annotate bwa_long/bwa_wrapper.xml @ 0:fb4844b6a98e default tip

Migrated tool version 1.0.3 from old tool shed archive to new tool shed repository

<tool id="bwa_wrapper" name="Map with BWA" version="1.0.3">
  <description></description>
  <command interpreter="python">bwa_wrapper.py 
--threads="4"
#if $genomeSource.refGenomeSource == "history":
--ref=$genomeSource.ownFile
#else:
--ref=$genomeSource.indices.value
#end if
--fastq=$paired.input1
#if $paired.sPaired == "paired":
--rfastq=$paired.input2 
#else:
--rfastq="None"
#end if
--output=$output --genAlignType=$paired.sPaired --params=$params.source_select --fileSource=$genomeSource.refGenomeSource
#if $params.source_select == "pre_set":
--maxEditDist="None" --fracMissingAligns="None" --maxGapOpens="None" --maxGapExtens="None" --disallowLongDel="None" --disallowIndel="None" --seed="None" --maxEditDistSeed="None" --mismatchPenalty="None" --gapOpenPenalty="None" --gapExtensPenalty="None" --suboptAlign="None" --noIterSearch="None" --outputTopN="None" --maxInsertSize="None" --maxOccurPairing="None"
#else:
--maxEditDist=$params.maxEditDist --fracMissingAligns=$params.fracMissingAligns --maxGapOpens=$params.maxGapOpens --maxGapExtens=$params.maxGapExtens --disallowLongDel=$params.disallowLongDel --disallowIndel=$params.disallowIndel --seed=$params.seed --maxEditDistSeed=$params.maxEditDistSeed --mismatchPenalty=$params.mismatchPenalty --gapOpenPenalty=$params.gapOpenPenalty --gapExtensPenalty=$params.gapExtensPenalty --suboptAlign=$params.suboptAlign --noIterSearch=$params.noIterSearch --outputTopN=$params.outputTopN --maxInsertSize=$params.maxInsertSize --maxOccurPairing=$params.maxOccurPairing
#end if
#if $genomeSource.refGenomeSource == "history":
--dbkey=$dbkey
#else:
--dbkey="None"
#end if
--suppressHeader=$suppressHeader
  </command>
  <inputs>
    <conditional name="genomeSource">
      <param name="refGenomeSource" type="select" label="Will you select a reference genome from your history or use a built-in index?">
        <option value="indexed">Use a built-in index</option>
        <option value="history">Use one from the history</option>
      </param>
      <when value="indexed">
        <param name="indices" type="select" label="Select a reference genome">
          <options from_file="bwa_index.loc">
            <column name="value" index="1" />
            <column name="name" index="0" />
          </options>
        </param>
      </when>
      <when value="history">
        <param name="ownFile" type="data" format="fasta" metadata_name="dbkey" label="Select a reference from history" />
      </when>
    </conditional>
    <conditional name="paired">
      <param name="sPaired" type="select" label="Is this library mate-paired?">
        <option value="single">Single-end</option>
        <option value="paired">Paired-end</option>
        <option value="longread">Long-reads</option>
      </param>
      <when value="single">
        <param name="input1" type="data" format="fastqsanger" label="FASTQ file" help="Must have Sanger-scaled quality values with ASCII offset 33"/>
      </when>
      <when value="paired">
        <param name="input1" type="data" format="fastqsanger" label="Forward FASTQ file" help="Must have Sanger-scaled quality values with ASCII offset 33"/>
        <param name="input2" type="data" format="fastqsanger" label="Reverse FASTQ file" help="Must have Sanger-scaled quality values with ASCII offset 33"/>
      </when>
      <when value="longread">
        <param name="input1" type="data" format="fastqsanger" label="FASTQ file" help="Must have Sanger-scaled quality values with ASCII offset 33"/>
      </when>
    </conditional>	
    <conditional name="params">
      <param name="source_select" type="select" label="BWA settings to use" help="For most mapping needs use Commonly Used settings. If you want full control use Full Parameter List">
        <option value="pre_set">Commonly Used</option>
        <option value="full">Full Parameter List</option>
      </param>
      <when value="pre_set" />
