view nhmmscan.xml.orig @ 11:405dd85a9408 draft default tip

"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/hmmer3 commit e0d4688a59e6eeba33adcfe803ac43d0bc2863e7"

<?xml version="1.0"?>
<<<<<<< HEAD
<tool id="hmmer_nhmmscan" name="nhmmscan" version="@TOOL_VERSION@+galaxy1">
  <description>search DNA sequence(s) against a DNA profile database</description>
  <macros>
    <import>macros.xml</import>
  </macros>
  <expand macro="requirements"/>
  <expand macro="stdio"/>
  <command><![CDATA[
@ADDTHREADS@
=======
<tool id="hmmer_nhmmscan" name="nhmmscan" version="@TOOL_VERSION@">
    <description>search DNA sequence(s) against a DNA profile database</description>
    <expand macro="bio_tools"/>
    <macros>
        <import>macros.xml</import>
    </macros>
    <expand macro="requirements"/>
    <expand macro="stdio"/>
    <command><![CDATA[
>>>>>>> c37d72558 (add more bio.tool IDs)
@INPUTHMMCHOICE@
nhmmscan

@OFORMAT_WITH_OPTS@
@THRESHOLDS_NODOM@
@CUT@
@ACCEL_HEUR@
--B1 $B1
--B2 $B2
--B3 $B3

@ADV_OPTS@
@LENGTHS@
@CPU@
@SEED@

'$input_hmm_filename'
'$seqfile'
> '$output'
  ]]></command>
  <inputs>
    <expand macro="input_hmm_choice" />
    <!-- todo use Galaxy features like data libraries/data tables/??? -->
    <param name="seqfile" type="data" format="fasta" label="Sequence file"/>
    <expand macro="oformat_with_opts_dfam_alisc"/>
    <expand macro="thresholds_nodom"/>
    <expand macro="cut"/>
    <expand macro="accel_heur_xml"/>

    <param argument="--B1" type="integer" value="110" label="window length for biased-composition modifier (MSV)" />
    <param argument="--B2" type="integer" value="240" label="window length for biased-composition modifier (Vit)" />
    <param argument="--B3" type="integer" value="1000" label="window length for biased-composition modifier (Fwd)" />

    <expand macro="adv_opts"/>
    <expand macro="lengths"/>
    <expand macro="seed"/>
  </inputs>
  <outputs>
    <expand macro="output_dfam_alisc" tool="NHMMSCAN"/>
  </outputs>
  <tests>
    <test expect_num_outputs="3">
      <param name="input_hmm_conditional|input_hmm_source" value="history"/>
      <param name="input_hmm_conditional|hmmfile" value="MADE1.hmm"/>
      <param name="seqfile" value="dna_target.fa"/>
      <expand macro="oformat_test" />
      <expand macro="seed_test" />
      <output name="output" file="MADE1.nhmmscan_out" lines_diff="12">
          <expand macro="assert_out" tool="nhmmscan"/>
      </output>
      <output name="tblout" file="MADE1.nhmmscan_out.tblout" lines_diff="10">
          <!-- nhmmscan reports as hmmscan https://github.com/EddyRivasLab/hmmer/issues/190 -->
          <expand macro="assert_tblout" tool="hmmscan"/>
      </output>
      <output name="dfamtblout" file="MADE1.nhmmscan_out.dfamtblout">
          <assert_contents>
              <has_line_matching expression="# hit scores"/>
          </assert_contents>
      </output>
      <!--not test because https://github.com/EddyRivasLab/hmmer/issues/190 <output name="aliscoresout" file="MADE1.nhmmscan_out.aliscoresout" lines_diff="10" />-->
    </test>
  </tests>
  <help><![CDATA[
@HELP_PRE@

nhmmscan is used to search nucleotide sequences against collections of
nucleotide profiles. For each sequence in <seqfile>, use that query sequence to
search the target database of profiles in <hmmfile>, and output ranked lists of
the profiles with the most significant matches to the sequence.

The <seqfile> may contain more than one query sequence. It can be in FASTA
format, or several other common sequence file formats (genbank, embl, and
uniprot, among others), or in alignment file formats (stockholm, aligned fasta,
and others). See the --qformat option for a complete list.

@HELP_PRE_OTH@

@OFORMAT_WITH_OPTS_N_HELP@
@THRESHOLDS_NODOM_HELP@
@CUT_HELP@
@ACCEL_HEUR_HELP@
@BIAS_COMP_HELP@
@ADV_OPTS_HELP@
@LENGTHS_HELP@
@SEED_HELP@


@ATTRIBUTION@
]]></help>
  <expand macro="citation"/>
</tool>