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...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:BMC Bioinformatics
Hlavní autoři: 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.
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2015
Témata:
Methodology Article
On-line přístup: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
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky