Mercurial > repos > iuc > coverm_genome
diff macros.xml @ 3:bb3f59096c8e draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tools/coverm commit 2d02165f40a9f8206a69716b2302bc58f5364982
| author | iuc |
|---|---|
| date | Wed, 26 Jul 2023 07:35:03 +0000 |
| parents | a671907f96fe |
| children | 0ff4b0e5a3bc |
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--- a/macros.xml Tue Mar 28 08:36:25 2023 +0000 +++ b/macros.xml Wed Jul 26 07:35:03 2023 +0000 @@ -1,13 +1,17 @@ <macros> + <token name="@TOOL_VERSION@">0.6.1</token> + <token name="@VERSION_SUFFIX@">1</token> + <token name="@PROFILE@">22.01</token> <xml name="requirements"> <requirements> <requirement type="package" version="@TOOL_VERSION@">coverm</requirement> </requirements> </xml> - <token name="@INPUT_FORMATS@">fasta,fastq,fastq.gz,fasta.gz</token> - <token name="@TOOL_VERSION@">0.6.1</token> - <token name="@VERSION_SUFFIX@">0</token> - <token name="@PROFILE@">22.01</token> + <xml name="bio_tools"> + <xrefs> + <xref type="bio.tools">coverm</xref> + </xrefs> + </xml> <xml name="citation"> <citations> <citation type="bibtex"> @@ -22,275 +26,315 @@ </citation> </citations> </xml> - <xml name="genome_opt"> - <conditional name="genome"> - <param name="ref_or_genome" type="select" label="Select if you want to specify additional genome files."> - <option value="genomic">yes</option> - <option value="none" selected="true">No (Only when BAM files are provided)</option> - </param> - <when value="none"> - <param argument="--single-genome" type="boolean" truevalue="--single-genome" falsevalue="" checked="false" label="All contigs are from the same genome."/> - <param type="text" name="separator" optional="true" label="Character, that separates genome names from contig names in the reference file." > - <sanitizer> - <valid initial="string.punctuation"> - </valid> - </sanitizer> - </param> + <xml name="mapped"> + <param name="mapped" type="select" label="Have the reads already been mapped to contigs?"> + <option value="mapped">Yes (no read mapping algorithm will be undertaken)</option> + <option value="not-mapped" selected="true">No</option> + </param> + </xml> + <xml name="assembly_mode"> + <param name="mode" type="select" label="Assembly mode?" help="Useful to know if contigs have been generated all samples together (co-assembly) or on each sample individually (individual assembly)"> + <option value="individual">Individual assembly (1 contig file per sample)</option> + <option value="co" selected="true">Co-assembly (1 contig file for several samples)</option> + </param> + </xml> + <xml name="mapped_params"> + <conditional name="mode"> + <expand macro="assembly_mode"/> + <when value="individual"> + <param argument="--bam-files" type="data" format="bam" label="BAM file(s)" help="These must be reference sorted (e.g. with samtools sort) unless sharded is specified, in which case they must be read name sorted (e.g. with samtools sort -n)."/> + </when> + <when value="co"> + <param argument="--bam-files" type="data" format="bam" multiple="true" label="BAM file(s)" help="These must be reference sorted (e.g. with samtools sort) unless sharded is specified, in which case they must be read name sorted (e.g. with samtools sort -n)."/> </when> - <when value="genomic"> - <conditional name="genomic"> - <param type="select" label="Reference genome source" name="source"> - <option value="history" selected="true">History</option> - <option value="builtin">Built-in</option> - </param> - <when value="history"> - <param type="data" name="fasta_history" multiple="true" label="FASTA files of each genome" format="fasta" /> - </when> - <when value="builtin"> - <param type="select" name="fasta_builtin" multiple="true" label="Reference genome(s)"> - <options from_data_table="all_fasta" /> - </param> - </when> - </conditional> + </conditional> + <param argument="--sharded" type="boolean" truevalue="--sharded" falsevalue="" checked="false" label="BAM file(s) read-sorted alignments of a set of reads