Mercurial > repos > iuc > mothur_trim_seqs
diff trim.seqs.xml @ 5:4929eb3e0037 draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/mothur commit 38a2bbee32eaaceeb22d7549b13dbc0c613ee173
| author | iuc |
|---|---|
| date | Tue, 20 Mar 2018 13:33:54 -0400 |
| parents | e695fda56931 |
| children |
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--- a/trim.seqs.xml Wed Feb 14 11:44:21 2018 -0500 +++ b/trim.seqs.xml Tue Mar 20 13:33:54 2018 -0400 @@ -114,6 +114,7 @@ <param name="count" type="data" format="mothur.count_table" optional="true" label="count - a count_table" help="The count file is similar to the name file in that it is used to represent the number of duplicate sequences for a given representative sequence. If you run trim.seqs with an oligos file that contains group labels, trim.seqs will create a new *.trim.count_table with the group information included. "/> <param name="logtransform" type="boolean" truevalue="true" falsevalue="false" checked="false" label="logtransform" help="allows you to indicate you want the averages for the qwindowaverage, rollaverage and qaverage to be calculated using a logtransform."/> <param name="checkorient" type="boolean" truevalue="true" falsevalue="false" checked="false" label="checkorient - search the reverse complement?" help="If you are running the trim.seqs command with paired barcodes or primers, you can use the checkorient parameter. When checkorient=t and mothur can't find the barcodes and primers, it will search the reverse compliment. "/> + <expand macro="param-savelog"/> </inputs> <outputs> <expand macro="logfile-output"/> @@ -158,6 +159,7 @@ <output name="scrap_fasta" md5="4f791b7684662f1f962970af46429e24" ftype="fasta"/> <output name="trim_names" md5="1b8c6c47052bb69524ef56ebb764fb8f" ftype="mothur.names"/> <output name="scrap_names" md5="80f9252837e4b189f06ec00469b88e85" ftype="mothur.names"/> + <param name="savelog" value="true"/> <expand macro="logfile-test"/> </test> <test><!-- test with count table --> @@ -168,6 +170,7 @@ <output name="scrap_fasta" md5="4f791b7684662f1f962970af46429e24" ftype="fasta"/> <output name="trim_count" md5="836b4d72a8cda3741ef435741783b384" ftype="mothur.count_table"/> <output name="scrap_count" md5="04ae9f50c1b6f0d8d7e1ac28f845dd4c" ftype="mothur.count_table"/> + <param name="savelog" value="true"/> <expand macro="logfile-test"/> </test> <test><!-- test with oligos --> @@ -179,6 +182,7 @@ <output name="trim_fasta" md5="75a8a3ae2d1fe1ff2b860480b84e9bd6" ftype="fasta"/> <output name="scrap_fasta" md5="c4fd14e70ab7d1c21d238e87624829d7" ftype="fasta"/> <output name="groups_file" md5="198957282c234e825414e175d926046a" ftype="mothur.groups"/> + <param name="savelog" value="true"/> <expand macro="logfile-test"/> </test> <test><!-- test with oligos and allfiles parameter --> @@ -196,6 +200,7 @@ <output_collection name="fasta_allfiles" count="9"> <element name="F003D144" md5="025ff271ac24ecb898863d7fcbfabf10" ftype="fasta"/> </output_collection> + <param name="savelog" value="true"/> <expand macro="logfile-test"/> </test> <test><!-- test with qfile--> @@ -207,6 +212,7 @@ <output name="scrap_fasta" md5="a4d3ef3d91b4c0146ec84bb7aad3987c" ftype="fasta"/> <output name="trim_qual" md5="3d4e2d3c7dd43b90660ab9c923d9eab1" ftype="qual454"/> <output name="scrap_qual" md5="22931236d082c2b77811bbf912c1f4b1" ftype="qual454"/> + <param name="savelog" value="true"/> <expand macro="logfile-test"/> </test> </tests>
