comparison ped2bed/ped2bed.xml @ 1:420b57c3c185 draft

Uploaded

1:420b57c3c185

<tool id="ped2bed" name="plink: ped2bed" version="1.24">
	<description>Convert ped to bed</description>
	<requirements>
		<requirement type="package" version="1.07">plink</requirement>
	</requirements>
	<command interpreter="bash">./ped2bed.sh $ped $map $bed $fam $bim $logs
    </command>
	<inputs>
		<param format="txt" name="ped" type="data" label="Allelic file in PED format" help="Allelic file in PED format"/>
		<param format="txt" name="map" type="data" label="Map file" help="Map file"/>
	</inputs>
	<outputs>
		<data format="txt" name="bed" label="Bed file"/>
		<data format="txt" name="fam" label="Fam file"/>
		<data format="txt" name="bim" label="Bim file"/>
		<data format="txt" name="logs" label="All Logs"/>
	</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 -->
        <!-- [HELP] Multiple tests can be defined with different parameters -->
<!--
        <test>
        </test>
-->
    </tests>
	<help>
	

.. class:: infomark

**Authors** plink_

.. _plink: http://pngu.mgh.harvard.edu/purcell/plink/

  | "PLINK: a toolset for whole-genome association and population-based linkage analysis.", **Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MAR, Bender D, Maller J, Sklar P, de Bakker PIW, Daly MJ, Sham PC.**, American Journal of Human Genetics, 81, 2007.

.. class:: infomark

**Galaxy integration** South Green.

.. class:: infomark

**Please cite** "SNiPlay3: a web-based application for exploration and large scale analyses of genomic variations", **Dereeper A. et al.**, Nucl. Acids Res. (1 july 2015) 43 (W1).


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



=======
Ped2Bed
=======

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

  | PLINK is a free, open-source whole genome association analysis toolset, designed to perform a range of basic, large-scale analyses in a computationally efficient manner.
  | For further informations, please visite the plink website_.

.. _website: http://pngu.mgh.harvard.edu/purcell/plink/


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

**Upstream tool**

=============== ========================== ===========
Name            output file(s)             format 
=============== ========================== ===========
VCFtools filter PED and map files          ped and map
=============== ========================== ===========


**Downstream tool**

=========== ========================== =======
Name            input file(s)          format
=========== ========================== =======
Admixture   Bed, fam and bim file      txt
=========== ========================== =======


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

PED file
	Allelic file in PED format 

MAP file



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

Bed file

Fam file

Bim file

All logs 
	Log file


------------
Dependencies
------------
plink 
	version 1.07

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

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

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

PED file
--------

::
	
	AZUCENA	AZUCENA	0	0	0	0	G	G	A	A	C	C	T	T	T	
	BULUPANDAK	BULUPANDAK	0	0	0	0	G	G	A	A	A	A	T	

MAP file
--------

::
	
	0	Chr1:4299	0	4299
	0	Chr1:26710	0	26710
	0	Chr1:56184	0	56184
	0	Chr1:93272	0	93272


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

Bed file
--------

::

	binary file

Fam file
--------

::

	AZUCENA AZUCENA 0 0 0 -9
	BULUPANDAK BULUPANDAK 0 0 0 -9

Bim file
--------

::

	0	Chr1:4299	0	4299	A	G
	0	Chr8:18058	0	18058	C	T


	</help>
    <citations>
        <!-- [HELP] As DOI or BibTex entry -->
    	<citation type="bibtex">@article{Dereeper03062015,
author = {Dereeper, Alexis and Homa, Felix and Andres, Gwendoline and Sempere, Guilhem and Sarah, Gautier and Hueber, Yann and Dufayard, Jean-François and Ruiz, Manuel}, 
title = {SNiPlay3: a web-based application for exploration and large scale analyses of genomic variations},
year = {2015}, 
doi = {10.1093/nar/gkv351}, 
abstract ={SNiPlay is a web-based tool for detection, management and analysis of genetic variants including both single nucleotide polymorphisms (SNPs) and InDels. Version 3 now extends functionalities in order to easily manage and exploit SNPs derived from next generation sequencing technologies, such as GBS (genotyping by sequencing), WGRS (whole gre-sequencing) and RNA-Seq technologies. Based on the standard VCF (variant call format) format, the application offers an intuitive interface for filtering and comparing polymorphisms using user-defined sets of individuals and then establishing a reliable genotyping data matrix for further analyses. Namely, in addition to the various scaled-up analyses allowed by the application (genomic annotation of SNP, diversity analysis, haplotype reconstruction and network, linkage disequilibrium), SNiPlay3 proposes new modules for GWAS (genome-wide association studies), population stratification, distance tree analysis and visualization of SNP density. Additionally, we developed a suite of Galaxy wrappers for each step of the SNiPlay3 process, so that the complete pipeline can also be deployed on a Galaxy instance using the Galaxy ToolShed procedure and then be computed as a Galaxy workflow. SNiPlay is accessible at http://sniplay.southgreen.fr.}, 
URL = {http://nar.oxfordjournals.org/content/early/2015/06/03/nar.gkv351.abstract}, 
eprint = {http://nar.oxfordjournals.org/content/early/2015/06/03/nar.gkv351.full.pdf+html}, 
journal = {Nucleic Acids Research} 
}

    	</citation>

    </citations>
</tool>