mapped to multiple reference contig sets?" help="If set, it will choose the best hit for each read pair" /> + </xml> + <token name="@BAMS@"><![CDATA[ + #if $mapped.mode.mode == 'individual' + #set $fn = 'bam/' + re.sub('[^\s\w\-\\.]', '_', str($mapped.mode.bam_files.element_identifier)) + #silent $bam_fp.append( $fn ) +ln -s '$mapped.mode.bam_files' '$fn' && + #else + #for $i, $bam in enumerate($mapped.mode.bam_files) + #set $fn = 'bam/' + re.sub('[^\s\w\-\\.]', '_', str($bam.element_identifier)) + '_' + str($i) + #silent $bam_fp.append( $fn ) +ln -s '$bam' '$fn' && + #end for + #end if +]]></token> + <xml name="genomic"> + <conditional name="genomic"> + <param type="select" name="source" label="Source of FASTA files with each genome" > + <option value="history" selected="true">History</option> + <option value="builtin">Built-in</option> + </param> + <when value="history"> + <param argument="--genome-fasta-files" type="data" format="fasta" multiple="true" label="FASTA files of each genome"/> + </when> + <when value="builtin"> + <param argument="--genome-fasta-files" type="select" multiple="true" label="Reference genome(s)"> + <options from_data_table="all_fasta" /> + </param> </when> </conditional> </xml> - <xml name="genome"> - <conditional name="genome"> - <param name="ref_or_genome" type="select" label="Reference sequence mode" help="Select if you want to specify genome file(s) or a FASTA reference file or both. NOTE: If genomic FASTA files are specified, then reference is not needed as a reference FASTA file can be derived by concatenating input genomes. However, while not necessary, reference can be specified if an alternate reference sequence set is desired."> - <option value="genomic" selected="true">Reference genome</option> - <option value="reference">Contigs (e.g. concatenated genomes or metagenome assembly)</option> + <xml name="cond_single_genome"> + <conditional name="cond_single_genome"> + <param argument="--single-genome" type="select" label="Are all contigs from the same genome?"> + <option value="--single-genome">True</option> + <option value="">False</option> </param> - <when value="genomic"> - <conditional name="genomic"> - <param type="select" label="Reference genome source" name="source"> - <option value="history" selected="true">History</option> - <option value="builtin">Built-in</option> + <when value="--single-genome"/> + <when value=""> + <conditional name="genome_contig_definition"> + <param argument="choice" type="select" label="How to get genome names and contig names?"> + <option value="default" selected="true">Using default behavior</option> + <option value="genome-definition">Providing a file containing newline-separated list of genome name and contig</option> + <option value="separator">Providing character that separates genome names from contig names in the reference file</option> </param> - <when value="history"> - <param type="data" name="fasta_history" multiple="true" label="FASTA files of each genome" format="fasta" /> + <when value="default"/> + <when value="genome-definition"> + <param argument="--genome-definition" type="data" format="tabular" label="File containing newline-separated list of genome_name and contig, separated by tab, to define the genome of each contig." /> </when> - <when value="builtin"> - <param type="select" name="fasta_builtin" multiple="true" label="Reference genome(s)"> - <options from_data_table="all_fasta" /> - </param> - </when> - </conditional> - </when> - <when value="reference"> - <param type="data" name="ref_source" multiple="true" label="Contigs file(s)" format="fasta" help="If multiple references FASTA files are provided and 'sharded' is specified, then reads will be mapped to references separately as sharded BAMs."