view sam_header.xml @ 24:3accdbe6503b draft default tip

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<tool id="ngs_run_annotation" name="NGS Run Annotation" version="0.1.7.3">
  <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>python3 -m MiModD version -q</version_command>
  <command>
  	python3 -m 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 label="read-group ID (required)" name="rg_id" size="80" type="text">
        <sanitizer invalid_char="">
            <valid initial="string.printable">
                <remove value="&quot;" />
            </valid>
            <mapping initial="none">
                <add source="&quot;" target="\&quot;" />
            </mapping>
        </sanitizer>
    </param>
    <param label="sample name (required)" name="rg_sm" size="80" type="text">
        <sanitizer invalid_char="">
            <valid initial="string.printable">
                <remove value="&quot;" />
            </valid>
            <mapping initial="none">
                <add source="&quot;" target="\&quot;" />
            </mapping>
        </sanitizer>
    </param>
    <param label="description" name="rg_ds" size="80" type="text">
        <sanitizer invalid_char="">
            <valid initial="string.printable">
                <remove value="&quot;" />
            </valid>
            <mapping initial="none">
                <add source="&quot;" target="\&quot;" />
            </mapping>
        </sanitizer>
    </param>
    <param label="date (YYYY-MM-DD) the run was produced" name="rg_date" type="text" />
    <param label="name of sequencing center" name="rg_cn" size="80" type="text">
        <sanitizer invalid_char="">
            <valid initial="string.printable">
                <remove value="&quot;" />
            </valid>
            <mapping initial="none">
                <add source="&quot;" target="\&quot;" />
            </mapping>
        </sanitizer>
    </param>
    <param label="read-group library" name="rg_lb" size="80" type="text">
        <sanitizer invalid_char="">
            <valid initial="string.printable">
                <remove value="&quot;" />
            </valid>
            <mapping initial="none">
                <add source="&quot;" target="\&quot;" />
            </mapping>
        </sanitizer>
    </param>
    <param label="platform/technology used to produce the reads" name="rg_pl" type="text" />
    <param label="predicted median insert size" name="rg_pi" type="text" />
    <param label="platform unit; unique identifier" name="rg_pu" size="80" type="text">
        <sanitizer invalid_char="">
            <valid initial="string.printable">
                <remove value="&quot;" />
            </valid>
            <mapping initial="none">
                <add source="&quot;" target="\&quot;" />
            </mapping>
        </sanitizer>
    </param>
  </inputs>

  <outputs>
    <data format="sam" label="${rg_sm} (${rg_id}) header information from MiModd ${tool.name} on ${on_string}" name="outputfile" />
  </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>