Mercurial > repos > iuc > featurecounts
comparison featurecounts.xml @ 35:519ae9e6fdb9 draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/featurecounts commit eb563889f227d5c473e2bad2cf9a513e41d03fca
| author | iuc |
|---|---|
| date | Thu, 24 Oct 2024 05:46:12 +0000 |
| parents | 12b3317716d3 |
| children | 39863c075dca |
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| 34:12b3317716d3 | 35:519ae9e6fdb9 |
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| 1 <tool id="featurecounts" name="featureCounts" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@" profile="20.09"> | 1 <tool id="featurecounts" name="featureCounts" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@" profile="20.09"> |
| 2 <description>Measure gene expression in RNA-Seq experiments from SAM or BAM files</description> | 2 <description>Measure gene expression in RNA-Seq experiments from SAM or BAM files</description> |
| 3 <macros> | 3 <macros> |
| 4 <token name="@TOOL_VERSION@">2.0.3</token> | 4 <token name="@TOOL_VERSION@">2.0.6</token> |
| 5 <token name="@VERSION_SUFFIX@">2</token> | 5 <token name="@VERSION_SUFFIX@">0</token> |
| 6 | 6 |
| 7 <macro name="conditional_gff_opions"> | 7 <macro name="conditional_gff_opions"> |
| 8 <param name="gff_feature_type" type="text" value="exon" argument="-t" label="GFF feature type filter" help="Specify the feature type. Only rows which have the matched matched feature type in the provided GTF annotation file will be included for read counting. `exon' by default."/> | 8 <param name="gff_feature_type" type="text" value="exon" argument="-t" label="GFF feature type filter" help="Specify the feature type. Only rows which have the matched matched feature type in the provided GTF annotation file will be included for read counting. `exon' by default."/> |
| 9 <param name="gff_feature_attribute" type="text" value="gene_id" argument="-g" label="GFF gene identifier" help="Specify the attribute type used to group features (eg. exons) into meta-features (eg. genes), when GTF annotation is provided. `gene_id' by default. This attribute type is usually the gene identifier. This argument is useful for the meta-feature level summarization. Ex: if the 9th column is 'gene_id "ENSG00000223972"; gene_name "DDX11L1" gene_source "havana"' (GTF) or 'gene_id=ENSG00000223972; gene_name=DDX11L1; gene_source=havana' (GFF), the available attributes for this feature are 'gene_id', 'gene_name' and 'gene_source'."/> | 9 <param name="gff_feature_attribute" type="text" value="gene_id" argument="-g" label="GFF gene identifier" help="Specify the attribute type used to group features (eg. exons) into meta-features (eg. genes), when GTF annotation is provided. `gene_id' by default. This attribute type is usually the gene identifier. This argument is useful for the meta-feature level summarization. Ex: if the 9th column is 'gene_id "ENSG00000223972"; gene_name "DDX11L1" gene_source "havana"' (GTF) or 'gene_id=ENSG00000223972; gene_name=DDX11L1; gene_source=havana' (GFF), the available attributes for this feature are 'gene_id', 'gene_name' and 'gene_source'."/> |
| 10 <param name="summarization_level" type="boolean" truevalue=" -f" falsevalue="" argument="-f" label="On feature level" help="If specified, read summarization will be performed at the feature level. By default (-f is not specified), the read summarization is performed at the meta-feature level."/> | 10 <param name="summarization_level" type="boolean" truevalue=" -f" falsevalue="" argument="-f" label="On feature level" help="If specified, read summarization will be performed at the feature level. By default (-f is not specified), the read summarization is performed at the meta-feature level."/> |
| 13 <xrefs> | 13 <xrefs> |
| 14 <xref type="bio.tools">featurecounts</xref> | 14 <xref type="bio.tools">featurecounts</xref> |
| 15 </xrefs> | 15 </xrefs> |
| 16 <requirements> | 16 <requirements> |
| 17 <requirement type="package" version="@TOOL_VERSION@">subread</requirement> | 17 <requirement type="package" version="@TOOL_VERSION@">subread</requirement> |
| 18 <requirement type="package" version="1.16.1">samtools</requirement> | 18 <requirement type="package" version="1.21">samtools</requirement> |
| 19 </requirements> | 19 </requirements> |
| 20 | 20 |
| 21 <version_command>featureCounts -v 2>&1 | grep .</version_command> | 21 <version_command>featureCounts -v 2>&1 | grep .</version_command> |
| 22 <command detect_errors="exit_code"><![CDATA[ | 22 <command detect_errors="exit_code"><![CDATA[ |
| 23 ## Export fc path for its built-in annotation | 23 ## Export fc path for its built-in annotation |
| 625 497097 chr1 3204563 3207049 - | 625 497097 chr1 3204563 3207049 - |
| 626 497098 chr1 3411783 3411982 - | 626 497098 chr1 3411783 3411982 - |
| 627 497099 chr1 3660633 3661579 - | 627 497099 chr1 3660633 3661579 - |
| 628 ====== ==== ======= ======= ====== | 628 ====== ==== ======= ======= ====== |
| 629 | 629 |
| 630 These annotation files can be found in the `Subread package`_. You can see the version of Subread used by this wrapper in the tool form above under `Options > Requirements`. To create the files, the annotations were downloaded from NCBI RefSeq database and then adapted by merging overlapping exons from the same gene to form a set of disjoint exons for each gene. Genes with the same Entrez gene identifiers were also merged into one gene. See the `Subread User's Guide`_ for more information. Gene names can be obtained for these Entrez identifiers with the Galaxy **annotateMyIDs** tool. | 630 These annotation files can be found in the _`Subread package`_. You can see the version of Subread used by this wrapper in the tool form above under `Options > Requirements`. To create the files, the annotations were downloaded from NCBI RefSeq database and then adapted by merging overlapping exons from the same gene to form a set of disjoint exons for each gene. Genes with the same Entrez gene identifiers were also merged into one gene. See the `Subread User's Guide`_ for more information. Gene names can be obtained for these Entrez identifiers with the Galaxy **annotateMyIDs** tool. |
| 631 | 631 |
| 632 Output format | 632 Output format |
| 633 ------------- | 633 ------------- |
| 634 FeatureCounts produces a table containing counted reads, per gene, per row. Optionally the last column can be set to be the effective gene-length. These tables are compatible with the DESeq2, edgeR and limma-voom Galaxy wrappers by IUC. | 634 FeatureCounts produces a table containing counted reads, per gene, per row. Optionally the last column can be set to be the effective gene-length. These tables are compatible with the DESeq2, edgeR and limma-voom Galaxy wrappers by IUC. |
| 635 | 635 |
| 636 .. _Subread: http://subread.sourceforge.net/ | 636 .. _Subread: http://subread.sourceforge.net/ |
| 637 .. _`Subread User's Guide`: https://bioconductor.org/packages/release/bioc/vignettes/Rsubread/inst/doc/SubreadUsersGuide.pdf | 637 .. _`Subread User's Guide`: https://bioconductor.org/packages/release/bioc/vignettes/Rsubread/inst/doc/SubreadUsersGuide.pdf |
| 638 .. _`Subread package`: https://sourceforge.net/projects/subread/files/ | |
| 639 ]]></help> | 638 ]]></help> |
| 640 <citations> | 639 <citations> |
| 641 <citation type="doi">10.1093/bioinformatics/btt656</citation> | 640 <citation type="doi">10.1093/bioinformatics/btt656</citation> |
| 642 </citations> | 641 </citations> |
| 643 </tool> | 642 </tool> |
