join an interdisciplinary research program focused on understanding how genetic variants impact human
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leveraging human genetic diversity to improve genetic discovery, fine-mapping, and biological interpretation. The laboratory is currently supported by an NIH Pathway to Independence Award (K99/R00) from
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understand how disruption of genes, transcripts, and regulatory elements produces human disease. A central goal of the laboratory is to move beyond genetic association or variant annotation to
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Research Hospital is seeking a highly motivated Postdoctoral Research Associate to investigate fundamental mechanisms of gene regulation and genetic variation in human hematopoiesis and blood disorders
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underlying human disease, with a major research program focused on genetic hearing loss and the functional biology of the auditory system. We integrate human genetics with molecular biology, genome editing
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disease-associated genetic variants Integration of single-cell multiome data (snATAC + scRNA-seq) with large-scale human genetics Analysis of population-scale datasets and biobanks (e.g., All of Us, UK
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The laboratory combines human endothelial cell culture and perturbation systems with genomic discovery tools to dissect how genetic variation at CAD-associated loci operates through the vessel wall
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posting. Position Type Full-Time/Regular The TCW laboratory ( https://sites.bu.edu/tcwlab/ ) in the Department of Pharmacology, Physiology & Biophysics at Boston University Chobanian & Avedisian School of
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. About the Group: The Martin group works on the genetic basis of rare and common disease, using large-scale human genetic datasets with rich linkage to electronic health records and questionnaires