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planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/main/tools/fastga commit 6504da2141da78f7cadb90a2a00e8744b1e0377a
| author | iuc |
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| date | Fri, 20 Feb 2026 07:47:05 +0000 |
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<tool id="fastga" name="FastGA" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@" profile="@PROFILE@"> <description>align whole genomes</description> <macros> <import>fastga_macros.xml</import> </macros> <expand macro="requirements" /> <command detect_errors="exit_code"><![CDATA[ ## FastGA directly string matches the file extensions ## symlinks are used to bypass that restriction ln -s '$input1' 'input1.${input1.ext}' && ln -s '$input2' 'input2.${input2.ext}' && FastGA '${output_settings.out.format}' #if str( $output_settings.out.format ) == "-paf": #if str( $output_settings.out.cigar_string ) != "no": '${output_settings.out.cigar_string}' #end if #if str( $output_settings.out.cs_string ) != "no": '${output_settings.out.cs_string}' #end if #end if $use_soft_mask $use_sym_seeding -f${adaptive_seed_count_cutoff} -c${minimum_seed_coverage} -s${new_seed_threshold} -l${minimum_alignment_length} -i${minimum_alignment_identity} 'input1.${input1.ext}' 'input2.${input2.ext}' #if str( $output_settings.out.format ) != "-1:output": > output #end if ]]></command> <inputs> <param name="input1" type="data" label="FASTA sequence" format="fasta,fasta.gz"/> <param name="input2" type="data" label="FASTA sequence" format="fasta,fasta.gz"/> <param name="use_soft_mask" type="boolean" label="Use soft mask information if available (-M)" checked="false" truevalue="-M" falsevalue=""/> <param name="use_sym_seeding" type="boolean" label="Use symmetric seeding (-S)" checked="false" truevalue="-S" falsevalue=""/> <param name="adaptive_seed_count_cutoff" type="integer" label="Adaptive seed count cutoff (-f)" value="10" min="0" max="255"/> <param name="minimum_seed_coverage" type="integer" label="Minimum seed chain coverage in both genomes (-c)" value="85" min="0"/> <param name="new_seed_threshold" type="integer" label="Threshold for starting a new seed chain (-s)" value="1000" min="0"/> <param name="minimum_alignment_length" type="integer" label="Minimum alignment length (-l)" value="100" min="0"/> <param name="minimum_alignment_identity" type="float" label="Minimum alignment identity (-i)" value="0.7" min="0.55" max="0.99999999999999994"/> <section name="output_settings" expanded="False" title="Output"> <conditional name="out"> <param name="format" type="select" label="Specify the output format"> <option value="-paf" selected="true">paf (-paf)</option> <option value="-psl">psl (-psl)</option> <option value="-1:output">1aln (-1)</option> </param> <when value="-paf"> <param name="cigar_string" type="select" label="Use CIGAR string?"> <option value="no" selected="true">No CIGAR string</option> <option value="-pafx">CIGAR string with X's (-pafx)</option> <option value="-pafm">CIGAR string with ='s (-pafm)</option> </param> <param name="cs_string" type="select" label="Use CS string?"> <option value="no" selected="true">No CS string</option> <option value="-pafs">CS string in short form (-pafs)</option> <option value="-pafS">CS string in long form (-pafS)</option> </param> </when> <when value="-psl"/> <when value="-1:output"/> </conditional> </section> </inputs> <outputs> <data name="output" format="paf" from_work_dir="output"> <change_format> <when input="output_settings.out.format" value="-paf" format="paf"/> <when input="output_settings.out.format" value="-psl" format="psl"/> <when input="output_settings.out.format" value="-1:output" format="txt"/> </change_format> </data> </outputs> <tests> <test expect_num_outputs="1"> <param name="input1" value="chrM_hg38.fa.gz"/> <param name="input2" value="chrM_mm39.fa.gz"/> <section name="output_settings"> <conditional name="out"> <param name="format" value="-paf"/> </conditional> </section> <output name="output" file="chrM_HGvMM.paf" ftype="paf"/> </test> <test expect_num_outputs="1"> <param