Mercurial > repos > gandres > vcftools_filter_stats_diversity

<tool id="sniplay_vcftoolsslidingwindow" name="VCF tools SlidingWindow" version="1.0.0">

    <!-- [REQUIRED] Tool description displayed after the tool name -->
    <description> Make diversity computation with sliding window </description>

    <!-- [OPTIONAL] 3rd party tools, binaries, modules... required for the tool to work -->
    <requirements>
        <requirement type="binary">perl</requirement>
	<requirement type="package" version="0.1.12b">vcftools</requirement>
    </requirements>

    <!-- [OPTIONAL] Command to be executed to get the tool's version string -->
    <version_command>
<!--
        tool_binary -v
-->
    </version_command>

    <!-- [REQUIRED] The command to execute -->
    <command interpreter="perl">
	VCFToolsSlidingWindow.pl --input $filein --out $fileout_label --step $step --window $window &amp;&amp; mv ${fileout_label}.vcftools.log $filelog &amp;&amp; mv ${fileout_label}.Tajima.D ${fileout_taj} &amp;&amp; mv ${fileout_label}.TsTv ${fileout_tstv} &amp;&amp; mv ${fileout_label}.windowed.pi ${fileout_windowed} &amp;&amp; mv ${fileout_label}.snpden ${fileout_snp}
    </command>

    <!-- [REQUIRED] Input files and tool parameters -->
    <inputs>
	<param name="filein" type="data" format="vcf" optional="false" label="VCF input" />
	<param name="fileout_label" type="text" value="snp_density" optional="false" label="Output file basename"/>
	<param name="window" type="integer" value="200000" optional="false" label="Window size (in bp)"/>
	<param name="step" type="integer" value="50000" optional="false" label="Step size (in bp)"/>
    </inputs>

    <!-- [REQUIRED] Output files -->
    <outputs>
	<data name="fileout_snp" format="tabular" label="${fileout_label}.snpden" />
	<data name="fileout_taj" format="tabular" label="${fileout_label}.Tajima.D" />
	<data name="fileout_tstv" format="tabular" label="${fileout_label}.TsTv" />
	<data name="fileout_windowed" format="tabular" label="${fileout_label}.windowed.pi" />
	<data name="filelog" format="txt" label="${fileout_label}.log" />
    </outputs>

    <!-- [STRONGLY RECOMMANDED] Exit code rules -->
    <stdio>
        <!-- [HELP] If no exit code rule is defined, the tool will stop if anything is written to STDERR -->
        <exit_code range="1:" level="fatal" />
    </stdio>

    <!-- [OPTIONAL] Tests to be run manually by the Galaxy admin -->
    <tests>
        <!-- [HELP] Test files have to be in the ~/test-data directory -->
        <test>
         <param name="filein" value="sample.vcf" />
         <output name="fileout_annot" file="result.annotation" />
         <output name="fileout_het" file="result.het" />
         <output name="fileout_imiss" file="result.imiss" />
         <output name="fileout_sum" file="result.TsTv.summary" />
         <output name="filelog" file="result.log" />
        </test>
    </tests>

    <!-- [OPTIONAL] Help displayed in Galaxy -->
    <help>

.. class:: infomark

**Authors**     Adam Auton, Petr Danecek and Anthony Marcketta (C++ Module) : VCFtools_

.. _VCFtools: http://vcftools.sourceforge.net

 | **Please cite** "The Variant Call Format and VCFtools", Petr Danecek, Adam Auton, Goncalo Abecasis, Cornelis A. Albers, Eric Banks, Mark A. DePristo, Robert Handsaker, Gerton Lunter, Gabor Marth, Stephen T. Sherry, Gilean McVean, Richard Durbin and 1000 Genomes Project Analysis Group, **Bioinformatics**, 2011

.. class:: infomark

**Galaxy integration** Andres Gwendoline, Institut Français de Bioinformatique.

.. class:: infomark

**Support** For any questions about Galaxy integration, please send an e-mail to support.abims@sb-roscoff.fr

---------------------------------------------------


================
VCF tools filter
================

-----------
Description
-----------

  | Compute statistics on VCF file
  | For further informations on VCFtools, please visite the VCFtools website_.

