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planemo upload for repository https://github.com/ErasmusMC-Bioinformatics/galaxytools-emc/tree/master/tools/mycrobiota commit aadbfac9c48191cac625f10590082a6d1a0bfd09
author | erasmus-medical-center |
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date | Tue, 29 Jan 2019 12:13:23 -0500 |
parents | 607c5e7e0a64 |
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<tool id="mycrobiota_subsample_add_discarded_samples" name="Recover samples" version="0.1" profile="16.07"> <description> discarded by sub.sample</description> <requirements> <requirement type="package" version="1.36.1">mothur</requirement> </requirements> <command detect_errors="aggressive"><![CDATA[ ln -s "$in_fasta" fasta.dat && ln -s "$in_group" group.dat && ln -s "$in_fasta_subsampled" fasta2.dat && ln -s "$in_group_subsampled" group2.dat ## mothur count.groups on in_fasta && echo 'count.groups(group=group.dat)' | sed 's/ //g' | mothur ## get group names with fewer than threshold reads and make a dash-separated list && samples=`python -c "print('-'.join([g[0] for g in [ l.strip().split('\t') for l in open('group.count.summary').readlines() ] if int(g[1]) < $threshold]))"` ## get.groups on in_fasta with this list of groups, if list not empty, otherwise create empty file && if [ -z "\$samples"]; then cp fasta2.dat final_fasta; cp group2.dat final_group; else echo "get.groups(fasta=fasta.dat, group=group.dat, groups=\$samples)" | sed 's/ //g' | mothur; ## merge selected reads (fasta.pick.dat) with the fasta file from after sub.sample echo "merge.files(input=fasta2.dat-fasta.pick.dat, output=final_fasta)" | sed 's/ //g' | mothur; ## merge group files echo "merge.files(input=group2.dat-group.pick.dat, output=final_group)" | sed 's/ //g' | mothur; fi ]]></command> <inputs> <param name="in_fasta" type="data" format="fasta" label="Fasta before subsample"/> <param name="in_fasta_subsampled" type="data" format="fasta" label="Fasta after subsample"/> <param name="in_group" type="data" format="mothur.groups" label="Group file before subsample"/> <param name="in_group_subsampled" type="data" format="mothur.groups" label="Group file after subsample"/> <param name="threshold" type="integer" value="" min="0" label="Subsample level - cutoff value used in the subsampling" help="any samples with fewer reads than this value would have been discarded by sub.sample, but we want to add them back in" /> </inputs> <outputs> <data name="out_fasta" format="fasta" from_work_dir="final_fasta" label="${tool.name} on ${on_string}: fasta"/> <data name="out_group" format="mothur.groups" from_work_dir="final_group" label="${tool.name} on ${on_string}: group"/> </outputs> <tests> <test> <param name="in_fasta" value="fasta_before_subsample_small.fasta" ftype="fasta"/> <param name="in_fasta_subsampled" value="fasta_after_subsample_small.fasta" ftype="fasta"/> <param name="in_group" value="groups_before_subsample_small.groups" ftype="mothur.groups"/> <param name="in_group_subsampled" value="groups_after_subsample_small.groups" ftype="mothur.groups"/> <param name="threshold" value="3"/> <output name="out_fasta" file="recovered.fasta"/> <output name="out_group" file="recovered.groups"/> </test> <test><!-- test case where nothing was discarded --> <param name="in_fasta" value="fasta_before_subsample_small.fasta" ftype="fasta"/> <param name="in_fasta_subsampled" value="fasta_after_subsample_small.fasta" ftype="fasta"/> <param name="in_group" value="groups_before_subsample_small.groups" ftype="mothur.groups"/> <param name="in_group_subsampled" value="groups_after_subsample_small.groups" ftype="mothur.groups"/> <param name="threshold" value="1"/> <output name="out_fasta" file="fasta_after_subsample_small.fasta"/> <output name="out_group" file="groups_after_subsample_small.groups"/> </test> </tests> <help><![CDATA[ **What it does** filter fasta file by group based on number of sequences in the group. ]]></help> <citations> </citations> </tool>