view picard_SamToFastq.xml @ 31:585027e65f3b draft

planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/picard commit 70d2a66c405be58d4413753792bcadf212a4da84

<tool name="SamToFastq" id="picard_SamToFastq" version="@TOOL_VERSION@.@WRAPPER_VERSION@">
    <description>extract reads and qualities from SAM/BAM dataset and convert to fastq</description>
    <macros>
        <import>picard_macros.xml</import>
        <token name="@WRAPPER_VERSION@">3</token>
    </macros>
    <xrefs>
        <xref type="bio.tools">picard_samtofastq</xref>
    </xrefs>
    <expand macro="requirements" />
    <command detect_errors="exit_code"><![CDATA[

    @java_options@
    @symlink_element_identifier@

    picard
    SamToFastq

    INPUT='$escaped_element_identifier'

    #if str($single_or_paired) == "pe_interleaved":
      FASTQ='${interleaved_fastq}'
      INTERLEAVE=TRUE
    #else if str($single_or_paired) == "pe_sep":
      F='${fq1}'
      F2='${fq2}'
      FU='${fq_u}'
    #else
      F='${fq_single}'
    #end if

    RE_REVERSE="${re_reverse}"

    INCLUDE_NON_PF_READS="${include_non_pf_reads}"
    #if len(str($clipping_attribute)) > 0:
       CLIPPING_ATTRIBUTE="${clipping_attribute}"
    #end if
    #if len(str($clipping_action)) > 0:
       CLIPPING_ACTION="${clipping_action}"
    #end if
    READ1_TRIM="${read1_trim}"

    #if int($read1_max_bases_to_write) > -1:
      READ1_MAX_BASES_TO_WRITE="${read1_max_bases_to_write}"
    #end if

    READ2_TRIM="${read2_trim}"

    #if int($read2_max_bases_to_write) > -1:
      READ2_MAX_BASES_TO_WRITE="${read2_max_bases_to_write}"
    #end if

    INCLUDE_NON_PRIMARY_ALIGNMENTS="${include_non_primary_alignments}"

    VALIDATION_STRINGENCY="${validation_stringency}"
    QUIET=true
    VERBOSITY=ERROR
    @TMPDIR_OPTION@

  ]]></command>
  <inputs>

    <param format="sam,bam" name="inputFile" type="data" label="Select SAM/BAM dataset or dataset collection" help="If empty, upload or import a SAM/BAM dataset"/>
    <param name="single_or_paired" type="select" label="Output format">
        <option value="se" >Single-end</option>
        <option value="pe_interleaved" selected="true">Paired-end (one interleaved output file)</option>
        <option value="pe_sep">Paired-end (two separate output files)</option>
    </param>

    <param name="re_reverse" type="boolean" checked="True" label="Re-reverse bases and qualities of reads with negative strand flag set before writing them to fastq" help="RE_REVERSE; default=True"/>
    <param name="include_non_pf_reads" type="boolean" label="Include non-PF reads from the SAM/BAM dataset into the output FASTQ" help="INCLUDE_NON_PF_READS; PF means 'passes filtering'. Reads whose 'not passing quality controls' flag is set are non-PF reads; default=False"/>
    <param name="clipping_attribute" type="text" value="" label="The attribute that stores the position at which the SAM/BAM record should be clipped" help="CLIPPING_ATTRIBUTE; default=null"/>
    <param name="clipping_action" type="text" value="" label="The action that should be taken with clipped reads: 'X' means the reads and qualities should be trimmed at the clipped position; 'N' means the bases should be changed to Ns in the clipped region; and any integer means that the base qualities should be set to that value in the clipped region" help="CLIPPING_ACTION; default=null"/>
    <param name="read1_trim" type="integer" value="0" min="0" label="The number of bases to trim from the beginning of read 1" help="READ1_TRIM; default=0"/>
    <param name="read1_max_bases_to_write" type="integer" value="-1" label="The maximum number of bases to write from read 1 after trimming" help="READ1_MAX_BASES_TO_WRITE; If there are fewer than this many bases left after trimming, all will be written. If this value is null then all bases left after trimming will be written; default=null (-1)"/>
    <param name="read2_trim" type="integer" value="0" min="0" label="The number of bases to trim from the beginning of read 2" help="READ2_TRIM; default=0"/>
    <param name="read2_max_bases_to_write" type="integer" value="-1" label="The maximum number of bases to write from read 2 after trimming" help="READ2_MAX_BASES_TO_WRITE; If there are fewer than this many bases left after trimming, all will be written. If this value is null then all bases left after trimming will be written; default=null (-1)"/>
    <param name="include_non_primary_alignments" type="boolean" label="If true, include non-primary alignments in the output" help="INCLUDE_NON_PRIMARY_ALIGNMENTS; Support of non-primary alignments in SamToFastq is not comprehensive, so there may be exceptions if this is set to true and there are paired reads with non-primary alignments; default=False"/>

