Abstract
Summary: 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.
| Original language | English |
|---|---|
| Pages (from-to) | 2528-2530 |
| Number of pages | 3 |
| Journal | Bioinformatics |
| Volume | 32 |
| Issue number | 16 |
| DOIs | |
| State | Published - 15 Aug 2016 |