GenomeVIP: a cloud platform for genomic variant discovery and interpretation

Identifying genomic variants is a fundamental first step toward the understanding of the role of inherited and acquired variation in disease. The accelerating growth in the corpus of sequencing data that underpins such analysis is making the data-download bottleneck more evident, placing substantial...

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Dades bibliogràfiques
Publicat a:Genome Res
Autors principals: Mashl, R. Jay, Scott, Adam D., Huang, Kuan-lin, Wyczalkowski, Matthew A., Yoon, Christopher J., Niu, Beifang, DeNardo, Erin, Yellapantula, Venkata D., Handsaker, Robert E., Chen, Ken, Koboldt, Daniel C., Ye, Kai, Fenyö, David, Raphael, Benjamin J., Wendl, Michael C., Ding, Li
Format: Artigo
Idioma:Inglês
Publicat: Cold Spring Harbor Laboratory Press 2017
Matèries:
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5538560/
https://ncbi.nlm.nih.gov/pubmed/28522612
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.211656.116
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