SeqHBase: a big data toolset for family based sequencing data analysis

BACKGROUND: Whole-genome sequencing (WGS) and whole-exome sequencing (WES) technologies are increasingly used to identify disease-contributing mutations in human genomic studies. It can be a significant challenge to process such data, especially when a large family or cohort is sequenced. Our object...

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Detalles Bibliográficos
Autores principales: He, Min, Person, Thomas N, Hebbring, Scott J, Heinzen, Ethan, Ye, Zhan, Schrodi, Steven J, McPherson, Elizabeth W, Lin, Simon M, Peissig, Peggy L, Brilliant, Murray H, O'Rawe, Jason, Robison, Reid J, Lyon, Gholson J, Wang, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2015
Materias:
Methods
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382803/
https://www.ncbi.nlm.nih.gov/pubmed/25587064
http://dx.doi.org/10.1136/jmedgenet-2014-102907

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382803/
https://www.ncbi.nlm.nih.gov/pubmed/25587064
http://dx.doi.org/10.1136/jmedgenet-2014-102907

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