/> - <conditional name="cond_single_genome"> - <param name="single_genome" type="select" label="All contigs are from a single genome"> - <option value="--single-genome">True</option> - <option value="false">False</option> - </param> - <when value="--single-genome"> - <param type="data" name="genome_definition" format="tsv" optional="true" label="File containing newline-separated list of genome_name and contig, separated by tab, to define the genome of each contig." /> - </when> - <when value="false"> - <param type="text" argument="--separator" optional="true" label="Character, that separates genome names from contig names in the reference file." > + <when value="separator"> + <param argument="--separator" type="text" label="Character that separates genome names from contig names in the reference file." > <sanitizer> <valid initial="string.punctuation"> </valid> </sanitizer> </param> </when> - </conditional> - <conditional name="add_genome"> - <param name="add_genome" type="select" label="Add additional Genome Files"> - <option value="true">Yes</option> - <option value="false" selected="true">No</option> - </param> - <when value="true"> - <conditional name="add_genomic"> - <param type="select" label="Reference genome source" name="source"> - <option value="history" selected="true">History</option> - <option value="builtin">Built-in</option> - </param> - <when value="history"> - <param type="data" name="fasta_history" multiple="true" label="Single FASTA file of contigs" format="fasta" /> - </when> - <when value="builtin"> - <param type="select" name="fasta_builtin" multiple="true" label="Reference genome"> - <options from_data_table="all_fasta" /> - </param> - </when> - </conditional> - </when> - <when value="false"> - </when> </conditional> </when> </conditional> </xml> - <xml name="reads_for_contig"> - <conditional name="reads"> - <param type="select" label="Read type" name="read_type"> - <option value="paired">Paired end</option> - <option value="paired_collection" selected="true">Paired collection</option> - <option value="single">Single ended</option> - <option value="interleaved">Interleaved</option> - <option value="bam">BAM file(s)</option> - </param> + <token name="@INPUT_FORMATS@">fasta,fastq,fastq.gz,fasta.gz</token> + <xml name="read_type"> + <param name="type" type="select" label="Read type" > + <option value="single">Single end</option> + <option value="paired">Paired end</option> + <option value="paired_collection" selected="true">Paired collection</option> + <option value="interleaved">Interleaved</option> + </param> + </xml> + <xml name="paired_reads"> + <param name="paired_reads" type="data_collection" collection_type="list:paired" format="@INPUT_FORMATS@" label="Collection of paired-end FASTA/Q files(s) for mapping" help="One or more pairs of forward and reverse possibly gzipped FASTA/Q files for mapping in order." /> + </xml> + <xml name="individual_assembly_reads"> + <conditional name="read_type"> + <expand macro="read_type"/> + <when value="single"> + <param argument="--single" type="data" format="@INPUT_FORMATS@" label="Single Read" /> + </when> <when value="paired"> - <param type="data" format="@INPUT_FORMATS@" name="read1" multiple="true" label="Read1" /> - <param type="data" format="@INPUT_FORMATS@" name="read2" multiple="true" label="Read2" /> - <param type="data" name="ref_fasta_history" multiple="true" label="FASTA file(s) of contigs" format="fasta" /> + <param argument="-1" name="read1" type="data" format="@INPUT_FORMATS@" label="Forward FASTA/Q file for mapping" /> + <param argument="-2" name="read2" type="data" format="@INPUT_FORMATS@" label="Reverse FASTA/Q file for mapping" /> </when> <when value="paired_collection"> - <param type="data_collection" collection_type="list:paired" format="@INPUT_FORMATS@" name="paired_reads" label="One or more pairs of forward and reverse possibly gzipped FASTA/Q files for mapping in order" /> - <param type="data" name="ref_fasta_history" multiple="true" label="FASTA file(s) of contigs" format="fasta" /> - </when> - <when value="single"> - <param type="data" format="@INPUT_FORMATS@" multiple="true" name="single" label="Single Read" /> - <param type="data" name="ref_fasta_history" multiple="true" label="FASTA