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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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2017
Materias:
Resource
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5538560/
https://www.ncbi.nlm.nih.gov/pubmed/28522612
http://dx.doi.org/10.1101/gr.211656.116

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5538560/
https://www.ncbi.nlm.nih.gov/pubmed/28522612
http://dx.doi.org/10.1101/gr.211656.116

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