Mercurial > repos > veg > bioext_bealign
diff bealign.xml @ 0:c6f0b318bc03 draft
planemo upload for repository https://github.com/davebx/bioext-gx/ commit b'43068c0d2b50c3fd9d13976dc4038950928372d1\n'-dirty
| author | veg |
|---|---|
| date | Thu, 22 Feb 2018 15:48:40 -0500 |
| parents | |
| children | 787baac95405 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/bealign.xml Thu Feb 22 15:48:40 2018 -0500 @@ -0,0 +1,128 @@ +<?xml version="1.0"?> +<tool id="bioext_bealign" name="Align sequences" version="@VERSION@.0"> + <description>to a reference using a codon alignment algorithm</description> + <macros> + <import>macros.xml</import> + </macros> + <expand macro="requirements" /> + <version_command>bealign --version</version_command> + <command detect_errors="exit_code"> + <![CDATA[ + bealign --reference $reference $advanced.expected_identity --alphabet $advanced.alphabet + --score-matrix $advanced.score_matrix $advanced.reverse_complement $advanced.keep_reference + #if $advanced.discard: + $advanced.discard $advanced.discarded_reads + #end if + $input $output + ]]> + </command> + <inputs> + <param name="input" type="data" format="fasta" label="Input reads" /> + <conditional name="select_reference"> + <param name="reference_type" type="select"> + <option value="preset">Select preset</option> + <option value="dataset">Use a history dataset</option> + </param> + <when value="preset"> + <param argument="--reference" type="select"> + <option value="HXB2_tat">HXB2 tat</option> + <option value="HXB2_gag">HXB2 gag</option> + <option value="HXB2_pol">HXB2 polymerase</option> + <option value="HXB2_int">HXB2 integrase</option> + <option value="HXB2_vif">HXB2 vif</option> + <option value="HXB2_pr">HXB2 protease</option> + <option value="HXB2_vpr">HXB2 vpr</option> + <option value="NL4-3_prrt">NL4-3 protease and reverse transcriptase</option> + <option value="HXB2_nef">HXB2 nef</option> + <option value="HXB2_env">HXB2 envelope</option> + <option value="HXB2_rt">HXB2 reverse transcriptase</option> + <option value="HXB2_prrt">HXB2 protease and reverse transcriptase</option> + <option value="HXB2_rev">HXB2 rev</option> + <option value="HXB2_vpu">HXB2 vpu</option> + </param> + </when> + <when value="dataset"> + <param argument="--reference" type="data" format="fasta" label="Reference sequences" /> + </when> + </conditional> + <section name="advanced" title="Advanced options" expanded="False"> + <param name="expected_identity" argument="--expected-identity" type="boolean" checked="False" truevalue="--expected-identity" falsevalue="" label="Discard sequences that are insufficiently identical to the reference" /> + <param argument="--alphabet" type="select" label="Alphabet to use for alignment"> + <option value="codon" selected="True">Codon</option> + <option value="dna">DNA</option> + <option value="amino">Amino acids</option> + </param> + <param name="score_matrix" argument="--score-matrix" type="select" label="Parametrize using score matrix"> + <option value="BLOSUM62" selected="True">Blocks substitution</option> + <option value="DNA65">DNA, 65% expected identity</option> + <option value="DNA70">DNA, 70% expected identity</option> + <option value="DNA88">DNA, 88% expected identity</option> + <option value="DNA80">DNA, 80% expected identity</option> + <option value="DNA95">DNA, 95% expected identity</option> + <option value="PAM200">PAM 200 substitution</option> + <option value="PAM250">PAM 250 substitution</option> + <option value="HIV_BETWEEN_F">HIV between+F</option> + </param> + <param argument="--discard" type="boolean" checked="False" truevalue="--discard" falsevalue="" label="Output discarded sequences to a separate dataset" /> + <param name="reverse_complement" argument="--reverse-complement" type="boolean" checked="False" truevalue="--reverse-complement" falsevalue="" label="Also try to align against reverse complement of reference" /> + <param name="keep_reference" argument="--keep-reference" type="boolean" checked="False" truevalue="--keep-reference" falsevalue="" label="Include reference as first sequence in aligned BAM" /> + </section> + </inputs> + <outputs> + <data name="output" format="bam"/> + <data name="discarded_reads" format="fasta"> + <filter>discard</filter> + </data> + </outputs> + <tests> + <test> + <param name="input" ftype="fasta" value="bealign-in1.fa" /> + <param name="reference_type" value="dataset" /> + <param name="score_matrix" value="HIV_BETWEEN_F" /> + <param name="reference" ftype="fasta" value="bealign-in-ref-1.fa" /> + <output name="output" file="bealign-out1.bam" /> + </test> + <test> + <param name="input" ftype="fasta" value="bealign-in2.fa" /> + <param name="reference_type" value="dataset" /> + <param name="score_matrix" value="BLOSUM62" /> + <param name="reference" ftype="fasta" value="bealign-in-ref-2.fa" /> + <output name="output" file="bealign-out2.bam" /> + </test> + </tests> + <help> + <![CDATA[ + -r REFERENCE, --reference REFERENCE + REFERENCE FASTA file or {HXB2_tat, HXB2_nef, HXB2_vpu, + HXB2_vif, HXB2_env, HXB2_vpr, HXB2_rev, HXB2_pol, + HXB2_prrt, NL4-3_prrt, HXB2_rt, HXB2_gag, HXB2_pr, + HXB2_int} + -e EXPECTED_IDENTITY, --expected-identity EXPECTED_IDENTITY + discard sequences that are insufficiently identical to + the reference + -a ALPHABET, --alphabet ALPHABET + perform an alignment using one of {amino, dna, codon} + [default=codon] + -m SCOREMATRIX, --score-matrix SCOREMATRIX + parameterize using one of {PAM250, DNA80, + HIV_BETWEEN_F, BLOSUM62, DNA70, DNA88, PAM200, DNA95, + DNA65} [default=BLOSUM62] + -D DISCARD, --discard DISCARD + discarded sequences are sent to DISCARD + -R, --reverse-complement + also align the reverse complement of each query + sequence, returning it if the alignment is superior + -S, --no-sort do NOT sort the resulting BAM file [the default is to + sort] + -q, --quiet do not print status update messages + -v, --version print version information and exit + -K, --keep-reference include the reference sequence as the first one in the + resulting BAM file [the default is to strip it] + ]]> + </help> +</tool> + + + + +
