Mercurial > repos > iuc > mothur_get_seqs
view get.seqs.xml @ 6:8b8c7cf6738c draft
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/mothur commit debdcdbb89f9bf3e2c3eed05cb078eddb27d4684"
author | iuc |
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date | Mon, 02 Dec 2019 06:26:02 -0500 |
parents | 5acd4d7339b9 |
children | c8b640a7aea1 |
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<tool profile="16.07" id="mothur_get_seqs" name="Get.seqs" version="@WRAPPER_VERSION@.0"> <description>Picks sequences by name</description> <macros> <import>macros.xml</import> </macros> <expand macro="requirements"/> <expand macro="stdio"/> <expand macro="version_command"/> <command><![CDATA[ @SHELL_OPTIONS@ ## create symlinks to input datasets ln -s '$accnos' accnos.dat && ln -s '$fasta_in' fasta_in.dat && ln -s '$fastq_in' fastq_in.dat && ln -s '$count_in' count_in.dat && ln -s '$qfile_in' qfile_in.dat && ln -s '$name_in' name_in.dat && ln -s '$group_in' group_in.dat && ln -s '$alignreport_in' alignreport_in.dat && ln -s '$list_in' list_in.dat && ln -s '$taxonomy_in' taxonomy_in.dat && echo 'get.seqs( accnos=accnos.dat, #if $fasta_in: fasta=fasta_in.dat, #end if #if $fastq_in: fastq=fastq_in.dat, #end if #if $count_in: count=count_in.dat, #end if #if $qfile_in: qfile=qfile_in.dat, #end if #if $name_in: name=name_in.dat, #end if #if $group_in: group=group_in.dat, #end if #if $alignreport_in: alignreport=alignreport_in.dat, #end if #if $list_in: list=list_in.dat, #end if #if $taxonomy_in: taxonomy=taxonomy_in.dat, #end if dups=$dups )' | sed 's/ //g' ## mothur trips over whitespace | mothur | tee mothur.out.log ]]></command> <inputs> <param name="accnos" type="data" format="mothur.accnos" label="accnos - Accession Names"/> <param name="fasta_in" type="data" format="fasta" optional="true" label="fasta - Fasta Sequences"/> <param name="qfile_in" type="data" format="qual" optional="true" label="qfile - Fasta Quality"/> <param name="fastq_in" type="data" format="fastq" optional="true" label="count - a count_table" help="fastq - allows you to select sequences from your fastq file"/> <param name="count_in" type="data" format="mothur.count_table" optional="true" label="count - a count_table" help="generated by count.seqs"/> <param name="name_in" type="data" format="mothur.names" optional="true" label="name - Sequences Name reference"/> <param name="group_in" type="data" format="mothur.groups" optional="true" label="group - Sequences Groups"/> <param name="alignreport_in" type="data" format="mothur.align.report" optional="true" label="alignreport - Align Report"/> <param name="list_in" type="data" format="mothur.list" optional="true" label="list - OTU List"/> <param name="taxonomy_in" type="data" format="mothur.seq.taxonomy" optional="true" label="taxonomy - Taxonomy"/> <param name="dups" type="boolean" truevalue="dups" falsevalue="false" checked="true" label="dups - Apply to duplicates"/> <expand macro="param-savelog"/> </inputs> <outputs> <expand macro="logfile-output"/> <data name="fasta_out" format_source="fasta_in" from_work_dir="fasta_in*.pick.*" label="${tool.name} on ${on_string}: pick.fasta"> <filter>fasta_in</filter> </data> <data name="fastq_out" format_source="fastq_in" from_work_dir="fastq_in*.pick.*" label="${tool.name} on ${on_string}: pick.fastq"> <filter>fastq_in</filter> </data> <data name="count_out" format_source="count_in" from_work_dir="count_in*.pick.*" label="${tool.name} on ${on_string}: pick.count"> <filter>count_in</filter> </data> <data name="qfile_out" format_source="qfile_in" from_work_dir="qfile_in*.pick.*" label="${tool.name} on ${on_string}: pick.qfile"> <filter>qfile_in</filter> </data> <data name="name_out" format="mothur.names" from_work_dir="name_in*.pick.*" label="${tool.name} on ${on_string}: pick.names"> <filter>name_in</filter> </data> <data name="group_out" format="mothur.groups" from_work_dir="group_in*.pick.*" label="${tool.name} on ${on_string}: pick.groups"> <filter>group_in</filter> </data> <data name="alignreport_out" format="mothur.align.report" from_work_dir="alignreport_in*.pick.*" label="${tool.name} on ${on_string}: pick.align.report"> <filter>alignreport_in</filter> </data> <data name="list_out" format="mothur.list" from_work_dir="list_in*.pick.*" label="${tool.name} on ${on_string}: pick.list"> <filter>list_in</filter> </data> <data name="taxonomy_out" format="mothur.seq.taxonomy" from_work_dir="taxonomy_in*.pick.*" label="${tool.name} on ${on_string}: pick.taxonomy"> <filter>taxonomy_in</filter> </data> </outputs> <tests> <test> <param name="accnos" value="Mock_S280_L001_R1_001_small.trim.contigs.bad.accnos"/> <param name="fasta_in" value="Mock_S280_L001_R1_001_small.trim.contigs.fasta"/> <param name="dups" value=""/> <output name="fasta_out" md5="f9335b6b70dc639e420d33809e51431d"/> <param name="savelog" value="true"/> <expand macro="logfile-test"/> </test> <test> <param name="accnos" value="Mock_S280_L001_R1_001_small.trim.contigs.bad.accnos"/> <param name="fastq_in" value="Mock_S280_L001_R1_001_small.fastq"/> <output name="fastq_out" md5="81d026f969e15b8c8701f8dc5f3a6904"/> <param name="savelog" value="true"/> <expand macro="logfile-test"/> </test> <test> <!-- test two input files --> <param name="accnos" value="Mock_S280_L001_R1_001_small.trim.contigs.bad.accnos"/> <param name="fasta_in" value="Mock_S280_L001_R1_001_small.trim.contigs.fasta"/> <param name="fastq_in" value="Mock_S280_L001_R1_001_small.fastq"/> <param name="dups" value="false"/> <output name="fasta_out" md5="f9335b6b70dc639e420d33809e51431d"/> <output name="fastq_out" md5="81d026f969e15b8c8701f8dc5f3a6904"/> <param name="savelog" value="true"/> <expand macro="logfile-test"/> </test> <test> <param name="accnos" value="amazon.bad.accnos"/> <param name="count_in" value="amazon.count_table"/> <output name="count_out" md5="6892dd99850ce9e9f8f15e77b28f57e2"/> <param name="savelog" value="true"/> <expand macro="logfile-test"/> </test> </tests> <help><![CDATA[ @MOTHUR_OVERVIEW@ **Command Documentation** The get.seqs_ command takes a list of sequence names and either a fasta, name_, group_, list_, align.report_ or taxonomy_ file to generate a new file that contains only the sequences in the list. This command may be used in conjunction with the list.seqs_ command to help screen a sequence collection. .. _name: https://www.mothur.org/wiki/Name_file .. _group: https://www.mothur.org/wiki/Group_file .. _list: https://www.mothur.org/wiki/List_file .. _align.report: https://www.mothur.org/wiki/Align.seqs .. _taxonomy: https://www.mothur.org/wiki/Taxonomy_outline .. _list.seqs: https://www.mothur.org/wiki/list.seqs .. _get.seqs: https://www.mothur.org/wiki/Get.seqs v.1.27.0 : Updated to Mothur 1.33, added count and fastq params ]]></help> <expand macro="citations"/> </tool>