    <expand macro="VS" />

  </inputs>

  <outputs>
    <data format="fastqsanger" name="fq_single" label="${tool.name} on ${on_string}: reads as fastq">
        <filter>output_type['single_or_paired'] == 'se'</filter>
    </data>

    <data format="fastqsanger" name="interleaved_fastq" label="Interleaved pairs from ${tool.name} on ${on_string}">
        <filter>output_type['single_or_paired'] == 'pe_interleaved'</filter>
    </data>

    <data format="fastqsanger" name="fq1" label="Paired-end forward strand from ${tool.name} on ${on_string}">
        <filter>output_type['single_or_paired'] == 'pe_sep'</filter>
    </data>

    <data format="fastqsanger" name="fq2" label="Paired-end reverse strand from ${tool.name} on ${on_string}">
        <filter>output_type['single_or_paired'] == 'pe_sep'</filter>
    </data>

    <data format="fastqsanger" name="fq_u" label="Paired-end unpaired reads from ${tool.name} on ${on_string}">
        <filter>output_type['single_or_paired'] == 'pe_sep'</filter>
    </data>
  </outputs>

  <tests>
    <test>
      <param name="inputFile" value="picard_SamToFastq.bam" ftype="bam"/>
      <param name="single_or_paired" value="pe_interleaved" />
      <param name="re_reverse" value="true"/>
      <param name="include_non_pf_reads" value="false"/>
      <param name="clipping_attribute" value="" />
      <param name="clipping_action" value="" />
      <param name="read1_trim" value="0" />
      <param name="read1_max_bases_to_write" value="-1"/>
      <param name="read2_trim" value="0" />
      <param name="read2_max_bases_to_write" value="-1"/>
      <param name="include_non_primary_alignments" value="false"/>
      <output name="interleaved_fastq" file="picard_SamToFastq_test1.fq" ftype="fastqsanger"/>
    </test>
    <test>
      <param name="inputFile" value="picard_SamToFastq.bam" ftype="bam"/>
      <param name="single_or_paired" value="pe_sep" />
      <param name="re_reverse" value="true"/>
      <param name="include_non_pf_reads" value="false"/>
      <param name="clipping_attribute" value="" />
      <param name="clipping_action" value="" />
      <param name="read1_trim" value="0" />
      <param name="read1_max_bases_to_write" value="-1"/>
      <param name="read2_trim" value="0" />
      <param name="read2_max_bases_to_write" value="-1"/>
      <param name="include_non_primary_alignments" value="false"/>
      <output name="fq1" file="picard_SamToFastq_1.fq" ftype="fastqsanger"/>
      <output name="fq2" file="picard_SamToFastq_2.fq" ftype="fastqsanger"/>
      <output name="fq_u" file="picard_SamToFastq_u.fq" ftype="fastqsanger"/>
    </test>
    <test>
      <param name="inputFile" value="picard_SamToFastq_se.bam" ftype="bam"/>
      <param name="single_or_paired" value="se" />
      <param name="re_reverse" value="true"/>
      <param name="include_non_pf_reads" value="false"/>
      <param name="clipping_attribute" value="" />
      <param name="clipping_action" value="" />
      <param name="read1_trim" value="0" />
      <param name="read1_max_bases_to_write" value="-1"/>
      <param name="read2_trim" value="0" />
      <param name="read2_max_bases_to_write" value="-1"/>
      <param name="include_non_primary_alignments" value="false"/>
      <output name="fq_single" file="picard_SamToFastq_se.fq" ftype="fastqsanger"/>
    </test>
  </tests>


