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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4580299/
https://www.ncbi.nlm.nih.gov/pubmed/26395405
http://dx.doi.org/10.1186/s12859-015-0736-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4580299/
https://www.ncbi.nlm.nih.gov/pubmed/26395405
http://dx.doi.org/10.1186/s12859-015-0736-4

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