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planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/seqkit commit 99c10c3df0424268179b3f54f89e01a34b9e120e
author | iuc |
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date | Sat, 18 May 2024 23:11:47 +0000 |
parents | 6510652376b1 |
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<tool id="seqkit_locate" name="SeqKit locate" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@" profile="@PROFILE@"> <description>subsequences/motifs, mismatch allowed</description> <macros> <import>macros.xml</import> </macros> <expand macro="bio_tools"/> <expand macro="requirements"/> <command detect_errors="exit_code"><![CDATA[ #import re #set input_identifier = re.sub('[^\s\w\-]', '_', str($input.element_identifier)) ln -s '${input}' '${input_identifier}' && seqkit locate --threads \${GALAXY_SLOTS:-4} #if $conditional_pattern.mode == 'expression' --pattern '"$conditional_pattern.pattern"' $conditional_pattern.use_regexp #else --pattern-file '$conditional_pattern.pattern_file' #end if $output_mode $advanced_options.circular $advanced_options.degenerate $advanced_options.hide_matched $advanced_options.ignore_case #if not $advanced_options.degenerate --max-mismatch $advanced_options.max_mismatch $advanced_options.use_fmi #end if $advanced_options.non_greedy $advanced_options.only_positive_strand $advanced_options.id_ncbi --seq-type $seq_type '${input_identifier}' > '$output' ]]></command> <inputs> <param name="input" type="data" format="fasta,fasta.gz" label="Input file"/> <conditional name="conditional_pattern"> <param name="mode" type="select" label="Pattern mode" help="Specify a pattern/motif sequence or a FASTA file with the motif of interest. Motifs could be EITHER plain sequence containing 'ACTGN' OR regular expression like 'A[TU]G(?:.{3})+?[TU](?:AG|AA|GA)' for ORFs"> <option value="expression">Pattern/motif sequence</option> <option value="file">FASTA file with the pattern/motif of interest</option> </param> <when value="expression"> <param argument="--pattern" type="text" value="" label="Pattern/motif sequence" help="Perl regular expressions are allowed"> <sanitizer invalid_char=""> <valid initial="string.letters,string.digits"> <add value="^"/> <add value="$"/> <add value="("/> <add value=")"/> <add value="|"/> <add value="?"/> <add value="*"/> <add value="+"/> <add value="{"/> <add value="}"/> <add value="\"/> <add value="["/> <add value="]"/> <add value="."/> <add value=","/> </valid> </sanitizer> <validator type="regex" message="Pattern must not end with backslash.">.*[^\\]$</validator> </param> <param argument="--use-regexp" type="boolean" truevalue="--use-regexp" falsevalue="" checked="false" label="Pattern/motifs are regular expressions"/> </when> <when value="file"> <param argument="--pattern-file" type="data" format="fasta" label="Pattern/motif file"/> </when> </conditional> <param argument="--seq-type" type="select" label="Sequence type" help="For automatic detection, it automatically detect by the first sequence. Default: auto"> <option value="auto">Automatic detection</option> <option value="dna">DNA</option> <option value="rna">RNA</option> <option value="protein">Protein</option> </param> <param name="output_mode" type="select" label="Output mode"> <option value="">Tabular (default format)</option> <option value="--gtf">GTF</option> <option value="--bed">BED6</option> </param> <section name="advanced_options" title="Advanced options"> <param argument="--circular" type="boolean" truevalue="--circular" falsevalue="" checked="false" label="Circular genome" help="When using flag --circular, end position of matched subsequence that crossing genome sequence end would be greater than sequence length"/> <param argument="--degenerate" type="boolean" truevalue="--degenerate" falsevalue="" checked="false" label="Pattern/motif contains degenerate bases" help="Do not use degenerate bases/residues in regular expression, you need convert them to regular expression, e.g., change 'N' or 'X' to '.'"