Pash 3.0: A versatile software package for read mapping and integrative analysis of genomic and epigenomic variation using massively parallel DNA sequencing

BACKGROUND: Massively parallel sequencing readouts of epigenomic assays are enabling integrative genome-wide analyses of genomic and epigenomic variation. Pash 3.0 performs sequence comparison and read mapping and can be employed as a module within diverse configurable analysis pipelines, including...

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Detalles Bibliográficos
Autores principales: Coarfa, Cristian, Yu, Fuli, Miller, Christopher A, Chen, Zuozhou, Harris, R Alan, Milosavljevic, Aleksandar
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001746/
https://www.ncbi.nlm.nih.gov/pubmed/21092284
http://dx.doi.org/10.1186/1471-2105-11-572

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001746/
https://www.ncbi.nlm.nih.gov/pubmed/21092284
http://dx.doi.org/10.1186/1471-2105-11-572

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