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The Center will provide exome and/or whole­ genome sequencing at no cost to the collaborator for affected cases and relatives. This centralized service will offer high­ quality sequencing and analysis at the Broad Institute, incorporating discovery of all classes of variation (including copy number...

All sequencing data produced by the Broad Institute will be made available to collaborators on request. The CMG will make the following data accessible: Array data Acess to array data (if generated for your samples) will be granted via Aspera. Sample BAMs VCF file containing all samples in cohort...

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Current Openings: Thank you for your interest. Please keep an eye on this page for openings. We welcome inquiries from students and experienced scientists at all levels. Please send your inquiries to TRGapplications@broadinstitute.org, and please be sure to include what position you are interested...

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