      <when value="full">
        <param name="maxEditDist" type="integer" value="0" label="Maximum edit distance (-n)" help="Enter this value OR a fraction of missing alignments, not both" />
        <param name="fracMissingAligns" type="float" value="0.04" label="Fraction of missing alignments given 2% uniform base error rate (-n)" help="Enter this value OR maximum edit distance, not both" />
        <param name="maxGapOpens" type="integer" value="1" label="Maximum number of gap opens (-o)" />
        <param name="maxGapExtens" type="integer" value="-1" label="Maximum number of gap extensions (-e)" help="-1 for k-difference mode (disallowing long gaps)" />
        <param name="disallowLongDel" type="integer" value="16" label="Disallow long deletion within [value] bp towards the 3'-end (-d)" />
        <param name="disallowIndel" type="integer" value="5" label="Disallow insertion/deletion within [value] bp towards the end (-i)" />
        <param name="seed" type="integer" value="-1" label="Number of first subsequences to take as seed (-l)" help="Enter -1 for infinity" />
        <param name="maxEditDistSeed" type="integer" value="2" label="Maximum edit distance in the seed (-k)" />
        <param name="mismatchPenalty" type="integer" value="3" label="Mismatch penalty (-M)" help="BWA will not search for suboptimal hits with a score lower than [value]" />
        <param name="gapOpenPenalty" type="integer" value="11" label="Gap open penalty (-O)" />
        <param name="gapExtensPenalty" type="integer" value="4" label="Gap extension penalty (-E)" />
        <param name="suboptAlign" type="boolean" truevalue="true" falsevalue="false" checked="no" label="Proceed with suboptimal alignments even if the top hit is a repeat" help="By default, BWA only searches for suboptimal alignments if the top hit is unique. Using this option has no effect on accuracy for single-end reads. It is mainly designed for improving the alignment accuracy of paired-end reads. However, the pairing procedure will be slowed down, especially for very short reads (~32bp) (-R)" />
        <param name="noIterSearch" type="boolean" truevalue="true" falsevalue="false" checked="no" label="Disable iterative search" help="All hits with no more than maxDiff differences will be found. This mode is much slower than the default (-N)" />
        <param name="outputTopN" type="integer" value="-1" label="Output top [value] hits" help="For single-end reads only. Enter -1 to disable outputting multiple hits. NOTE: If you put in a positive value here, your output will NOT be in SAM format (-n)" />
        <param name="maxInsertSize" type="integer" value="500" label="Maximum insert size for a read pair to be considered as being mapped properly" help="For paired-end reads only. Only used when there are not enough good alignments to infer the distribution of insert sizes (-a)" />
        <param name="maxOccurPairing" type="integer" value="100000" label="Maximum occurrences of a read for pairing" help="For paired-end reads only. A read with more occurrences will be treated as a single-end read. Reducing this parameter helps faster pairing (-o)" />
      </when>
    </conditional>
    <param name="suppressHeader" type="boolean" truevalue="true" falsevalue="false" checked="true" label="Suppress the header in the output SAM file" help="BWA produces SAM with several lines of header information" />
  </inputs>
  <outputs>
    <data format="sam" name="output" />
  </outputs>
  <tests>
    <test>
      <!--
      BWA commands:
      bwa aln -t 4 phiX test-data/bwa_wrapper_in1.fastq > bwa_wrapper_out1.sai
      bwa samse phiX bwa_wrapper_out1.sai test-data/bwa_wrapper_in1.fastq >> bwa_wrapper_out1.sam
      phiX.fasta is the prefix for the reference
      remove the comment lines (beginning with '@') from the resulting sam file
      note that 'phiX' should be 'PHIX174' to match what's in the indexed file 
      -->
      <param name="refGenomeSource" value="indexed" />
      <param name="indices" value="phiX" />
