Pasha: a versatile R package for piling chromatin HTS data.
basic_science · Level V
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- Record sourced from PubMed, PMID 27153642.
- Also identified by DOI 10.1093/bioinformatics/btw206.
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Abstract
We describe an R package designed for processing aligned reads from chromatin-oriented high-throughput sequencing experiments. Pasha (preprocessing of aligned sequences from HTS analyses) allows easy manipulation of aligned reads from short-read sequencing technologies (ChIP-seq, FAIRE-seq, MNase-Seq, …) and offers innovative approaches such as ChIP-seq reads elongation, nucleosome midpoint piling strategy for positioning analyses, or the ability to subset paired-end reads by groups of insert size that can contain biologically relevant information. Pasha is a multi-platform R package, available on CRAN repositories under GPL-3 license (https://cran.r-project.org/web/packages/Pasha/). rfenouil@gmail.com or jean-christophe.andrau@igmm.cnrs.fr Supplementary data are available at Bioinformatics online.
Medical subject headings
- Chromatin
- High-Throughput Nucleotide Sequencing
- Software