Artifact trim-galore_0.6.10-1_all

Metadata
deb_control_files:
- control
- md5sums
deb_fields:
  Architecture: all
  Depends: perl:any, cutadapt
  Description: |-
    automate quality and adapter trimming for DNA sequencing
     Trim Galore! is a wrapper script to automate quality and adapter trimming
     as well as quality control, with some added functionality to remove
     biased methylation positions for RRBS sequence files (for directional,
     non-directional (or paired-end) sequencing). It's main features are:
      * For adapter trimming, Trim Galore! uses the first 13 bp of Illumina
        standard adapters ('AGATCGGAAGAGC') by default (suitable for both ends
        of paired-end libraries), but accepts other adapter sequence, too
      * For MspI-digested RRBS libraries, Trim Galore! performs quality and
        adapter trimming in two subsequent steps. This allows it to remove
        2 additional bases that contain a cytosine which was artificially
        introduced in the end-repair step during the library preparation
      * For any kind of FastQ file other than MspI-digested RRBS, Trim
        Galore! can perform single-pass adapter- and quality trimming
      * The Phred quality of basecalls and the stringency for adapter removal
        can be specified individually
      * Trim Galore! can remove sequences if they become too short during
        the trimming process. For paired-end files Trim Galore! removes entire
        sequence pairs if one (or both) of the two reads became shorter than
        the set length cutoff. Reads of a read-pair that are longer than a
        given threshold but for which the partner read has become too short
        can optionally be written out to single-end files. This ensures that
        the information of a read pair is not lost entirely if only one read
        is of good quality
      * Trim Galore! can trim paired-end files by 1 additional bp from the 3'
        end of all reads to avoid problems with invalid alignments with Bowtie 1
      * Trim Galore! accepts and produces standard or gzip compressed FastQ files
      * FastQC can optionally be run on the resulting output files once
        trimming has completed
  Homepage: https://www.bioinformatics.babraham.ac.uk/projects/trim_galore/
  Installed-Size: '17528'
  Maintainer: Debian Med Packaging Team <debian-med-packaging@lists.alioth.debian.org>
  Package: trim-galore
  Priority: optional
  Recommends: fastqc
  Section: science
  Version: 0.6.10-1
srcpkg_name: trim-galore
srcpkg_version: 0.6.10-1

File

trim-galore_0.6.10-1_all.deb
File too big (17.0 MB > 2.0 MB): you can view it raw or download it instead.

Relations

Relation Direction Type Name
built-using Source package trim-galore_0.6.10-1

binary package System - - 6 months, 1 week ago 5 months, 1 week
BETA