  <help>

**Purpose**

Extracts read sequences and qualities from the input SAM/BAM dataset and outputs them in Sanger fastq format. In the RE_REVERSE=True mode (default behavior), if the read is aligned and the alignment is to the reverse strand on the genome, the read's sequence from input SAM.BAM dataset will be reverse-complemented prior to writing it to fastq in order restore correctly the original read sequence as it was generated by the sequencer.

-----

.. class:: warningmark

@dataset_collections@

@description@

  FASTQ=File
  F=File                        Output fastq file (single-end fastq or, if paired, first end of the pair fastq).
                                Required.

  SECOND_END_FASTQ=File
  F2=File                       Output fastq file (if paired, second end of the pair fastq).  Default value: null.
                                

  UNPAIRED_FASTQ=File
  FU=File                       Output fastq file for unpaired reads; may only be provided in paired-fastq mode  Default
                                value: null.

  RE_REVERSE=Boolean
  RC=Boolean                    Re-reverse bases and qualities of reads with negative strand flag set before writing them
                                to fastq  Default value: true. Possible values: {true, false}

  INTERLEAVE=Boolean
  INTER=Boolean                 Will generate an interleaved fastq if paired, each line will have /1 or /2 to describe
                                which end it came from  Default value: false. Possible values: {true, false}

  INCLUDE_NON_PF_READS=Boolean
  NON_PF=Boolean                Include non-PF reads from the SAM file into the output FASTQ files. PF means 'passes
                                filtering'. Reads whose 'not passing quality controls' flag is set are non-PF reads.
                                Default value: false. Possible values: {true, false}

  CLIPPING_ATTRIBUTE=String
  CLIP_ATTR=String              The attribute that stores the position at which the SAM record should be clipped  Default
                                value: null.

  CLIPPING_ACTION=String
  CLIP_ACT=String               The action that should be taken with clipped reads: 'X' means the reads and qualities
                                should be trimmed at the clipped position; 'N' means the bases should be changed to Ns in
                                the clipped region; and any integer means that the base qualities should be set to that
                                value in the clipped region.  Default value: null.

  READ1_TRIM=Integer
  R1_TRIM=Integer               The number of bases to trim from the beginning of read 1.  Default value: 0.

  READ1_MAX_BASES_TO_WRITE=Integer
  R1_MAX_BASES=Integer          The maximum number of bases to write from read 1 after trimming. If there are fewer than
                                this many bases left after trimming, all will be written.  If this value is null then all
                                bases left after trimming will be written.  Default value: null.

  READ2_TRIM=Integer
  R2_TRIM=Integer               The number of bases to trim from the beginning of read 2.  Default value: 0.

  READ2_MAX_BASES_TO_WRITE=Integer
  R2_MAX_BASES=Integer          The maximum number of bases to write from read 2 after trimming. If there are fewer than
                                this many bases left after trimming, all will be written.  If this value is null then all
                                bases left after trimming will be written.  Default value: null.

  INCLUDE_NON_PRIMARY_ALIGNMENTS=Boolean
                                If true, include non-primary alignments in the output.  Support of non-primary alignments
                                in SamToFastq is not comprehensive, so there may be exceptions if this is set to true and
                                there are paired reads with non-primary alignments.  Default value: false.
                                Possible values: {true, false}

@more_info@

  </help>
  <expand macro="citations" />
</tool>