      <param name="sPaired" value="single" />
      <param name="input1" value="bwa_wrapper_in1.fastq" ftype="fastqsanger" />
      <param name="source_select" value="pre_set" />
      <param name="suppressHeader" value="true" />
      <output name="output" file="bwa_wrapper_out1.sam" ftype="sam" sort="true" />
    </test>
    <test>
      <!--
      BWA commands:
      cp test-data/phiX.fasta phiX.fasta
      bwa index -a is phiX.fasta
      bwa aln -n 0.04 -o 1 -e -1 -d 16 -i 5 -k 2 -t 4 -M 3 -O 11 -E 4 -R -N phiX.fasta test-data/bwa_wrapper_in1.fastq > bwa_wrapper_out2.sai
      bwa samse phiX.fasta bwa_wrapper_out2.sai test-data/bwa_wrapper_in1.fastq >> bwa_wrapper_out2.sam
      phiX.fasta is the prefix for the reference
      remove the comment lines (beginning with '@') from the resulting sam file
      -->
      <param name="refGenomeSource" value="history" />
      <param name="ownFile" value="phiX.fasta" />
      <param name="sPaired" value="single" />
      <param name="input1" value="bwa_wrapper_in1.fastq" ftype="fastqsanger" />
      <param name="source_select" value="full" />
      <param name="maxEditDist" value="0" />  
      <param name="fracMissingAligns" value="0.04" />
      <param name="maxGapOpens" value="1" />
      <param name="maxGapExtens" value="-1" />
      <param name="disallowLongDel" value="16" />
      <param name="disallowIndel" value="5" />
      <param name="seed" value="-1" />
      <param name="maxEditDistSeed" value="2" />
      <param name="mismatchPenalty" value="3" />
      <param name="gapOpenPenalty" value="11" />
      <param name="gapExtensPenalty" value="4" />
      <param name="suboptAlign" value="true" />
      <param name="noIterSearch" value="true" />
      <param name="outputTopN" value="-1" />
      <param name="maxInsertSize" value="500" />
      <param name="maxOccurPairing" value="100000" />
      <param name="suppressHeader" value="true" />
      <output name="output" file="bwa_wrapper_out2.sam" ftype="sam" sort="true" />
    </test> 
    <test>
      <!--
      BWA commands:
      bwa aln -n 0.04 -o 1 -e -1 -d 16 -i 5 -k 2 -t 4 -M 3 -O 11 -E 4 -R -N phiX.fasta test-data/bwa_wrapper_in2.fastq > bwa_wrapper_out3a.sai
      bwa aln -n 0.04 -o 1 -e -1 -d 16 -i 5 -k 2 -t 4 -M 3 -O 11 -E 4 -R -N phiX.fasta test-data/bwa_wrapper_in3.fastq > bwa_wrapper_out3b.sai
      bwa sampe -a 500 -o 100000 phiX.fasta bwa_wrapper_out3a.sai bwa_wrapper_out3b.sai test-data/bwa_wrapper_in2.fastq test-data/bwa_wrapper_in3.fastq >> bwa_wrapper_out3.sam
      phiX.fasta is the prefix for the reference
      remove the comment lines (beginning with '@') from the resulting sam file
      note that 'phiX' should be 'PHIX174' to match what's in the indexed file 
      -->
      <param name="refGenomeSource" value="indexed" />
      <param name="indices" value="phiX" />
      <param name="sPaired" value="paired" />
      <param name="input1" value="bwa_wrapper_in2.fastq" ftype="fastqsanger" />
      <param name="input2" value="bwa_wrapper_in3.fastq" ftype="fastqsanger" />
      <param name="source_select" value="full" />
      <param name="maxEditDist" value="0" />
      <param name="fracMissingAligns" value="0.04" />
      <param name="maxGapOpens" value="1" />
      <param name="maxGapExtens" value="-1" />
      <param name="disallowLongDel" value="16" />
      <param name="disallowIndel" value="5" />
      <param name="seed" value="-1" />
      <param name="maxEditDistSeed" value="2" />
      <param name="mismatchPenalty" value="3" />
      <param name="gapOpenPenalty" value="11" />
      <param name="gapExtensPenalty" value="4" />
      <param name="suboptAlign" value="true" />
      <param name="noIterSearch" value="true" />
      <param name="outputTopN" value="-1" />
      <param name="maxInsertSize" value="500" />
      <param name="maxOccurPairing" value="100000" />
      <param name="suppressHeader" value="true" />
      <output name="output" file="bwa_wrapper_out3.sam" ftype="sam" sort="true" />
    </test>
  </tests> 
  <help>

