Mercurial > repos > saskia-hiltemann > cgatools_v17
diff tools/cgatools17/fasta2crr.xml @ 1:3a2e0f376f26 draft
Minor change to tv2vcf.xml to allow for workflow automation
author | dgdekoning |
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date | Wed, 21 Oct 2015 10:09:15 -0400 |
parents | |
children | 91e163b708d3 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/tools/cgatools17/fasta2crr.xml Wed Oct 21 10:09:15 2015 -0400 @@ -0,0 +1,70 @@ +<tool id="fasta2crr" name="fasta-2-crr" version="1.7.1"> + <description> Convert fasta sequences into a single reference crr file </description> + + <requirements> + <requirement type="package" version="1">cgatools17</requirement> + </requirements> + + <command> + cgatools | head -1; + cgatools fasta2crr + #for $f in $fastafiles + --input ${f.file} + #end for + --output $output + #if $circ != "None" + --circular $circ + #end if + </command> + + <inputs> + <repeat name="fastafiles" title="FASTA File" min="1"> + <param name="file" type="data" format="tsv" label="select input fasta file" /> + </repeat> + <param name="circ" type="data" format="tsv,bz2" optional="true" label="select file containing comma-separated list of circular chromosome names"/> + <param name="fname" type="text" value="" label="Prefix for your output file" help="Optional"/> + </inputs> + + <outputs> + <data format="crr" name="output" label="$fname ${tool.name} on ${on_string}"/> + </outputs> + + <help> + +**What it does** + +This tool converts input FASTA sequences into a single reference CRR file. + +**cgatools 1.7.1 Documentation** + +Userguide: http://cgatools.sourceforge.net/docs/1.7.1/cgatools-user-guide.pdf + +Release notes: http://cgatools.sourceforge.net/docs/1.7.1/cgatools-release-notes.pdf + +**Command line reference**:: + + COMMAND NAME + fasta2crr - Converts fasta reference files to the crr format. + + OPTIONS + -h [ --help ] + Print this help message. + + --input arg + The input fasta files (may be passed in as arguments at the end of the + command, or omitted for stdin). Take care to specify the fasta files in + chromosome order; ordering is important. To work with human Complete + Genomics data, the chromosome order should be chr1...chr22, chrX, chrY, + chrM. + + --output arg + The output crr file. + + --circular arg + A comma-separated list of circular chromosome names. If ommitted, + defaults to chrM. + + </help> +</tool> + +