fastx-toolkit 0.0.13.1-1 source package in Ubuntu
Changelog
fastx-toolkit (0.0.13.1-1) unstable; urgency=low * New upstream release (Closes: #626761). * Incremented Standards-Version to reflect conformance with Policy 3.9.2 (debian/control, no changes needed). * Corrected Vcs-Git URL (debian/control). -- Charles Plessy <email address hidden> Fri, 08 Jul 2011 13:11:37 +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 | Published | Component | Section | |
|---|---|---|---|---|
| Precise | release | universe | science |
Downloads
| File | Size | SHA-256 Checksum |
|---|---|---|
| fastx-toolkit_0.0.13.1-1.dsc | 2.0 KiB | 49ca3e6cf90f1bb01431dcc3bba5de8ace1d6414c46cbaec576f06b380ce38b4 |
| fastx-toolkit_0.0.13.1.orig.tar.bz2 | 1.1 MiB | 7e1dddd6d56bf148e82d0ef7d5efae7ce62d3419ecb5077f9199a527a5366c90 |
| fastx-toolkit_0.0.13.1-1.debian.tar.gz | 14.0 KiB | 2ea1acbfce059c312060b89443d200790489c3b332eaf6f21bf80d94023ac407 |
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.
