GrabBlur - a framework to facilitate the secure exchange of whole-exome and -genome SNV data using VCF files

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...

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Detalles Bibliográficos
Autores principales: Stade, Björn, Seelow, Dominik, Thomsen, Ingo, Krawczak, Michael, Franke, Andre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4083413/
https://www.ncbi.nlm.nih.gov/pubmed/25055742
http://dx.doi.org/10.1186/1471-2164-15-S4-S8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4083413/
https://www.ncbi.nlm.nih.gov/pubmed/25055742
http://dx.doi.org/10.1186/1471-2164-15-S4-S8

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