name="input1" value="chrM_hg38.fa.gz"/> <param name="input2" value="chrM_mm39.fa.gz"/> <section name="output_settings"> <conditional name="out"> <param name="format" value="-psl"/> </conditional> </section> <output name="output" file="chrM_HGvMM.psl" ftype="psl"/> </test> <test expect_num_outputs="1"> <param name="input1" value="chrM_hg38.fa.gz"/> <param name="input2" value="chrM_mm39.fa.gz"/> <section name="output_settings"> <conditional name="out"> <param name="format" value="-paf"/> <param name="cigar_string" value="-pafx"/> </conditional> </section> <output name="output" file="pafx.paf" ftype="paf"/> </test> <test expect_num_outputs="1"> <param name="input1" value="chrM_hg38.fa.gz"/> <param name="input2" value="chrM_mm39.fa.gz"/> <param name="use_soft_mask" value="True"/> <param name="use_sym_seeding" value="True"/> <param name="adaptive_seed_count_cutoff" value="9"/> <param name="minimum_seed_coverage" value="100"/> <param name="new_seed_threshold" value="750"/> <param name="minimum_alignment_length" value="90"/> <param name="minimum_alignment_identity" value="0.6"/> <section name="output_settings"> <conditional name="out"> <param name="format" value="-paf"/> <param name="cigar_string" value="-pafm"/> <param name="cs_string" value="-pafS"/> </conditional> </section> <output name="output" file="pafmS_options.paf" ftype="paf"/> </test> <test expect_num_outputs="1"> <param name="input1" value="chrM_hg38.fa.gz"/> <param name="input2" value="chrM_mm39.fa.gz"/> <section name="output_settings"> <conditional name="out"> <param name="format" value="-1:output"/> </conditional> </section> </test> </tests> <help><![CDATA[ FastGA compares two high-quality genomes and outputs a ``.1aln``, ``.paf``, or ``.psl`` file containing all local alignments found. It is based on a novel adaptive seed finding algorithm as well as the first wave-based local aligner developed for daligner (2012). FastGA uses a number of temporary, hidden files such as ONEcode genome databases (.1gdb) and genome indices (.gix) to achieve its high speed and space efficiency. ----- Input ***** This tool takes two ``fasta`` or ``fasta.gz`` input files to align. It is a core assumption of FastGA that the input genomes are nearly complete and are of high quality (Q40 or better). FastGA is not commutative by default (see *Use symmetric seeding* below). ----- Options ******* =============================== ======== =========== =========================== **Option** **Flag** **Default** **Description** ------------------------------- -------- ----------- --------------------------- Use soft mask information -M False Use soft-masked regions if present in the input FASTA Use symmetric seeding -S False Enables symmetric seeding (not recommended) Adaptive seed count cutoff -f 10 Range: 0–255 Minimum seed chain coverage -c 85 Range: ≥ 0 Threshold for new seed chain -s 1000 Range: ≥ 0 Minimum alignment length -l 100 Range: ≥ 0 Minimum alignment identity -i 0.7 Range: 0.55–<1.0 =============================== ======== =========== =========================== ----- Output ****** **Output format** ========== ======== =========== =============================== **Format** **Flag** **Default** **Notes** ---------- -------- ----------- ------------------------------- PAF -paf Yes PSL -psl No 1ALN -1 No Output is nondeterministic ========== ======== =========== =============================== **CIGAR string options** (available only when output format is PAF) ============================== ======== =========== **Option** **Flag** **Default** ------------------------------ -------- ----------- No CIGAR string Yes CIGAR string with X's -pafx No CIGAR string with ='s -pafm No ============================== ======== =========== **CS string options** (available only when output format is PAF) ============================== ======== =========== **Option** **Flag** **Default** ------------------------------ -------- ----------- No CS string Yes CS string (short form) -pafs No CS string (long form) -pafS No ============================== ======== =========== ]]></help> <expand macro="citations" /> </tool>
