Mercurial > repos > wolma > mimodd_ngs_run_annotation
view sam_header.xml @ 1:4090ff909f47 draft default tip
Uploaded
author | wolma |
---|---|
date | Fri, 16 Jan 2015 11:15:01 -0500 |
parents | 37e44e7e2d50 |
children |
line wrap: on
line source
<tool id="ngs_run_annotation" name="NGS Run Annotation"> <description>Create a SAM format header from run metadata for sample annotation.</description> <requirements> <requirement type="package" version="0.1.5">mimodd</requirement> </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>