file(s) of contigs" format="fasta" /> + <expand macro="paired_reads"/> </when> <when value="interleaved"> - <param type="data" format="@INPUT_FORMATS@" multiple="true" name="single" label="Interleaved" /> - <param type="data" name="ref_fasta_history" multiple="true" label="FASTA file(s) of contigs" format="fasta" /> - </when> - <when value="bam"> - <param type="data" format="bam" name="bam" multiple="true" label="BAM file(s)" help="BAM file(s). These must be reference sorted (e.g. with samtools sort) unless sharded is specified, in which case they must be read name sorted (e.g. with samtools sort -n). When specified, no read mapping algorithm is undertaken."/> - <param type="data" name="ref_fasta_history" optional="true" multiple="true" label="FASTA file(s) of contigs" format="fasta" /> + <param argument="--interleaved" type="data" format="@INPUT_FORMATS@" label="Interleaved FASTA/Q files for mapping" /> </when> </conditional> - </xml> - <xml name="reads"> - <conditional name="reads"> - <param type="select" label="Read type" name="read_type"> - <option value="single">Single ended</option> - <option value="paired">Paired end</option> - <option value="paired_collection" selected="true">Paired collection</option> - <option value="interleaved">Interleaved</option> - <option value="bam">BAM file(s)</option> - </param> + </xml> + <xml name="ref_or_genome"> + <param name="ref_or_genome" type="select" label="Genome definition"> + <option value="contigs" selected="true">From contigs (e.g. concatenated genomes or metagenome assembly)</option> + <option value="genomic">From FASTA files with each genome</option> + </param> + </xml> + <xml name="individual_assembly_reference"> + <param argument="--reference" type="data" format="fasta" label="Contigs"/> + </xml> + <token name="@INDIVIDUAL_ASSEMBLY_READS@"><![CDATA[ + #set $reads = $mapped.mode.read_type + #if $reads.type == 'single' + #set $fn = "single/" + re.sub('[^\s\w\-\\.]', '_', str($reads.single.element_identifier)) + #silent $single_fp.append( $fn ) +ln -s '$reads.single' '$single_fp' && + #else if $reads.type == 'paired' + #set $fn = "fw/" + re.sub('[^\s\w\-\\.]', '_', str($reads.read1.element_identifier)) + #silent $fw_fp.append( $fn ) +ln -s '$reads.read1' '$fn' && + #set $fn = "rv/" + re.sub('[^\s\w\-\\.]', '_', str($reads.read2.element_identifier)) +ln -s '$reads.read2' '$fn' && + #silent $rv_fp.append( $fn ) + #else if $reads.type == 'paired_collection' + #set $id = re.sub('[^\s\w\-\\.]', '_', str($reads.paired_reads.element_identifier)) + #set $fn = "fw/" + $id + #silent $fw_fp.append( $fn ) +ln -s '$reads.paired_reads.forward' '$fn' && + #set $fn = "rv/" + $id + #silent $rv_fp.append( $fn ) +ln -s '$mreads.paired_reads.reverse' '${fn}' && + #else if $reads.type == 'interleaved' + #set $fn = "interl/" + re.sub('[^\s\w\-\\.]', '_', str($reads.interleaved.element_identifier)) + #silent $interl_fp.append( $fn ) +ln -s '$reads.interleaved' '$fn' && + #end if +]]></token> + <token name="@INDIVIDUAL_ASSEMBLY_REF@"><![CDATA[ + #set $fn = "ref/" + re.sub('[^\s\w\-\\.]', '_', str($ref.element_identifier)) + #silent $ref_fp.append( $fn ) +ln -s '$ref' '${fn}' && +]]></token> + <token name="@GENOME_FOR_READS@"><![CDATA[ + #if $mapped.mode.genome.genomic.source == 'history' + #for $i, $genome in enumerate($mapped.mode.genome.genomic.genome_fasta_files) + #set $fn = re.sub('[^\s\w\-\\.]', '_', str($genome.element_identifier)) + #silent $genome_fp.append( $fn ) +ln -s '$genome' '$fn' && + #end for + #else + #for $i, $genome in enumerate($mapped.mode.genome.genomic.genome_fasta_files) + #set $fn = re.sub('[^\s\w\-\\.]', '_', str($genome.fields.path.element_identifier)) + #silent $genome_fp.append( $fn ) +ln -s '$genome' '$fn' && + #end for + #end if +]]></token> + <xml name="co_assembly_reads"> + <conditional name="read_type"> + <expand macro="read_type"/> + <when value="single"> + <param argument="--single" type="data" format="@INPUT_FORMATS@" multiple="true" label="Single