Mercurial > repos > iuc > mothur_screen_seqs
diff screen.seqs.xml @ 1:d0190913cb6c draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/mothur commit a9d1e0debcd357d8080a1c6c5f1d206dd45a7a4d
| author | iuc |
|---|---|
| date | Fri, 19 May 2017 05:17:26 -0400 |
| parents | 5a01375eadf0 |
| children | 7dabd4117ad1 |
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--- a/screen.seqs.xml Fri Jun 24 16:49:07 2016 -0400 +++ b/screen.seqs.xml Fri May 19 05:17:26 2017 -0400 @@ -4,8 +4,11 @@ <import>macros.xml</import> </macros> <expand macro="requirements"/> + <expand macro="stdio"/> <expand macro="version_command"/> - <command detect_errors="aggressive"><![CDATA[ + <command><![CDATA[ + @SHELL_OPTIONS@ + ## create symlinks to input datasets ln -s "$fasta_in" fasta_in.dat && ln -s "$names_in" names_in.dat && @@ -19,25 +22,25 @@ echo 'screen.seqs( fasta=fasta_in.dat - #if $start > -1: + #if int($start) > -1: ,start=$start #end if - #if $end > -1: + #if int($end) > -1: ,end=$end #end if - #if $minlength > -1: + #if int($minlength) > -1: ,minlength=$minlength #end if - #if $maxlength > -1: + #if int($maxlength) > -1: ,maxlength=$maxlength #end if - #if $maxambig > -1: + #if int($maxambig) > -1: ,maxambig=$maxambig #end if - #if $maxhomop > -1: + #if int($maxhomop) > -1: ,maxhomop=$maxhomop #end if - #if $criteria > -1: + #if int($criteria) > -1: ,criteria=$criteria #end if #if $optimize: @@ -71,6 +74,7 @@ )' | sed 's/ //g' ## mothur trips over whitespace | mothur + | tee mothur.out.log ]]></command> <inputs> <param name="fasta_in" type="data" format="fasta,mothur.align" label="fasta - Fasta to screen"/> @@ -93,7 +97,7 @@ <param name="names_in" type="data" format="mothur.names" optional="true" label="name - Sequence Names to screen"/> <param name="groups_in" type="data" format="mothur.groups" optional="true" label="group - Groups to screen"/> <param name="alignreport_in" type="data" format="mothur.align.report" optional="true" label="alignreport - Align Report to screen"/> - <param name="summary" type="data" format="mothur.summary" optional="true" label="summary - allows you to enter the summary file created by summary.seqs to save processing time when screening with parameters in the summary file"/> + <param name="summary" type="data" format="mothur.summary" optional="true" label="summary file - as created by summary.seqs" help="saves processing time when screening with parameters in the summary file"/> <param name="contigsreport" type="data" format="contigs.report" optional="true" label="contigsreport - Contigs Report to screen with" help="this file is created by the make.contigs command. If you provide the contigs report file you can screen your sequences using the following parameters: minoverlap, ostart, oend and mismatches"/> <param name="taxonomy_in" type="data" format="taxonomy" optional="true" label="taxonomy - Taxonomy to screen"/> <param name="count_in" type="data" format="mothur.count_table" optional="true" label="count - a count_table" help="generated by count.seqs"/> @@ -114,27 +118,27 @@ <data name="alignreport_out" format="mothur.align.report" from_work_dir="alignreport_in*.good.dat" label="${tool.name} on ${on_string}: align.report"> <filter>alignreport_in</filter> </data> - <data name="count_out" format="count" from_work_dir="count_in*.good.dat" label="${tool.name} on ${on_string}: count"> + <data name="count_out" format="mothur.count_table" from_work_dir="count_in*.good.dat" label="${tool.name} on ${on_string}: count"> <filter>count_in</filter> </data> </outputs> <tests> <test> - <param name="fasta_in" value="Mock_S280_L001_R1_001_small.trim.contigs.fasta"/> + <param name="fasta_in" value="Mock_S280_L001_R1_001_small.trim.contigs.fasta" ftype="fasta"/> <param name="maxambig" value="0"/> <param name="maxlength" value="275"/> - <output name="fasta_out" file="Mock_S280_L001_R1_001_small.trim.contigs.good.fasta"/> - <output name="bad_accnos" file="Mock_S280_L001_R1_001_small.trim.contigs.bad.accnos"/> + <output name="fasta_out" file="Mock_S280_L001_R1_001_small.trim.contigs.good.fasta" ftype="fasta"/> + <output name="bad_accnos" file="Mock_S280_L001_R1_001_small.trim.contigs.bad.accnos" ftype="mothur.accnos"/> <expand macro="logfile-test"/> </test> <test> - <param name="fasta_in" value="amazon.fasta"/> + <param name="fasta_in" value="amazon.fasta" ftype="mothur.align"/> <param name="count_in" value="amazon.count_table"/> <param name="maxambig" value="0"/> <param name="maxlength" value="275"/> - <output name="fasta_out" md5="d41d8cd98f00b204e9800998ecf8427e"/> - <output name="count_out" md5="5f4a08bbf3ec12f954edbcc6b2a2feee"/> - <output name="bad_accnos" md5="66acde5349e34fc97be22032ce68eea5"/> + <output name="fasta_out" md5="d41d8cd98f00b204e9800998ecf8427e" ftype="mothur.align"/> + <output name="count_out" md5="5f4a08bbf3ec12f954edbcc6b2a2feee" ftype="mothur.count_table"/> + <output name="bad_accnos" md5="66acde5349e34fc97be22032ce68eea5" ftype="mothur.accnos"/> <expand macro="logfile-test"/> </test> </tests> @@ -143,14 +147,14 @@ @MOTHUR_OVERVIEW@ -**Command Documenation** +**Command Documentation** The screen.seqs_ command enables you to keep sequences that fulfill certain user defined criteria. Furthermore, it enables you to cull those sequences not meeting the criteria from a name_, group_, or align.report_ file. -.. _name: http://www.mothur.org/wiki/Name_file -.. _group: http://www.mothur.org/wiki/Group_file -.. _align.report: http://www.mothur.org/wiki/Align.seqs -.. _screen.seqs: http://www.mothur.org/wiki/Screen.seqs +.. _name: https://www.mothur.org/wiki/Name_file +.. _group: https://www.mothur.org/wiki/Group_file +.. _align.report: https://www.mothur.org/wiki/Align.seqs +.. _screen.seqs: https://www.mothur.org/wiki/Screen.seqs ]]> </help>
