Article
GrabBlur--a framework to facilitate the secure exchange of whole-exome and -genome SNV data using VCF files.
BMC genomics - 1 Jan 2014
Stade Björn, Seelow Dominik, Thomsen Ingo, Krawczak Michael, Franke Andre
Abstract excerpt
BACKGROUND: Next Generation Sequencing (NGS) of whole exomes or genomes is increasingly being used in human genetic research and diagnostics. Sharing NGS data with third parties can help physicians and researchers to identify causative or predisposing mutations for a specific sample of interest more efficiently. In many cases, however, the exchange of such data may collide with data privacy regulations. GrabBlur...
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