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Pash 3.0: A versatile software package for read mapping and integrative analysis of genomic and epigenomic variation using massively parallel DNA sequencing
Authors:Cristian Coarfa  Fuli Yu  Christopher A Miller  Zuozhou Chen  R Alan Harris  Aleksandar Milosavljevic
Institution:1.Department of Molecular and Human Genetics,Baylor College of Medicine,Houston,USA;2.The Human Genome Sequencing Center,Baylor College of Medicine,Houston,USA
Abstract:

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 ChIP-Seq and methylome mapping by whole-genome bisulfite sequencing.
Keywords:
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