Read" /> + </when> <when value="paired"> - <param type="data" format="@INPUT_FORMATS@" name="read1" multiple="true" label="Read1" /> - <param type="data" format="@INPUT_FORMATS@" name="read2" multiple="true" label="Read2" /> - <expand macro="genome"/> + <param argument="-1" name="read1" type="data" format="@INPUT_FORMATS@" multiple="true" label="Forward FASTA/Q file(s) for mapping" /> + <param argument="-2" name="read2" type="data" format="@INPUT_FORMATS@" multiple="true" label="Reverse FASTA/Q file(s) for mapping" /> </when> <when value="paired_collection"> - <param type="data_collection" collection_type="list:paired" format="@INPUT_FORMATS@" name="paired_reads" label="Collection of paired-reads" help="One or more pairs of forward and reverse possibly gzipped FASTA/Q files for mapping in order." /> - <expand macro="genome"/> - </when> - <when value="single"> - <param type="data" format="@INPUT_FORMATS@" multiple="true" name="single" label="Single Read" /> - <expand macro="genome"/> + <expand macro="paired_reads"/> </when> <when value="interleaved"> - <param type="data" format="@INPUT_FORMATS@" multiple="true" name="single" label="Interleaved" /> - <expand macro="genome"/> - </when> - <when value="bam"> - <param type="data" format="bam" name="bam" multiple="true" label="BAM file(s)" help="BAM file(s). These must be reference sorted (e.g. with samtools sort) unless sharded is specified, in which case they must be read name sorted (e.g. with samtools sort -n). When specified, no read mapping algorithm is undertaken."/> - <expand macro="genome_opt"/> + <param argument="--interleaved" type="data" format="@INPUT_FORMATS@" multiple="true" label="Interleaved FASTA/Q files(s) for mapping" /> </when> </conditional> </xml> - <xml name="add_reads"> - <section name="add_reads" title="Add an additional read"> - <conditional name="extra_read"> - <param type="select" label="Read type" name="read_type"> - <option value="none" selected="true">None</option> - <option value="paired">Paired end</option> - <option value="paired_collection">Paired collection</option> - <option value="single">Single ended</option> - <option value="interleaved">Interleaved</option> - <option value="bam">BAM file(s)</option> - </param> - <when value="none"> - </when> - <when value="paired"> - <param type="data" format="@INPUT_FORMATS@" name="read1" multiple="true" label="Read1" /> - <param type="data" format="@INPUT_FORMATS@" name="read2" multiple="true" label="Read2" /> - </when> - <when value="paired_collection"> - <param type="data_collection" collection_type="list:paired" format="@INPUT_FORMATS@" name="paired_reads" label="One or more pairs of forward and reverse possibly gzipped FASTA/Q files for mapping in order" /> - </when> - <when value="single"> - <param type="data" format="@INPUT_FORMATS@" name="single" multiple="true" label="Single read" /> - </when> - <when value="interleaved"> - <param type="data" format="@INPUT_FORMATS@" multiple="true" name="single" label="Interleaved" /> - </when> - <when value="bam"> - <param type="data" format="bam" name="bam" multiple="true" label="BAM file(s)" /> - </when> - </conditional> - </section> + <xml name="co_assembly_reference"> + <param argument="--reference" type="data" format="fasta" multiple="true" label="Contigs" /> + <param argument="--sharded" type="boolean" truevalue="--sharded" falsevalue="" checked="false" label="Mapping reads to references separately as sharded BAMs?" /> + </xml> + <token name="@CO_ASSEMBLY_READS@"><![CDATA[ + #if $reads.type == 'single' + #for $i, $read in enumerate($reads.single) + #set $fn = "single/" + re.sub('[^\s\w\-\\.]', '_', str($read.element_identifier)) + "_single_" + str($i) + $extra + #silent $single_fp.append( $fn ) +ln -s '$read' '$fn' && + #end for + #else if $reads.type == 'paired' + #for $i, $read in enumerate($reads.read1) + #set $id = re.sub('[^\s\w\-\\.]', '_', str($read.element_identifier)) + #set $fn = "fw/" + $id + "_paired_" + str($i) + $extra + #silent $fw_fp.append( $fn ) +ln -s '$read' '$fn' && + #end for + #for $i, $read in enumerate($reads.read2) + #set $id = re.sub('[^\s\w\-\\.]', '_', str($read.element_identifier)) + #set $fn = "rv/" + $id + "_paired_" + str($i) + $extra + #silent $rv_fp.append( $fn ) +ln -s '$read' '$fn' && + #end for + #else if $reads.type == 'paired_collection' + #for $i, $read in enumerate($reads.paired_reads) + #set $id = re.sub('[^\s\w\-\\.]', '_', str($read.element_identifier)) + #set $fn = "fw/" + $id + "_paired_collection_" + str($i) + $extra + #silent $fw_fp.append( $fn ) +ln -s '$read.forward' '$fn' && + #set $fn = "rv/" + $id + "_paired_collection_" + str($i) + $extra + #silent $rv_fp.append( $fn ) +ln -s '$read.reverse' '$fn' && + #end for + #else if $reads.type == 'interleaved' + #for $i, $read in enumerate($reads.interleaved) + #set $id = re.sub('[^\s\w\-\\.]', '_', str($read.element_identifier)) + #set $fn = "interl/" + $id + "_interleaved_" + str($i) + $extra + #silent $interl_fp.append( $fn ) +ln -s '$read' '$fn' && + #end for + #end if + ]]></token> + <token name="@CO_ASSEMBLY_ALL_READS@"><![CDATA[ + #set $reads = $mapped.mode.read_type + #set $extra = '' + @CO_ASSEMBLY_READS@ + #for $j, $s in enumerate($mapped.mode.extra_reads) + #set $reads = $s.read_type + #set $extra = str($j) + @CO_ASSEMBLY_READS@ + #end for + ]]></token> + <token name="@CO_ASSEMBLY_REF@"><![CDATA[ + #for $i, $ref in enumerate($refs) + #set $fn = "ref/" + re.sub('[^\s\w\-\\.]', '_', str($ref.element_identifier)) + "_" + str($i) + #silent $ref_fp.append( $fn ) +ln -s '$ref' '${fn}' && + #end for + ]]></token> + <xml name="sharded"> + <param name="sharded" type="boolean" truevalue="--sharded" falsevalue="" checked="false" label="Input BAM files are read-sorted alignments of a set of reads mapped to multiple reference contig sets. Choose the best hit for each read pair. Otherwise if mapping was carried out: Map reads to each reference, choosing the best hit for each pair." /> </xml> <xml name="mapping"> - <section name="mapping" title="Mapping options" expanded="false"> - <param argument="--mapper" optional="true" type="select" label="Mapper" help="Underlying mapping software used. Default: minimap2-sr" > - <option value="minimap2-sr">minimap2 with '-x sr' option</option> - <option value="minimap2-ont">minimap2 with '-x map-ont' option</option> - <option value="minimap2-pb">minimap2 with '-x map-pb' option</option> - <option value="minimap2-no-preset">minimap2 with no '-x' option</option> - <option value="bwa-mem">BWA-MEM using default parameters</option> - </param> - <param argument="--min_read-aligned-length" type="integer" min="0" value="0" - label="Min read aligned length" help="Exclude reads with smaller numbers of aligned bases. Default: 0" /> - <param argument="--min_read-percent-identity" type="float" min="0" max="100" value="0" - label="Min read percent identity" help="Exclude reads by overall percent identity e.g. 95 for 95%. Default: 0" /> - <param argument="--min_read-aligned-percent" type="float" min="0" max="100" value="0" - label="Min read aligned percentage" help="Exclude reads by percent aligned bases e.g. 95 means 95% - of the read's bases must be aligned. Default: 0" /> - <param argument="--min_read-aligned-length-pair" type="integer" min="0" value="0" - label="Min read aligned length pair" help="Exclude pairs with smaller numbers of aligned bases. - Implies --proper-pairs-only. Default: 0" /> - <param argument="--min_read-percent-identity-pair" type="float" min="0" max="100" value="0" - label="Min read percent identity pair" help="Exclude pairs by overall percent identity e.g. 95 for 95%. - Implies --proper-pairs-only. Default: 0" /> - <param argument="--min_read-aligned-percent-pair" type="float" min="0" max="100" value="0" - label="Min read aligned percentage pair" help="Exclude reads by percent aligned bases e.g. 95 means 95% of - the read's bases must be aligned. Implies --proper-pairs-only. Default: 0" /> - <param