SAMBLASTER: fast duplicate marking and structural variant read extraction

Motivation: Illumina DNA sequencing is now the predominant source of raw genomic data, and data volumes are growing rapidly. Bioinformatic analysis pipelines are having trouble keeping pace. A common bottleneck in such pipelines is the requirement to read, write, sort and compress large BAM files mu...

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Detalles Bibliográficos
Autores principales: Faust, Gregory G., Hall, Ira M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Applications Notes
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147885/
https://www.ncbi.nlm.nih.gov/pubmed/24812344
http://dx.doi.org/10.1093/bioinformatics/btu314

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147885/
https://www.ncbi.nlm.nih.gov/pubmed/24812344
http://dx.doi.org/10.1093/bioinformatics/btu314

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