.. _website: http://vcftools.sourceforge.net

-----------------
Workflow position
-----------------

**Upstream tools**

=========== ========================== =======
Name            output file(s)         format
=========== ========================== =======
=========== ========================== =======


**Downstream tools**

=========== ========================== =======
Name            output file(s)         format
=========== ========================== =======
=========== ========================== =======


----------
Input file
----------

VCF file
	VCF file with all SNPs

----------
Parameters
----------

Output file basename
	Prefix for the output VCF file

------------
Output files
------------

.snpden file
	SNP density along chromosomes (number of variants)

.Tajima.D file
	Tajima's D statistics

.TsTv file
	TsTv (Transition/transversion ratio)
.windowed.pi file
	Nucleotide diversity Pi

.log file

---------------------------------------------------

---------------
Working example
---------------

Input files
===========

VCF file
---------

::

	#fileformat=VCFv4.1
	#FILTER=&lt;ID=LowQual,Description="Low quality">
	#FORMAT=&lt;ID=AD,Number=.,Type=Integer,Description="Allelic depths for the ref and alt alleles in the order listed">
	[...]
	CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO	FORMAT	CATB1
	chr1	2209	.	G	T	213.84	.	AC=2;AF=1.00;AN=2;DP=7;Dels=0.00;FS=0.000;HaplotypeScore=0.0000;MLEAC=2;MLEAF=1.00;MQ=41.50;MQ0=0;QD=30.55;EFF=DOWNSTREAM(MODIFIER||||Cc01g00020|mRNA||GSCOCT00012438001|),UPSTREAM(MODIFIER||||Cc01g00010|mRNA||GSCOCT00012439001|)	GT:AD:DP:GQ:PL	1/1:0,7:7:18:242,18,0


Parameters
==========

Output name -> snp_density


Output files
============

.snpden file
------------

::

	CHROM	BIN_START	SNP_COUNT	VARIANTS/KB
	chr1	0	4955	24.775


.Tajima.D file
--------------

::

	CHROM	BIN_START	N_SNPS	TajimaD
	chr1	0	3737	-nan

.TsTv file
----------

::

	CHROM	BinStart	SNP_count	Ts/Tv
	chr1	0	4928	1.88356

.windowed.pi file
-----------------

::

	CHROM	BIN_START	BIN_END	N_VARIANTS	PI
	chr1	1	200000	3764	0.01882


    </help>
    <citations>
            <!-- [HELP] As DOI or BibTex entry -->
        <citation type="bibtex">
@article{Danecek01082011,
author = {Danecek, Petr and Auton, Adam and Abecasis, Goncalo and Albers, Cornelis A. and Banks, Eric and DePristo, Mark A. and Handsaker, Robert E. and Lunter, Gerton and Marth, Gabor T. and Sherry, Stephen T. and McVean, Gilean and Durbin, Richard and 1000 Genomes Project Analysis Group},
title = {The variant call format and VCFtools},
volume = {27},
number = {15},
pages = {2156-2158},
year = {2011},
doi = {10.1093/bioinformatics/btr330},
abstract ={Summary: The variant call format (VCF) is a generic format for storing DNA polymorphism data such as SNPs, insertions, deletions and structural variants, together with rich annotations. VCF is usually stored in a compressed manner and can be indexed for fast data retrieval of variants from a range of positions on the reference genome. The format was developed for the 1000 Genomes Project, and has also been adopted by other projects such as UK10K, dbSNP and the NHLBI Exome Project. VCFtools is a software suite that implements various utilities for processing VCF files, including validation, merging, comparing and also provides a general Perl API.Availability: http://vcftools.sourceforge.netContact: rd@sanger.ac.uk},
URL = {http://bioinformatics.oxfordjournals.org/content/27/15/2156.abstract},
eprint = {http://bioinformatics.oxfordjournals.org/content/27/15/2156.full.pdf+html},
journal = {Bioinformatics}
}
	</citation>

    </citations>

</tool>
author	gandres
date	Fri, 10 Jul 2015 04:16:17 -0400
parents
children	612066e3f57d