Mercurial > repos > peterjc > fastq_paired_unpaired
view tools/fastq/fastq_paired_unpaired.txt @ 0:72e9fcaec61f
Migrated tool version 0.0.4 from old tool shed archive to new tool shed repository
author | peterjc |
---|---|
date | Tue, 07 Jun 2011 17:21:17 -0400 |
parents | |
children | 7ed81e36fc1c |
line wrap: on
line source
Galaxy tool to divide FASTQ files into paired and unpaired reads ================================================================ This tool is copyright 2010 by Peter Cock, SCRI, UK. All rights reserved. See the licence text below. This tool is a short Python script (using the Biopython library functions) which divides a FASTQ file into paired reads, and single or orphan reads. You can have separate files for the forward/reverse reads, or have them interleaved in a single file. Note that the FASTQ variant is unimportant (Sanger, Solexa, Illumina, or even Color Space should all work equally well). There are just two files to install: * fastq_paired_unpaired.py (the Python script) * fastq_paired_unpaired.xml (the Galaxy tool definition) The suggested location is in the Galaxy folder tools/fastq next to other FASTQ tools provided with Galaxy. You will also need to modify the tools_conf.xml file to tell Galaxy to offer the tool. One suggested location is next to the fastq_filter.xml entry. Simply add the line: <tool file="fastq/fastq_paired_unpaired.xml" /> That's it. History ======= v0.0.1 - Initial version, using Biopython v0.0.2 - Help text; cope with multiple pairs per template v0.0.3 - Galaxy XML wrappers added v0.0.4 - Use Galaxy library to handle FASTQ files (avoid Biopython dependency) Developers ========== This script and other tools for filtering FASTA, FASTQ and SFF files are currently being developed on the following hg branch: http://bitbucket.org/peterjc/galaxy-central/src/fasta_filter For making the "Galaxy Tool Shed" http://community.g2.bx.psu.edu/ tarball use the following command from the Galaxy root folder: tar -czf fastq_paired_unpaired.tar.gz tools/fastq/fastq_paired_unpaired.* Check this worked: $ tar -tzf fastq_paired_unpaired.tar.gz fastq/fastq_paired_unpaired.py fastq/fastq_paired_unpaired.txt fastq/fastq_paired_unpaired.xml Licence (MIT/BSD style) ======================= Permission to use, copy, modify, and distribute this software and its documentation with or without modifications and for any purpose and without fee is hereby granted, provided that any copyright notices appear in all copies and that both those copyright notices and this permission notice appear in supporting documentation, and that the names of the contributors or copyright holders not be used in advertising or publicity pertaining to distribution of the software without specific prior permission. THE CONTRIBUTORS AND COPYRIGHT HOLDERS OF THIS SOFTWARE DISCLAIM ALL WARRANTIES WITH REGARD TO THIS SOFTWARE, INCLUDING ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS, IN NO EVENT SHALL THE CONTRIBUTORS OR COPYRIGHT HOLDERS BE LIABLE FOR ANY SPECIAL, INDIRECT OR CONSEQUENTIAL DAMAGES OR ANY DAMAGES WHATSOEVER RESULTING FROM LOSS OF USE, DATA OR PROFITS, WHETHER IN AN ACTION OF CONTRACT, NEGLIGENCE OR OTHER TORTIOUS ACTION, ARISING OUT OF OR IN CONNECTION WITH THE USE OR PERFORMANCE OF THIS SOFTWARE.