Mercurial > repos > iuc > trycycler_consensus
view trycycler_consensus.xml @ 4:43af166bc01e draft
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/trycycler commit e093c3f4fa599c1cb5cfc6f98e11ff1070ce440f"
author | iuc |
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date | Mon, 13 Dec 2021 21:17:36 +0000 |
parents | e59bee4565b3 |
children | 9ded6109434a |
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<tool id='trycycler_consensus' name='Trycycler consensus' version='@TOOL_VERSION@' profile='20.01'> <description>generate a consensus contig sequence for each cluster</description> <macros> <import>macros.xml</import> </macros> <expand macro='edam_ontology' /> <expand macro='requirements' /> <version_command>trycycler --version</version_command> <command detect_errors='exit_code'><![CDATA[ mkdir -p 'selected_cluster' && ln -s '${cluster_all_seqs}' 'selected_cluster/2_all_seqs.fasta' && ln -s '${reconcile_msa}' 'selected_cluster/3_msa.fasta' && ln -s '${partition_reads}' 'selected_cluster/4_reads.fastq' && trycycler consensus --cluster_dir 'selected_cluster' #if $linear --linear #end if --min_aligned_len $min_aligned_len --min_read_cov $min_read_cov --threads \${GALAXY_SLOTS:-2} && mv 'selected_cluster/7_final_consensus.fasta' $consensus ]]> </command> <inputs> <param name='cluster_all_seqs' type='data' format='fasta' label='Reconciled cluster' help='Reconciled sequences file' /> <param name='reconcile_msa' type='data' format='fasta' label='Reconcile msa' help='Multiple sequence alignment file' /> <param name='partition_reads' type='data' format='fastq' label='Partition reads' help='Partitioned reads' /> <param name='reads' type='data' format='fastq,fastq.gz' label='Long-read datasets' help='Long reads (FASTQ format) used to generate the assemblies' /> <param argument='--linear' type='boolean' truevalue='--linear' falsevalue='' label='Input contigs are not circular' help='Use this option if your input contigs are not circular. It will disable the circularisation-correction steps in Trycycler reconcile.' /> <param argument='--min_aligned_len' type='integer' min='500' max='3500' value='1000' label='Min bases aligned' help='Reads with less than this many bases aligned (default = 1000) will be ignored.' /> <param argument='--min_read_cov' type='integer' min='0' max='100' value='90' label='Min read length covered by alignments' help='Reads with less than this percentage of their length covered by alignments (default = 90.0) will be ignored.' /> </inputs> <outputs> <data name='consensus' format='fasta' label='${tool.name} on ${on_string}' /> </outputs> <tests> <test> <param name='cluster_all_seqs' value='reconciled_cluster_01.fasta' /> <param name='reconcile_msa' value='aligned_cluster_01.fasta' /> <param name='partition_reads' value='partition_01.fastq' /> <param name='reads' value='reads.fastq.gz' /> <param name='min_aligned_len' value='1200' /> <param name='min_read_cov' value='95' /> <output name='consensus' file='consensus_sequence_01.fasta' /> </test> <test> <param name='cluster_all_seqs' value='reconciled_cluster_02.fasta' /> <param name='reconcile_msa' value='aligned_cluster_02.fasta' /> <param name='partition_reads' value='partition_01.fastq' /> <param name='reads' value='reads.fastq.gz' /> <param name='min_aligned_len' value='1100' /> <param name='min_read_cov' value='90' /> <output name='consensus' file='consensus_sequence_02.fasta' /> </test> <test> <param name='cluster_all_seqs' value='reconciled_cluster_03.fasta' /> <param name='reconcile_msa' value='aligned_cluster_03.fasta' /> <param name='partition_reads' value='partition_01.fastq' /> <param name='reads' value='reads.fastq.gz' /> <param name='min_aligned_len' value='1300' /> <param name='min_read_cov' value='97' /> <output name='consensus' file='consensus_sequence_03.fasta' /> </test> <test> <param name='cluster_all_seqs' value='reconciled_cluster_03.fasta' /> <param name='reconcile_msa' value='aligned_cluster_03.fasta' /> <param name='partition_reads' value='partition_01.fastq' /> <param name='reads' value='reads.fastq.gz' /> <param name='min_aligned_len' value='1000' /> <param name='min_read_cov' value='87' /> <output name='consensus' file='consensus_sequence_04.fasta' /> </test> </tests> <help><![CDATA[ .. class:: infomark **Purpose** **Trycycler consensus** generate a consensus contig sequence for each cluster. It does this by converting the MSA into a graph form. When there is a tie between options, Trycycler aligns the reads to the alternative sequences and chooses the option with the best read alignment scores. :: GGAGGAGCTTTT-CGCCGCAGTCAACGAA-TAGCGTCTGAAAACGTGTATCAT GGAGGAGCTTTTTCGCCGCAGTCAAC--A-TAGCGTCTGAAAACGTGTATCAT GGAGGAGCTTTTTCGCCGCAGTCAAC--ATTAGCGTCTGAAAACGTGTATCAT GGAGGAGCTTTTTCGCCGCAGTCAAC--A-TAGCGTCTGAAAACGTGTATCAT GGAGGAGCTTTT-CGCCGCAGTCAAC--A-TAGCGTCTGAAAACGTGTATCAT From the hypothetical MSA, Trycycler generates a variation graph: :: ↗ - ↘ ↗ GAA- ↘ ↗ T ↘ ↗ --A- ↘ GGAGGAGCTTTT → T → CGCCGCAGTCAAC → --AT → TAGCGTCTGAAAACGTGTATCAT ↘ T ↗ ↘ --A- ↗ ↘ - ↗ ↘ --A- ↗ The first thing Trycycler uses to choose variants is minimum total Hamming distance to the other variants. In cases of a minimum total Hamming distance tie, Trycycler will align the reads to each possibility and choose the option with the highest total read alignment score. Read alignment scores are calculated using a simple scheme: match score = 1, mismatch penalty = 1, gap open/extension penalty = 1. More information in the `documentation <https://github.com/rrwick/Trycycler/wiki/How-variants-are-chosen-for-the-consensus-sequence/>`_. ---- .. class:: infomark **Input** This tool requires the output generated by **Trycylcler reconcile**, **Trycycler msa** and **Trycycler partition**. ---- .. class:: infomark **Output** It generates a fasta file with the consesus sequence the cluster. ---- .. class:: infomark @PIPELINE@ ]]> </help> <expand macro='citations' /> </tool>