Mercurial > repos > iuc > funannotate_annotate
diff funannotate_annotate.xml @ 10:d0336d67702b draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/main/tools/funannotate commit 737d7e9a31c9d340a38ddfef3ac20847989718e0
author | iuc |
---|---|
date | Sun, 11 Feb 2024 00:08:00 +0000 |
parents | 3bbe70fef6df |
children | 9c15ca7e764e |
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--- a/funannotate_annotate.xml Mon Dec 11 19:18:59 2023 +0000 +++ b/funannotate_annotate.xml Sun Feb 11 00:08:00 2024 +0000 @@ -1,4 +1,4 @@ -<tool id="funannotate_annotate" name="Funannotate functional" profile="20.01" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@"> +<tool id="funannotate_annotate" name="Funannotate functional" profile="20.01" version="@TOOL_VERSION@+galaxy5"> <description>annotation</description> <macros> <import>macros.xml</import> @@ -72,27 +72,14 @@ && -## funannotate sometimes leaves multiple *part.tbl and *part.sqn files +## Funannotate sometimes leaves multiple *part.tbl and *part.sqn files: ## https://github.com/nextgenusfs/funannotate/issues/777 +## The partial tbl files are combined by funannotate and are deleted below. +## The sqn files are discrete and are collected with discover_datasets. find output/annotate_results --regex ".*part_[0-9]+\.\(sqn\|tbl\)$" +-regex ".*part_[0-9]+\.\(tbl\)$" -delete -&& - -mv output/annotate_results/*.gbk out.gbk && -mv output/annotate_results/*.annotations.txt out.annotations.txt && -mv output/annotate_results/*.contigs.fsa out.contigs.fsa && -mv output/annotate_results/*.agp out.agp && -mv output/annotate_results/*.tbl out.tbl && -mv output/annotate_results/*.sqn out.sqn && -mv output/annotate_results/*.scaffolds.fa out.scaffolds.fa && -mv output/annotate_results/*.proteins.fa out.proteins.fa && -mv output/annotate_results/*.mrna-transcripts.fa out.mrna-transcripts.fa && -mv output/annotate_results/*.cds-transcripts.fa out.cds-transcripts.fa && -mv output/annotate_results/*.gff3 out.gff3 && -mv output/annotate_results/*.discrepency.report.txt out.discrepency.report.txt && -mv output/annotate_results/*.stats.json out.stats.json ]]></command> <inputs> @@ -164,43 +151,44 @@ </param> </inputs> <outputs> - <data name='gbk' format='genbank' label="${tool.name} on ${on_string}: annotated genome (genbank)" from_work_dir="out.gbk"> + <data name='gbk' format='genbank' label="${tool.name} on ${on_string}: annotated genome (genbank)" from_work_dir="output/annotate_results/*.gbk"> <filter>outputs and 'gbk' in outputs</filter> </data> - <data name='annot' format='tabular' label="${tool.name} on ${on_string}: all annotations" from_work_dir="out.annotations.txt"> + <data name='annot' format='tabular' label="${tool.name} on ${on_string}: all annotations" from_work_dir="output/annotate_results/*.annotations.txt"> <filter>outputs and 'annotations' in outputs</filter> </data> - <data name='contigs_fsa' format='fasta' label="${tool.name} on ${on_string}: contigs fasta, split at gaps" from_work_dir="out.contigs.fsa"> + <data name='contigs_fsa' format='fasta' label="${tool.name} on ${on_string}: contigs fasta, split at gaps" from_work_dir="output/annotate_results/*.contigs.fsa"> <filter>outputs and 'contigs_fsa' in outputs</filter> </data> - <data name='agp' format='tabular' label="${tool.name} on ${on_string}: AGP file" from_work_dir="out.agp"> + <data name='agp' format='tabular' label="${tool.name} on ${on_string}: AGP file" from_work_dir="output/annotate_results/*.agp"> <filter>outputs and 'agp' in outputs</filter> </data> - <data name='tbl' format='txt' label="${tool.name} on ${on_string}: NCBI tbl annotation file" from_work_dir="out.tbl"> + <data name='tbl' format='txt' label="${tool.name} on ${on_string}: NCBI tbl annotation file" from_work_dir="output/annotate_results/*.tbl"> <filter>outputs and 'tbl' in outputs</filter> </data> - <data name='sqn' format='txt' label="${tool.name} on ${on_string}: NCBI Sequin genome" from_work_dir="out.sqn"> + <collection name="sqn" type="list" label="${tool.name} on ${on_string}: NCBI Sequin genome files"> + <discover_datasets pattern="(?P<designation>.