Mercurial > repos > gaelcge > r_signac_galaxy
diff signac_geneactivity.xml @ 0:6e0b320d8b6a draft default tip
"planemo upload commit dc808171975d0012e25bd7b32adc7a5a5c56a145-dirty"
author | gaelcge |
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date | Tue, 02 Aug 2022 19:11:27 +0000 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/signac_geneactivity.xml Tue Aug 02 19:11:27 2022 +0000 @@ -0,0 +1,32 @@ +<tool id="signac_geneactivity" name="Gene Activity" version="0.1.0" python_template_version="3.5"> +<description>Create gene activity matrix</description> +<macros> + <import>signac_macros.xml</import> +</macros> +<expand macro="requirements"/> +<stdio> + <exit_code range="1:" /> +</stdio> +<command><![CDATA[ + ln -s $fragment_file fragments.tsv.gz && + ln -s $fragment_index_file fragments.tsv.gz.tbi && + Rscript '${__tool_directory__}'/signac-geneactivity.R --signac-object $signac_object --fragment-file fragments.tsv.gz --assay $assay --features $features --extend-upstream $extend_upstream --extend-downstream $extend_downstream --biotypes $biotypes --max-width $max_width --output-object-file $rds_sparse_matrix +]]></command> +<inputs> + <param type="data" name="signac_object" label="Signac object." format="rdata" multiple="false" optional="false"/> + <param type="data" name="fragment_file" label="Select the fragment file." format="bgzip" multiple="false" optional="false"/> + <param type="data" name="fragment_index_file" label="Select the fragment index file." format="text" multiple="false" optional="false"/> + <param type="text" name="assay" format="txt" value="NULL" label="Name of assay to use. If blank, use the default assay." multiple="false" optional="true"/> + <param type="data" name="features" label="Features (If NULL, use all features)" format="txt" multiple="false" optional="true"/> + <param type="integer" name="extend_upstream" label="Number of bases to extend upstream of the TSS" multiple="false" optional="false" value="2000"/> + <param type="integer" name="extend_downstream" label="Number of bases to extend downstream of the TSS" multiple="false" optional="false" value="0"/> + <param type="text" name="biotypes" label="Gene biotypes to include. If NULL, use all biotypes in the gene annotation" multiple="false" optional="false" value="protein_coding"/> + <param type="integer" name="max_width" label="Maximum allowed gene width for a gene to be quantified" multiple="false" optional="false" value="500000"/> +</inputs> +<outputs> + <data name="rds_sparse_matrix" format="rdata" label="Sparse Matrix (Gene Activity)"/> +</outputs> +<help><![CDATA[ +Compute counts per cell in gene body and promoter region. + ]]></help> +</tool>