argument="--proper-pairs-only" type="boolean" truevalue="--proper-pairs-only" falsevalue="" - label="Require reads to be mapped as proper pairs" help="Default: not set"/> - <param argument="--exclude-supplementary" type="boolean" truevalue="--exclude-supplementary" falsevalue="" - label="Exclude supplementary alignments" help="Default: not set"/> - </section> + <param argument="--mapper" type="select" label="Underlying mapping software used"> + <option value="minimap2-sr" selected="true">minimap2 with '-x sr' option</option> + <option value="minimap2-ont">minimap2 with '-x map-ont' option</option> + <option value="minimap2-pb">minimap2 with '-x map-pb' option</option> + <option value="minimap2-no-preset">minimap2 with no '-x' option</option> + <option value="bwa-mem">BWA-MEM using default parameters</option> + </param> </xml> - <xml name="coverage"> - <section name="cov" title="Coverage calculation options" expanded="false"> - <param name="relative_abundance" type="boolean" falsevalue="" truevalue="relative_abundance" label="Relative abundance (default)"/> - <param name="mean" type="boolean" falsevalue="" truevalue="mean" label="Mean"/> - <conditional name="cond_methods"> - <param name="trimmed_mean" type="select" label="Trimmed mean"> - <option value="trimmed_mean">Yes</option> + <xml name="alignment"> + <section name="alignment" title="Alignment thresholding" expanded="false"> + <param argument="--min-read-aligned-length" type="integer" min="0" value="0" + label="Minimum number of aligned bases" help="Reads with smaller numbers of aligned bases will be excluded" /> + <param argument="--min-read-percent-identity" type="float" min="0" max="100" value="0" + label="Minimum overall percent identity" help="Reads with lower overall percent identity will be excluded." /> + <param argument="--min-read-aligned-percent" type="float" min="0" max="100" value="0" + label="Minimum aligned base percent" help="Reads with lower percent aligned bases will be excluded" /> + <conditional name="proper_pairs_only"> + <param argument="--proper-pairs-only" type="select" label="Require reads to be mapped as proper pairs?"> + <option value="--proper-pairs-only">Yes</option> <option value="" selected="true">No</option> </param> - <when value="trimmed_mean"> - <param name="trim_min" type="integer" min="0" value="5" label="Trim min" help="Remove this smallest fraction of positions when calculating trimmed_mean default: 5"/> - <param name="trim_max" type="integer" min="0" value="95" label="Trim max" help="Maximum fraction for trimmed_mean calculations default: 95"/> + <when value="--proper-pairs-only"> + <param argument="--min_read-aligned-length-pair" type="integer" min="0" value="0" + label="Minimum number of aligned bases for pairs" help="Pairs with smaller numbers of aligned bases will be excluded." /> + <param argument="--min-read-percent-identity-pair" type="float" min="0" max="100" value="0" + label="Minimum overall percent identity pair for pairs" help="Pairs by lower overall percent identity will be excluded" /> + <param argument="--min-read-aligned-percent-pair" type="float" min="0" max="100" value="0" + label="Minimum percent of read aligned bases for pair" help="Pairs with lower reads percent aligned bases will be excluded" /> </when> <when value=""/> </conditional> - <param name="covered_bases" type="boolean" falsevalue="" truevalue="covered_bases" label="Covered bases"/> - <param name="covered_fraction" type="boolean" falsevalue="" truevalue="covered_fraction" label="Covered fraction"/> - <param name="variance" type="boolean" falsevalue="" truevalue="variance" label="Variance"/> - <param name="length" type="boolean" falsevalue="" truevalue="length" label="Length"/> - <param name="count" type="boolean" falsevalue="" truevalue="count" label="Count"/> - <param name="metabat" type="boolean" falsevalue="" truevalue="metabat" label="MetaBAT"/> - <param name="coverage_histogram" type="boolean" falsevalue="" truevalue="coverage_histogram" label="Coverage histogram"/> - <param