/> <param argument="--hide-matched" type="boolean" truevalue="--hide-matched" falsevalue="" checked="false" label="Do not show matched sequences"/> <param argument="--ignore-case" type="boolean" truevalue="--ignore-case" falsevalue="" checked="false" label="Ignore case"/> <param argument="--max-mismatch" type="integer" min="0" value="0" label="Maximum mismatch" help="For large genomes like human genome, using mapping/alignment tools would be faster"/> <param argument="--non-greedy" type="boolean" truevalue="--non-greedy" falsevalue="" checked="false" label="Non-greedy mode" help="Faster, but muy miss motifs overlapping with others"/> <param argument="--only-positive-strand" type="boolean" truevalue="--only-positive-strand" falsevalue="" checked="false" label="Only search on positive strand"/> <param argument="--use-fmi" type="boolean" truevalue="--use-fmi" falsevalue="" checked="false" label="FM-index" help="Use FM-index for much faster search of lots of sequence patterns. This option is not compatible with the --degenerate option"/> <param argument="--id-ncbi" type="boolean" truevalue="--id-ncbi" falsevalue="" checked="false" label="FASTA head is NCBI stype" help="Example: >gi|110645304|ref|NC_002516.2| Pseud..."/> </section> </inputs> <outputs> <data name="output" format="tabular" label="${tool.name} on ${on_string}"> <change_format> <when input="output_mode" value="--gtf" format="gtf"/> <when input="output_mode" value="--bed" format="bed"/> </change_format> </data> </outputs> <tests> <test expect_num_outputs="1"> <param name="input" value="input1.fasta.gz" ftype="fasta.gz"/> <conditional name="conditional_pattern"> <param name="mode" value="expression"/> <param name="pattern" value="ATAGAT"/> </conditional> <section name="advanced_options"> <param name="max_mismatch" value="1"/> </section> <output name="output" file="locate_output1.tabular" ftype="tabular"/> </test> <test expect_num_outputs="1"> <param name="input" value="input1.fasta.gz" ftype="fasta.gz"/> <conditional name="conditional_pattern"> <param name="mode" value="expression"/> <param name="pattern" value="A[TU]G"/> <param name="use_regexp" value="true"/> </conditional> <param name="output_mode" value="--bed"/> <section name="advanced_options"> <param name="circular" value="true"/> <param name="hide_matched" value="true"/> <param name="ignore_case" value="true"/> <param name="only_positive_strand" value="true"/> <param name="id_ncbi" value="true"/> </section> <output name="output" file="locate_output2.bed" ftype="bed"/> </test> <test expect_num_outputs="1"> <param name="input" value="input1.fasta.gz" ftype="fasta.gz"/> <conditional name="conditional_pattern"> <param name="mode" value="file"/> <param name="pattern_file" value="motif_sequence.fasta"/> </conditional> <param name="output_mode" value="--gtf"/> <section name="advanced_options"> <param name="use_fmi" value="true"/> </section> <output name="output" file="locate_output3.gtf" ftype="gtf"/> </test> <test expect_num_outputs="1"> <param name="input" value="input1.fasta.gz" ftype="fasta.gz"/> <conditional name="conditional_pattern"> <param name="mode" value="expression"/> <param name="pattern" value="ATAGAT"/> </conditional> <param name="seq_type" value="dna"/> <section name="advanced_options"> <param name="max_mismatch" value="1"/> </section> <output name="output" file="locate_output1.tabular" ftype="tabular"/> </test> </tests> <help> .. class:: infomark **Purpose** Locate subsequences/motifs, mismatch allowed. ------ .. class:: infomark **Attention** 1. Motifs could be EITHER plain sequence containing "ACTGN" OR regular expression like "A[TU]G(?:.{3})+?[TU](?:AG|AA|GA)" for ORFs. 2. Degenerate bases/residues like "RYMM.." are also supported by flag -d. But do not use degenerate bases/residues in regular expression, you need convert them to regular expression, e.g., change "N" or "X" to ".". 3. When providing search patterns (motifs) via flag '-p', please use double quotation marks for patterns containing comma, e.g., -p '"A{2,}"' or -p "\"A{2,}\"". Because the command line argument parser accepts comma-separated-values (CSV) for multiple values (motifs). Patterns in file do not follow this rule. 4. Mismatch is allowed using flag "-m/--max-mismatch", you can increase the value of "-j/--threads" to accelerate processing. 5. When using flag --circular, end position of matched subsequence that crossing genome sequence end would be greater than sequence length. </help> <expand macro="citations"/> </tool>