Mercurial > repos > edward-kirton > lucy
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Migrated tool version 1.0.1 from old tool shed archive to new tool shed repository
author | edward-kirton |
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date | Tue, 07 Jun 2011 17:27:29 -0400 |
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<tool id="lucy" name="LUCY trimmer" version='1.0.1' description="Less Useful Chunks Yank"> <command interpreter='perl'>psub -l galaxy_normal.c --fasta $fasta_infile --cat $fasta_outfile --cat $qual_outfile lucy -quiet -xtra 8 -error $max_avg_error $max_error_at_ends -bracket $bracket_window_size $bracket_max_avg_error #if $vector.vector_select == '1': -vector $vector.vector_fasta_infile $vector.splice_fasta_infile #end if -output $fasta_outfile $qual_outfile $fasta_infile $qual_infile </command> <inputs> <param name="fasta_infile" type="data" format="fasta" label="Read sequences (Fasta)"/> <param name="qual_infile" type="data" format="qual454" label="Qual scores input file (qual454)"/> <param name="max_avg_error" type="text" value='.007' label="max average error"/> <param name="max_error_at_ends" type="text" value='.007' label="max error at ends"/> <param name="bracket_window_size" type="integer" value='20' label="bracket window size"/> <param name="bracket_max_avg_error" type="text" value='.007' label="bracket max average error"/> <conditional name='vector'> <param name="vector_select" type="select" label="Do you have vector sequence files?" > <option value="0">no, just trim by quality alone</option> <option value="1">yes</option> </param> <when value='1'> <param name="vector_fasta_infile" type="data" format="fasta" label="Complete cloning vector sequence (Fasta)"/> <param name="splice_fasta_infile" type="data" format="fasta" label="Subsequence before and after each insert site (Fasta)"/> </when> <when value='0'> </when> </conditional> </inputs> <outputs> <data name="fasta_outfile" format="fasta"/> <data name="qual_outfile" format="qual454"/> </outputs> <help> Less Useful Chunks Yank (lucy) is a utility that prepares raw DNA sequence fragments for sequence assembly. It performs quality end-trimming and optionally removal of primer/vector sequences or filtering contamination. --- Each sequence in the output sequence file begins with a header that includes its name, three pass along clone length values to the fragment assembly program, and a left and right marker denoting the begin and end of the good quality, vector free region. The following is an example of lucy output:: >GCCAA03TF 1500 3000 2000 43 490 AGCCAAGTTTGCAGCCCTGCAGGTCGACTCTAGAGGATCCCCAGGATGATCAGCCACATT GGGACTGAGACACGGCCCAAACTCCTACGGGAGGCAGCAGTGGGGAATCTTGCGCAATGG GCGAAAGCCTGACGCAGCCATGCCGCGTGAATGATGAAGGTCTTAGGATTGTAAAATTCT TTCACCGGGGACGATAATGACGGTACCCGGAGAAGAAGCCCCGGCTAACTTCGTGCCAGC ... --- **Manual** http://galaxy.jgi-psf.org/static/manuals/lucy.pdf </help> </tool>