Group-based variant calling leveraging next-generation supercomputing for large-scale whole-genome sequencing studies

MOTIVATION: Next-generation sequencing (NGS) technologies have become much more efficient, allowing whole human genomes to be sequenced faster and cheaper than ever before. However, processing the raw sequence reads associated with NGS technologies requires care and sophistication in order to draw c...

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Detalhes bibliográficos
Publicado no:BMC Bioinformatics
Main Authors: Standish, Kristopher A., Carland, Tristan M., Lockwood, Glenn K., Pfeiffer, Wayne, Tatineni, Mahidhar, Huang, C Chris, Lamberth, Sarah, Cherkas, Yauheniya, Brodmerkel, Carrie, Jaeger, Ed, Smith, Lance, Rajagopal, Gunaretnam, Curran, Mark E., Schork, Nicholas J.
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2015
Assuntos:
Methodology Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4580299/
https://ncbi.nlm.nih.gov/pubmed/26395405
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-015-0736-4
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