annotate tools/fastq/fastq_paired_unpaired.txt @ 1:7ed81e36fc1c

Uploaded v0.0.5 which handles Illumina 1.8 style pair naming.
author peterjc
date Mon, 12 Dec 2011 11:33:10 -0500
parents 72e9fcaec61f
children 95a632a71951
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1 Galaxy tool to divide FASTQ files into paired and unpaired reads
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2 ================================================================
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3
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4 This tool is copyright 2010 by Peter Cock, SCRI, UK. All rights reserved.
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5 See the licence text below.
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6
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7 This tool is a short Python script (using the Biopython library functions) which
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8 divides a FASTQ file into paired reads, and single or orphan reads. You can have
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9 separate files for the forward/reverse reads, or have them interleaved in a
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10 single file.
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11
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12 Note that the FASTQ variant is unimportant (Sanger, Solexa, Illumina, or even
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13 Color Space should all work equally well).
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14
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15 There are just two files to install:
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16
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17 * fastq_paired_unpaired.py (the Python script)
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18 * fastq_paired_unpaired.xml (the Galaxy tool definition)
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19
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20 The suggested location is in the Galaxy folder tools/fastq next to other FASTQ
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21 tools provided with Galaxy.
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22
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23 You will also need to modify the tools_conf.xml file to tell Galaxy to offer
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24 the tool. One suggested location is next to the fastq_filter.xml entry. Simply
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25 add the line:
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27 <tool file="fastq/fastq_paired_unpaired.xml" />
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29 That's it.
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32 History
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33 =======
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34
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35 v0.0.1 - Initial version, using Biopython
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36 v0.0.2 - Help text; cope with multiple pairs per template
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37 v0.0.3 - Galaxy XML wrappers added
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38 v0.0.4 - Use Galaxy library to handle FASTQ files (avoid Biopython dependency)
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7ed81e36fc1c Uploaded v0.0.5 which handles Illumina 1.8 style pair naming.
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39 v0.0.5 - Handle Illumina 1.8 style pair names
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41
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42 Developers
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43 ==========
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44
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45 This script and other tools for filtering FASTA, FASTQ and SFF files are
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46 currently being developed on the following hg branch:
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47 http://bitbucket.org/peterjc/galaxy-central/src/fasta_filter
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49 For making the "Galaxy Tool Shed" http://community.g2.bx.psu.edu/ tarball use
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50 the following command from the Galaxy root folder:
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51
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52 tar -czf fastq_paired_unpaired.tar.gz tools/fastq/fastq_paired_unpaired.*
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54 Check this worked:
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55
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56 $ tar -tzf fastq_paired_unpaired.tar.gz
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57 fastq/fastq_paired_unpaired.py
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58 fastq/fastq_paired_unpaired.txt
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59 fastq/fastq_paired_unpaired.xml
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61
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62 Licence (MIT/BSD style)
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63 =======================
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64
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65 Permission to use, copy, modify, and distribute this software and its
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66 documentation with or without modifications and for any purpose and
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67 without fee is hereby granted, provided that any copyright notices
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68 appear in all copies and that both those copyright notices and this
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69 permission notice appear in supporting documentation, and that the
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70 names of the contributors or copyright holders not be used in
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71 advertising or publicity pertaining to distribution of the software
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72 without specific prior permission.
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73
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74 THE CONTRIBUTORS AND COPYRIGHT HOLDERS OF THIS SOFTWARE DISCLAIM ALL
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75 WARRANTIES WITH REGARD TO THIS SOFTWARE, INCLUDING ALL IMPLIED
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76 WARRANTIES OF MERCHANTABILITY AND FITNESS, IN NO EVENT SHALL THE
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77 CONTRIBUTORS OR COPYRIGHT HOLDERS BE LIABLE FOR ANY SPECIAL, INDIRECT
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78 OR CONSEQUENTIAL DAMAGES OR ANY DAMAGES WHATSOEVER RESULTING FROM LOSS
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79 OF USE, DATA OR PROFITS, WHETHER IN AN ACTION OF CONTRACT, NEGLIGENCE
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80 OR OTHER TORTIOUS ACTION, ARISING OUT OF OR IN CONNECTION WITH THE USE
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81 OR PERFORMANCE OF THIS SOFTWARE.