Ubuntu
fastx-toolkit package

fastx-toolkit 0.0.13.2-1 source package in Ubuntu

Changelog

fastx-toolkit (0.0.13.2-1) unstable; urgency=low


  1313f16 Imported Upstream version 0.0.13.2
  dbfb3ae Removed debian/patches/gcc-4.7.patch, applied upstream.
  182cd30 Include 7 digits of the commit ID in the changelog entry.
  2ae7b63 Spellchecked common “See also” section of the manpages.
  363856c Verbose Debhelper.

 -- Charles Plessy <email address hidden>  Tue, 15 May 2012 21:02:22 +0900

Upload details

Uploaded by:
Debian Med
Uploaded to:
Sid
Original maintainer:
Debian Med
Architectures:
any
Section:
science
Urgency:
Low Urgency

See full publishing history Publishing

Series Pocket Published Component Section

Downloads

File Size SHA-256 Checksum
fastx-toolkit_0.0.13.2-1.dsc 2.1 KiB e2d7eebc3094c654aaa845327b52424976018d4b787bce9117c0adaf5404969f
fastx-toolkit_0.0.13.2.orig.tar.bz2 532.6 KiB df154f785c35d1f8b6f3568ea80c52f742ec03f75564adfe8e1bb0f8de8b1aed
fastx-toolkit_0.0.13.2-1.debian.tar.gz 16.5 KiB 56819e0573909407b67720c31af53f4bb4242728b40a895d4a7bf69900441735

Available diffs

  • diff from 0.0.13.1-2 to 0.0.13.2-1 (pending)

No changes file available.

Binary packages built by this source

fastx-toolkit: FASTQ/A short nucleotide reads pre-processing tools

 The FASTX-Toolkit is a collection of command line tools for preprocessing
 short nucleotide reads in FASTA and FASTQ formats, usually produced by
 Next-Generation sequencing machines. The main processing of such FASTA/FASTQ
 files is mapping (aligning) the sequences to reference genomes or other
 databases using specialized programs like BWA, Bowtie and many others.
 However, it is sometimes more productive to preprocess the FASTA/FASTQ files
 before mapping the sequences to the genome—manipulating the sequences to
 produce better mapping results. The FASTX-Toolkit tools perform some of these
 preprocessing tasks.