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. AVAILABILITY AND IMPLEMENTATION: Pasha is a multi-platform R package, available on CRAN repositories under GPL-3 license (https://cran.r-project.org/web/packages/Pasha/). CONTACTS: firstname.lastname@example.org or email@example.com SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Pasha: a versatile R package for piling chromatin HTS data
Fenouil, R.; Descostes, N.; Spinelli, L.; Koch, F.; Maqbool, M. A.; Benoukraf, T.; Cauchy, P.; Innocenti, C.; Ferrier, P.; Andrau, J. C.
2016-08-15 / vol 32 / pages 2528-30
1367-4811 (Electronic) 1367-4803 (Linking)
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