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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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| Autors principals: | , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4083413/ https://ncbi.nlm.nih.gov/pubmed/25055742 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-15-S4-S8 |
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