+)\.sqn" directory="output/annotate_results" format="txt" recurse="false"/> <filter>outputs and 'sqn' in outputs</filter> - </data> - <data name='fa_scaffolds' format='fasta' label="${tool.name} on ${on_string}: scaffolds sequences" from_work_dir="out.scaffolds.fa"> + </collection> + <data name='fa_scaffolds' format='fasta' label="${tool.name} on ${on_string}: scaffolds sequences" from_work_dir="output/annotate_results/*.scaffolds.fa"> <filter>outputs and 'scaffolds_fa' in outputs</filter> </data> - <data name='fa_proteins' format='fasta' label="${tool.name} on ${on_string}: protein sequences" from_work_dir="out.proteins.fa"> + <data name='fa_proteins' format='fasta' label="${tool.name} on ${on_string}: protein sequences" from_work_dir="output/annotate_results/*.proteins.fa"> <filter>outputs and 'proteins_fa' in outputs</filter> </data> - <data name='fa_transcripts_mrna' format='fasta' label="${tool.name} on ${on_string}: transcript mRNA sequences" from_work_dir="out.mrna-transcripts.fa"> + <data name='fa_transcripts_mrna' format='fasta' label="${tool.name} on ${on_string}: transcript mRNA sequences" from_work_dir="output/annotate_results/*.mrna-transcripts.fa"> <filter>outputs and 'mrna_transcripts_fa' in outputs</filter> </data> - <data name='fa_transcripts_cds' format='fasta' label="${tool.name} on ${on_string}: transcript CDS sequences" from_work_dir="out.cds-transcripts.fa"> + <data name='fa_transcripts_cds' format='fasta' label="${tool.name} on ${on_string}: transcript CDS sequences" from_work_dir="output/annotate_results/*.cds-transcripts.fa"> <filter>outputs and 'cds_transcripts_fa' in outputs</filter> </data> - <data name='gff3' format='gff3' label="${tool.name} on ${on_string}: annotation (GFF3)" from_work_dir="out.gff3"> + <data name='gff3' format='gff3' label="${tool.name} on ${on_string}: annotation (GFF3)" from_work_dir="output/annotate_results/*.gff3"> <filter>outputs and 'gff3' in outputs</filter> </data> - <data name='tbl2asn_report' format='txt' label="${tool.name} on ${on_string}: tbl2asn summary report of annotated genome" from_work_dir="out.discrepency.report.txt"> + <data name='tbl2asn_report' format='txt' label="${tool.name} on ${on_string}: tbl2asn summary report of annotated genome" from_work_dir="output/annotate_results/*.discrepency.report.txt"> <filter>outputs and 'discrepency' in outputs</filter> </data> - <data name='stats' format='json' label="${tool.name} on ${on_string}: stats" from_work_dir="out.stats.json"> + <data name='stats' format='json' label="${tool.name} on ${on_string}: stats" from_work_dir="output/annotate_results/*.stats.json"> <filter>outputs and 'gbk' in outputs</filter> </data> <data name='must_fix' format='json' label="${tool.name} on ${on_string}: Gene Name/Product must-fix" from_work_dir="output/annotate_results/Gene2Products.must-fix.txt"> @@ -248,11 +236,13 @@ <has_text text="locus_tag" /> </assert_contents> </output> - <output name="sqn"> - <assert_contents> - <has_text text="Seq-submit" /> - </assert_contents> - </output> + <output_collection name="sqn" type="list"> + <element name="Genus_species"> + <assert_contents> + <has_text text="Seq-submit" /> + </assert_contents> + </element> + </output_collection> <output name="fa_scaffolds"> <assert_contents> <has_text text=">sample" /> @@ -340,11 +330,13 @@ <has_text text="locus_tag" /> </assert_contents> </output> - <output name="sqn"> - <assert_contents> - <has_text text="Seq-submit" /> - </assert_contents> - </output> + <output_collection name="sqn" type="list"> + <element name="Genus_species"> + <assert_contents> + <has_text text="Seq-submit" /> + </assert_contents> + </element> + </output_collection> <output name="fa_scaffolds"> <assert_contents> <has_text text=">sample" />