**What it does**

BWA is a fast light-weighted tool that aligns relatively short sequences (queries) to a sequence database (large), such as the human reference genome. It is developed by Heng Li at the Sanger Insitute. Li H. and Durbin R. (2009) Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics, 25, 1754-60. 

------

**Know what you are doing**

.. class:: warningmark

There is no such thing (yet) as an automated gearshift in short read mapping. It is all like stick-shift driving in San Francisco. In other words = running this tool with default parameters will probably not give you meaningful results. A way to deal with this is to **understand** the parameters by carefully reading the `documentation`__ and experimenting. Fortunately, Galaxy makes experimenting easy.

 .. __: http://bio-bwa.sourceforge.net/

------

**Input formats**

BWA accepts files in Sanger FASTQ format. Use the FASTQ Groomer to prepare your files.

------

**Outputs**

The output is in SAM format, and has the following columns::

    Column  Description
  --------  --------------------------------------------------------
  1  QNAME  Query (pair) NAME
  2  FLAG   bitwise FLAG
  3  RNAME  Reference sequence NAME
  4  POS    1-based leftmost POSition/coordinate of clipped sequence
  5  MAPQ   MAPping Quality (Phred-scaled)
  6  CIGAR  extended CIGAR string
  7  MRNM   Mate Reference sequence NaMe ('=' if same as RNAME)
  8  MPOS   1-based Mate POSition
  9  ISIZE  Inferred insert SIZE
  10 SEQ    query SEQuence on the same strand as the reference
  11 QUAL   query QUALity (ASCII-33 gives the Phred base quality)
  12 OPT    variable OPTional fields in the format TAG:VTYPE:VALU
  
The flags are as follows::

    Flag  Description
  ------  -------------------------------------
  0x0001  the read is paired in sequencing
  0x0002  the read is mapped in a proper pair
  0x0004  the query sequence itself is unmapped
  0x0008  the mate is unmapped
  0x0010  strand of the query (1 for reverse)
  0x0020  strand of the mate
  0x0040  the read is the first read in a pair
  0x0080  the read is the second read in a pair
  0x0100  the alignment is not primary

It looks like this (scroll sideways to see the entire example)::

  QNAME	FLAG	RNAME	POS	MAPQ	CIAGR	MRNM	MPOS	ISIZE	SEQ	QUAL	OPT
  HWI-EAS91_1_30788AAXX:1:1:1761:343	4	*	0	0	*	*	0	0	AAAAAAANNAAAAAAAAAAAAAAAAAAAAAAAAAAACNNANNGAGTNGNNNNNNNGCTTCCCACAGNNCTGG	hhhhhhh;;hhhhhhhhhhh^hOhhhhghhhfhhhgh;;h;;hhhh;h;;;;;;;hhhhhhghhhh;;Phhh
  HWI-EAS91_1_30788AAXX:1:1:1578:331	4	*	0	0	*	*	0	0	GTATAGANNAATAAGAAAAAAAAAAATGAAGACTTTCNNANNTCTGNANNNNNNNTCTTTTTTCAGNNGTAG	hhhhhhh;;hhhhhhhhhhhhhhhhhhhhhhhhhhhh;;h;;hhhh;h;;;;;;;hhhhhhhhhhh;;hhVh

-------

**BWA settings**

All of the options have a default value. You can change any of them. All of the options in BWA have been implemented here.

------

**BWA parameter list**

This is an exhaustive list of BWA options:

For **aln**::

  -n NUM  Maximum edit distance if the value is INT, or the fraction of missing
          alignments given 2% uniform base error rate if FLOAT. In the latter
          case, the maximum edit distance is automatically chosen for different 
          read lengths. [0.04]
  -o INT  Maximum number of gap opens [1]
  -e INT  Maximum number of gap extensions, -1 for k-difference mode
          (disallowing long gaps) [-1]
  -d INT  Disallow a long deletion within INT bp towards the 3'-end [16]
  -i INT  Disallow an indel within INT bp towards the ends [5]
  -l INT  Take the first INT subsequence as seed. If INT is larger than the
          query sequence, seeding will be disabled. For long reads, this option 
          is typically ranged from 25 to 35 for '-k 2'. [inf]
  -k INT  Maximum edit distance in the seed [2]
  -t INT  Number of threads (multi-threading mode) [1]
  -M INT  Mismatch penalty. BWA will not search for suboptimal hits with a score
          lower than (bestScore-misMsc). [3]
  -O INT  Gap open penalty [11]
  -E INT  Gap extension penalty [4]
  -c      Reverse query but not complement it, which is required for alignment
          in the color space.
  -R      Proceed with suboptimal alignments even if the top hit is a repeat. By
          default, BWA only searches for suboptimal alignments if the top hit is
          unique. Using this option has no effect on accuracy for single-end
          reads. It is mainly designed for improving the alignment accuracy of
          paired-end reads. However, the pairing procedure will be slowed down,
          especially for very short reads (~32bp).
  -N      Disable iterative search. All hits with no more than maxDiff
          differences will be found. This mode is much slower than the default.

For **samse**::

  -n INT  Output up to INT top hits. Value -1 to disable outputting multiple
          hits. NOTE: Entering a value other than -1 will result in output that
          is not in SAM format, and therefore not usable further down the
          pipeline. Check the BWA documentation for details on the format of
          the output. [-1]

For **sampe**::

  -a INT  Maximum insert size for a read pair to be considered as being mapped
          properly. Since version 0.4.5, this option is only used when there
          are not enough good alignment to infer the distribution of insert
          sizes. [500]
  -o INT  Maximum occurrences of a read for pairing. A read with more
          occurrences will be treated as a single-end read. Reducing this
          parameter helps faster pairing. [100000]

  </help>
  <code file="bwa_wrapper_code.py" />
</tool>