Mercurial > repos > wolma > mimodd
view sam_header.xml @ 18:2742ad4d1608 draft
rebase on package_python_3_4_lean
author | wolma |
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date | Tue, 26 Apr 2016 11:21:43 -0400 |
parents | 93db2f9bca12 |
children | c46406466625 |
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<tool id="ngs_run_annotation" name="NGS Run Annotation" version="0.1.7.2"> <description>Create a SAM format header from run metadata for sample annotation.</description> <macros> <import>toolshed_macros.xml</import> </macros> <expand macro="requirements"/> <version_command>mimodd version -q</version_command> <command> mimodd header --rg-id "$rg_id" --rg-sm "$rg_sm" #if $str($rg_cn): --rg-cn "$rg_cn" #end if #if $str($rg_ds): --rg-ds "$rg_ds" #end if #if $str($rg_date): --rg-dt "$rg_date" #end if #if $str($rg_lb): --rg-lb "$rg_lb" #end if #if $str($rg_pl): --rg-pl "$rg_pl" #end if #if $str($rg_pi): --rg-pi "$rg_pi" #end if #if $str($rg_pu): --rg-pu "$rg_pu" #end if --ofile "$outputfile" </command> <inputs> <param name="rg_id" type="text" size="80" label="read-group ID (required)"> <sanitizer invalid_char=""> <valid initial="string.printable"> <remove value=""" /> </valid> <mapping initial="none"> <add source=""" target="\""/> </mapping> </sanitizer> </param> <param name="rg_sm" type="text" size="80" label="sample name (required)"> <sanitizer invalid_char=""> <valid initial="string.printable"> <remove value=""" /> </valid> <mapping initial="none"> <add source=""" target="\""/> </mapping> </sanitizer> </param> <param name="rg_ds" type="text" size="80" label="description"> <sanitizer invalid_char=""> <valid initial="string.printable"> <remove value=""" /> </valid> <mapping initial="none"> <add source=""" target="\""/> </mapping> </sanitizer> </param> <param name="rg_date" type="text" label="date (YYYY-MM-DD) the run was produced" /> <param name="rg_cn" type="text" size="80" label="name of sequencing center"> <sanitizer invalid_char=""> <valid initial="string.printable"> <remove value=""" /> </valid> <mapping initial="none"> <add source=""" target="\""/> </mapping> </sanitizer> </param> <param name="rg_lb" type="text" size="80" label="read-group library"> <sanitizer invalid_char=""> <valid initial="string.printable"> <remove value=""" /> </valid> <mapping initial="none"> <add source=""" target="\""/> </mapping> </sanitizer> </param> <param name="rg_pl" type="text" label="platform/technology used to produce the reads" /> <param name="rg_pi" type="text" label="predicted median insert size" /> <param name="rg_pu" type="text" size="80" label="platform unit; unique identifier"> <sanitizer invalid_char=""> <valid initial="string.printable"> <remove value=""" /> </valid> <mapping initial="none"> <add source=""" target="\""/> </mapping> </sanitizer> </param> </inputs> <outputs> <data name="outputfile" format="sam" label="${rg_sm} (${rg_id}) header information from MiModd ${tool.name} on ${on_string}"/> </outputs> <help> .. class:: infomark **What it does** This tool takes the user-provided information about a next-generation sequencing run and constructs a valid header in the SAM file format from it. The result file can be used by the tools *Convert* and *Reheader* or in the *SNAP Read Alignment* step to add run metadata to sequenced reads files (or to overwrite pre-existing information). **Note:** **MiModD requires run metadata for every input file at the Alignment step !** **Tip:** While you can do Alignments from fastq file format by providing a custom header file directly to the *SNAP Read Alignment* tool, we **recommend** you to first convert all input files to and archive all datasets in SAM/BAM format with appropriate header information prior to any downstream analysis. Although a bit more time-consuming, this practice protects against information loss and ensures that the input datasets will remain useful for others in the future. </help> </tool>