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Repository sample_seqs
Name: sample_seqs
Owner: peterjc
Synopsis: Sub-sample sequences files (e.g. to reduce coverage)
Takes an input file of sequences (typically FASTA or FASTQ, but also
Standard Flowgram Format (SFF) is supported), and returns a new sequence
file sub-sampling from this (in the same format).
Type: unrestricted
Revision: 10:bdaefd241921
This revision can be installed: True
Times cloned / installed: 1354

Repository README files - may contain important installation or license information

Galaxy tool to sub-sample sequence files

This tool is copyright 2014-2023 by Peter Cock, The James Hutton Institute (formerly SCRI, Scottish Crop Research Institute), UK. All rights reserved. See the licence text below (MIT licence).

This tool is a short Python script (using Biopython library functions) to sub-sample sequence files (in a range of formats including FASTA, FASTQ, and SFF). This can be useful for preparing a small sample of data to test or time a new pipeline, or for reducing the read coverage in a de novo assembly.

This tool is available from the Galaxy Tool Shed at:

Automated Installation

This should be straightforward using the Galaxy Tool Shed, which should be able to automatically install the dependency on Biopython, and then install this tool and run its unit tests.

Manual Installation

There are just two files to install to use this tool from within Galaxy:

  • sample_seqs.py (the Python script)
  • sample_seqs.xml (the Galaxy tool definition)

The suggested location is in a dedicated tools/sample_seqs folder.

You will also need to modify the tools_conf.xml file to tell Galaxy to offer the tool. One suggested location is in the filters section. Simply add the line:

<tool file="sample_seqs/sample_seqs.xml" />

You will also need to install Biopython 1.62 or later.

If you wish to run the unit tests, also move/copy the test-data/ files under Galaxy's test-data/ folder. Then:

./run_tests.sh -id sample_seqs

That's it.

History

Version Changes
v0.0.1
  • Initial version.
v0.1.1
  • Using optparse to provide a proper Python command line API.
v0.1.2
  • Interleaved mode for working with paired records.
  • Tool definition now embeds citation information.
v0.2.0
  • Option to give number of sequences (or pairs) desired. This works by first counting all your sequences, then calculates the percentage required in order to sample them uniformly (evenly). This makes two passes through the input and is therefore slower.
v0.2.1
  • Was missing a file for the functional tests.
  • Included testing of stdout messages.
  • Includes testing of failure modes.
v0.2.2
  • Reorder XML elements (internal change only).
  • Use format_source=... tag.
  • Planemo for Tool Shed upload (.shed.yml, internal change only).
v0.2.3
  • Do the Biopython imports at the script start (internal change only).
  • Clarify paired read example in help text.
v0.2.4
  • Depends on Biopython 1.67 via legacy Tool Shed package or bioconda.
  • Style changes to Python code (internal change only).
v0.2.5
  • Use <command detect_errors="aggressive"> (internal change only).
  • Single quote command line arguments (internal change only).
v0.2.6
  • Bumped Biopython dependency version for Python 3 fixes.

Developers

This script and related tools are being developed on this GitHub repository: https://github.com/peterjc/pico_galaxy/tree/master/tools/sample_seqs

For pushing a release to the test or main "Galaxy Tool Shed", use the following Planemo commands (which requires you have set your Tool Shed access details in ~/.planemo.yml and that you have access rights on the Tool Shed):

$ planemo shed_update -t testtoolshed --check_diff tools/sample_seqs/
...

or:

$ planemo shed_update -t toolshed --check_diff tools/sample_seqs/
...

To just build and check the tar ball, use:

$ planemo shed_upload --tar_only tools/sample_seqs/
...
$ tar -tzf shed_upload.tar.gz
test-data/MID4_GLZRM4E04_rnd30_frclip.pair_sample_N5.sff
test-data/MID4_GLZRM4E04_rnd30_frclip.sff
test-data/MID4_GLZRM4E04_rnd30_frclip.sample_C1.sff
test-data/MID4_GLZRM4E04_rnd30_frclip.sample_N5.sff
test-data/MID4_GLZRM4E04_rnd30_frclip.pair_sample_N5.sff
test-data/ecoli.fastq
test-data/ecoli.pair_sample_N100.fastq
test-data/ecoli.sample_C10.fastq
test-data/ecoli.sample_N100.fastq
test-data/get_orf_input.Suis_ORF.prot.fasta
test-data/get_orf_input.Suis_ORF.prot.pair_sample_C10.fasta
test-data/get_orf_input.Suis_ORF.prot.pair_sample_N100.fasta
test-data/get_orf_input.Suis_ORF.prot.sample_C10.fasta
test-data/get_orf_input.Suis_ORF.prot.sample_N100.fasta
tools/sample_seqs/README.rst
tools/sample_seqs/sample_seqs.py
tools/sample_seqs/sample_seqs.xml
tools/sample_seqs/tool_dependencies.xml

Licence (MIT)

Permission is hereby granted, free of charge, to any person obtaining a copy of this software and associated documentation files (the "Software"), to deal in the Software without restriction, including without limitation the rights to use, copy, modify, merge, publish, distribute, sublicense, and/or sell copies of the Software, and to permit persons to whom the Software is furnished to do so, subject to the following conditions:

The above copyright notice and this permission notice shall be included in all copies or substantial portions of the Software.

THE SOFTWARE IS PROVIDED "AS IS", WITHOUT WARRANTY OF ANY KIND, EXPRESS OR IMPLIED, INCLUDING BUT NOT LIMITED TO THE WARRANTIES OF MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE AND NONINFRINGEMENT. IN NO EVENT SHALL THE AUTHORS OR COPYRIGHT HOLDERS BE LIABLE FOR ANY CLAIM, DAMAGES OR OTHER LIABILITY, WHETHER IN AN ACTION OF CONTRACT, TORT OR OTHERWISE, ARISING FROM, OUT OF OR IN CONNECTION WITH THE SOFTWARE OR THE USE OR OTHER DEALINGS IN THE SOFTWARE.

Contents of this repository

Name Description Version Minimum Galaxy Version
e.g. to reduce coverage 0.2.6 16.01

Categories
Assembly - Tools for working with assemblies
Fasta Manipulation - Tools for manipulating fasta data
Fastq Manipulation - Tools for manipulating fastq data
Sequence Analysis - Tools for performing Protein and DNA/RNA analysis