Mercurial > repos > xuebing > sharplabtool
diff tools/fasta_tools/fasta_concatenate_by_species.xml @ 0:9071e359b9a3
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author | xuebing |
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date | Fri, 09 Mar 2012 19:37:19 -0500 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/tools/fasta_tools/fasta_concatenate_by_species.xml Fri Mar 09 19:37:19 2012 -0500 @@ -0,0 +1,72 @@ +<tool id="fasta_concatenate0" name="Concatenate" version="0.0.0"> + <description>FASTA alignment by species</description> + <command interpreter="python">fasta_concatenate_by_species.py $input1 $out_file1</command> + <inputs> + <param name="input1" type="data" format="fasta" label="FASTA alignment"/> + </inputs> + <outputs> + <data name="out_file1" format="fasta"/> + </outputs> + <tests> + <test> + <param name="input1" value="cf_maf2fasta.dat" /> + <output name="out_file1" file="fasta_concatenate_out.fasta" /> + </test> + </tests> + <help> + +**What it does** + +This tools attempts to parse FASTA headers to determine the species for each sequence in a multiple FASTA alignment. +It then linearly concatenates the sequences for each species in the file, creating one sequence per determined species. + +------- + +**Example** + +Starting FASTA:: + + >hg18.chr1(+):10016339-10016341|hg18_0 + GT + >panTro2.chr1(+):10195380-10195382|panTro2_0 + GT + >rheMac2.chr1(+):13119747-13119749|rheMac2_0 + GT + >mm8.chr4(-):148269679-148269681|mm8_0 + GT + >canFam2.chr5(+):66213635-66213637|canFam2_0 + GT + + >hg18.chr1(-):100323677-100323679|hg18_1 + GT + >panTro2.chr1(-):101678671-101678673|panTro2_1 + GT + >rheMac2.chr1(-):103154011-103154013|rheMac2_1 + GT + >mm8.chr3(+):116620616-116620618|mm8_1 + GT + >canFam2.chr6(+):52954092-52954094|canFam2_1 + GT + + + +becomes:: + + >hg18 + GTGT + >panTro2 + GTGT + >rheMac2 + GTGT + >mm8 + GTGT + >canFam2 + GTGT + + +.. class:: warningmark + + This tool will only work properly on files with Galaxy style FASTA headers. + +</help> +</tool> \ No newline at end of file