Mercurial > repos > bgruening > nanopolish_polya
diff nanopolish_polya.xml @ 0:7739a9b0dd83 draft
planemo upload for repository https://github.com/bgruening/galaxytools/tree/master/tools/nanopolish commit 89078a214cefd31d28da75ddebb21f546fba79df-dirty
author | bgruening |
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date | Wed, 19 Jun 2019 07:00:20 -0400 |
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children | 449e9aeded2d |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/nanopolish_polya.xml Wed Jun 19 07:00:20 2019 -0400 @@ -0,0 +1,126 @@ +<tool id="nanopolish_polya" name="Nanopolish polyA" version="0.1.0"> + <description>- Estimate the length of the poly-A tail on direct RNA reads.</description> + <macros> + <import>macros.xml</import> + </macros> + <expand macro="requirements" /> + <command detect_errors="exit_code"><![CDATA[ + ln -s '$input_merged' reads.fasta && + + #if $input_reads_raw.extension == 'fast5': + mkdir fast5_files && ln -s '$input_reads_raw' fast5_files/read1.fast5 && + + #else if $input_reads_raw.extension == 'fast5.tar': + ln -s '$input_reads_raw' fast5_files.tar && + mkdir fast5_files && tar -xf fast5_files.tar -C fast5_files && + + #else if $input_reads_raw.extension == 'fast5.tar.bz2': + ln -s '$input_reads_raw' fast5_files.tar.bz2 && + mkdir fast5_files && tar -xjf fast5_files.tar.bz2 -C fast5_files && + + #else: + ln -s '$input_reads_raw' fast5_files.tar.gz && + mkdir fast5_files && tar -xzf fast5_files.tar.gz -C fast5_files && + + #end if + + nanopolish index + -d fast5_files/ + #if $adv.input_seq_summary: + -s '$adv.input_seq_summary' + #end if + reads.fasta && + + ln -s '$b' reads.bam && + ln -s '${b.metadata.bam_index}' reads.bam.bai && + #if $reference_source.reference_source_selector == 'history': + ln -f -s '$reference_source.ref_file' genome.fa && + #else: + ln -f -s '$reference_source.ref_file.fields.path' genome.fa && + #end if + + nanopolish polya + -r reads.fasta + -b reads.bam + -g genome.fa + --threads "\${GALAXY_SLOTS:-4}" + #if $w and str($w).strip(): + -w "${w}" + #end if + > polya_results.tsv + ]]></command> + <inputs> + <!-- index inputs --> + <param type="data" name="input_merged" format="fasta,fastq" label="Basecalled merged reads.fa"/> + <param type="data" name="input_reads_raw" format="h5,fast5.tar.gz,fast5.tar.bz2,fast5.tar" label="Flat archive file of raw fast5 files"/> + + <param type="data" argument="-b" format="bam" label="Reads aligned to the reference genome" /> + <conditional name="reference_source"> + <param name="reference_source_selector" type="select" label="Load reference genome from"> + <option value="cached">Local cache</option> + <option value="history">History</option> + </param> + <when value="cached"> + <param name="ref_file" type="select" label="Using reference genome" help="REFERENCE_SEQUENCE"> + <options from_data_table="all_fasta"> + </options> + <validator type="no_options" message="A built-in reference genome is not available for the build associated with the selected input file"/> + </param> + </when> + <when value="history"> + <param name="ref_file" type="data" format="fasta" label="Use the following dataset as the reference sequence" help="REFERENCE_SEQUENCE; You can upload a FASTA sequence to the history and use it as reference" /> + </when> + </conditional> + + <section name="adv" title="Optional data inputs"> + <!-- optional inputs --> + <param type="data" name="input_seq_summary" format="txt" optional="true" label="Sequencing summary file from albacore" help="(-s)"/> + </section> + + <param argument="-w" type="text" optional="true" + label="only compute the poly-A lengths for reads in window STR (format: ctg:start_id-end_id)" /> + + </inputs> + + <outputs> + <data name="polya_results" format="tabular" from_work_dir="polya_results.tsv" label="called methylation sites" /> + </outputs> + <tests> + <test> + <param name="input_merged" ftype="fastq" value="30xpolyA-small-subset.fastq" /> + <param name="input_reads_raw" ftype="fast5.tar.gz" value="fast5_files_30xpolyA-small-subset.tar.gz" /> + <param name="b" value="30xpolyA-small-subset.sorted.bam" /> + <param name="reference_source_selector" value="history" /> + <param name="ref_file" value="enolase_reference.fas" /> + <!-- <param name="w" value="tig00000001:200000-202000" /> --> + <output name="polya_results" file="30xpolyA-small-subset-results.tsv" /> + </test> + <test> + <param name="input_merged" ftype="fastq" value="30xpolyA-small-subset.fastq" /> + <param name="input_reads_raw" ftype="fast5.tar.gz" value="fast5_files_30xpolyA-small-subset.tar.gz" /> + <param name="b" value="30xpolyA-small-subset.sorted.bam" /> + <param name="reference_source_selector" value="history" /> + <param name="ref_file" value="enolase_reference.fas" /> + <param name="w" value="YHR174W:600-900" /> + <output name="polya_results" file="30xpolyA-small-subset-win-results.tsv" /> + </test> + <test> + <param name="input_merged" ftype="fastq" value="30xpolyA-small-subset.fastq" /> + <param name="input_reads_raw" ftype="fast5.tar" value="fast5_files_30xpolyA-small-subset.tar" /> + <param name="b" value="30xpolyA-small-subset.sorted.bam" /> + <param name="reference_source_selector" value="history" /> + <param name="ref_file" value="enolase_reference.fas" /> + <param name="w" value="YHR174W:600-900" /> + <output name="polya_results" file="30xpolyA-small-subset-win-results-t3.tsv" /> + </test> + </tests> + <help><![CDATA[ + Usage: nanopolish polya [OPTIONS] --reads reads.fa --bam alignments.bam --genome genome.fa + Estimate the length of the poly-A tail on direct RNA reads + + Quickstart tutorial and manual available at: + http://nanopolish.readthedocs.io/en/latest/quickstart_polya.html + + ]]></help> + <expand macro="citations" /> +</tool>