name="reads_per_base" type="boolean" falsevalue="" truevalue="reads_per_base" label="Reads per base"/> - <param name="rpkm" type="boolean" falsevalue="" truevalue="rpkm" label="RPKM"/> - <param name="tpm" type="boolean" falsevalue="" truevalue="tpm" label="TPKM"/> - <param name="min_covered_fraction" type="integer" min="0" optional="true" - label="Min covered fraction" help="Genomes with less coverage than this reported as having zero coverage. Default: 10"/> - <param name="contig_end_exclusion" type="integer" min="0" optional="true" - label="Contig end exclusion" help="Exclude bases at the ends of reference sequences from calculation. Default: 75"/> + <param argument="--exclude-supplementary" type="boolean" truevalue="--exclude-supplementary" falsevalue="" checked="false" + label="Exclude supplementary alignments"/> </section> </xml> - <xml name="out"> - <section name="out" title="Output options" expanded="false"> - <param name="output_format" type="select" label="Shape of output" help="'Sparse' for long format, 'dense' for species-by-site. Default: dense]"> - <option value="dense" selected="true">Dense</option> - <option value="sparse">Sparse</option> - </param> - <param name="no_zeros" type="boolean" truevalue="--no-zeros" falsevalue="" optional="true" label="Omit printing of genomes that have zero coverage" /> - <param argument="--dereplication-output-cluster-definition" type="boolean" truevalue="--dereplication-output-cluster-definition" falsevalue="" label="Output a file of representative TAB member lines." /> - <param argument="--dereplication-output-representative-fasta-directory-copy" type="boolean" truevalue="--dereplication-output-representative-fasta-directory-copy" falsevalue="" label="Output representative genomes" /> - </section> + <xml name="cov_method_options"> + <option value="trimmed_mean">trimmed_mean: Average number of aligned reads overlapping each position after removing the most deeply and shallow-ly covered positions. </option> + <option value="coverage_histogram">coverage_histogram: Histogram of coverage depths</option> + <option value="covered_bases">covered_bases: Number of bases covered by 1 or more reads</option> + <option value="variance">variance: Variance of coverage depths</option> + <option value="length">length: Length of each contig in base pairs</option> + <option value="count">count: Number of reads aligned toq each contig. Note that a single read may be aligned to multiple contigs with supplementary alignments</option> + <option value="metabat">metabat: ("MetaBAT adjusted coverage") Coverage as defined in Kang et al 2015</option> + <option value="reads_per_base">reads_per_base: Number of reads aligned divided by the length of the contig</option> + <option value="rpkm">rpkm: Reads mapped per kilobase of contig, per million mapped reads</option> + <option value="tpm">tpm: Transcripts Per Million as described in Li et al 2010</option> + </xml> + <xml name="coverage_params"> + <param argument="--trim-min" type="integer" min="0" value="5" label="Smallest fraction of positions to remove when calculating" help="Only used with trimmed_mean method"/> + <param argument="--trim-max" type="integer" min="0" value="95" label="Maximum fraction of positions to remove when calculating" help="Only used with trimmed_mean method"/> + <param argument="--min-covered-fraction" type="integer" min="0" value="10" label="Minimum covered fraction" help="Genomes with less coverage than this reported as having zero coverage"/> + <param argument="--contig-end-exclusion" type="integer" min="0" value="75" label="Base to exclude at contig ends" help="Bases at the ends of reference sequences will be excluded from calculation"/> + </xml> + <xml name="output_format"> + <param argument="--output-format" type="select" label="Shape of output"> + <option value="dense" selected="true">Dense for species-by-site</option> + <option value="sparse">Sparse for long format</option> + </param> </xml> <xml name="citations"> <citations>