Mercurial > repos > iuc > amas_concat
view amas_concat.xml @ 0:fb24e1904d08 draft default tip
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/main/tools/amas commit 158ec0e635067d354c425baf14b95cb616fd93c4
| author | iuc |
|---|---|
| date | Tue, 02 Dec 2025 09:26:01 +0000 |
| parents | |
| children |
line wrap: on
line source
<tool id="amas_concat" name="AMAS concat" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@" profile="@PROFILE@"> <description>concatenate multiple alignments</description> <macros> <import>macros.xml</import> </macros> <xrefs> <xref type="bio.tools">amas</xref> </xrefs> <expand macro="requirements" /> <expand macro="version_command" /> <command detect_errors="exit_code"><![CDATA[ #import re set -eu; @SNIFF_INPUT_FORMAT@ @CHECK_INTERLEAVED@ @SYMLINK_INPUTS@ python -m amas.AMAS concat --concat-part partitions.txt --concat-out concatenated.out --part-format $part_format --out-format $out_format --in-files @INPUT_FILENAMES@ --in-format "\${IN_FORMAT}" --data-type $data_type --cores "\${GALAXY_SLOTS:-1}" $check_align ]]></command> <inputs> <param name="input_files" type="data" format="fasta,phylip,nex" label="Sequences to concatenate" multiple="true" help="Provide pre-aligned FASTA/PHYLIP/NEXUS files (DNA or protein); mixes of unaligned reads or contigs will produce meaningless results." /> <expand macro="output_format" label="Select output format for concatenated alignment" /> <param name="part_format" type="select" label="Format of the partitions file" help="A file defining how the concatenated alignment is split into separate gene/locus regions. Each line specifies a partition name and its position range (e.g., 'gene1 = 1-500' or 'DNA, gene1 = 1-500' for RAxML format)."> <option value="unspecified" selected="true">unspecified</option> <option value="nexus">nexus</option> <option value="raxml">raxml</option> </param> <expand macro="data_type" /> <expand macro="check_align" /> </inputs> <outputs> <data name="output" from_work_dir="concatenated.out" format="txt" label="${tool.name} on ${on_string}: Concatenated alignment"> <change_format> <when input="out_format" value="fasta" format="fasta" /> <when input="out_format" value="phylip" format="phylip" /> <when input="out_format" value="phylip-int" format="phylip" /> <when input="out_format" value="nexus" format="nex" /> <when input="out_format" value="nexus-int" format="nex" /> </change_format> </data> <data name="partitions_out" from_work_dir="partitions.txt" format="txt" label="${tool.name} on ${on_string}: Partition file"> <change_format> <!-- Untitled and RAxML partition formats have no current equivalent datatypes so are outputted as txt by default --> <when input="part_format" value="nexus" format="nex" /> </change_format> </data> </outputs> <tests> <test expect_num_outputs="2"> <param name="input_files" value="inputs/concat_1.fasta,inputs/concat_2.fasta" /> <param name="out_format" value="phylip" /> <param name="part_format" value="nexus" /> <param name="data_type" value="dna" /> <param name="check_align" value="false" /> <output name="output" file="outputs/expected_concat.phylip" ftype="phylip" /> <output name="partitions_out" file="outputs/expected_partitions.nex" ftype="nex" /> </test> <test expect_num_outputs="2"> <param name="input_files" value="inputs/concat_1.fasta,inputs/concat_2.fasta" /> <param name="out_format" value="fasta" /> <param name="part_format" value="raxml" /> <param name="data_type" value="dna" /> <param name="check_align" value="false" /> <output name="output" file="outputs/expected_concat_fasta.fas" ftype="fasta" /> <output name="partitions_out" file="outputs/expected_partitions_raxml.txt" ftype="txt" /> </test> <!-- Interleave tests: amas starts interleaving when sequences have lines > 500 characters --> <test expect_num_outputs="2"> <param name="input_files" value="inputs/concat_int_1.phylip,inputs/concat_int_2.phylip" /> <param name="out_format" value="nexus-int" /> <param name="part_format" value="unspecified" /> <param name="data_type" value="dna" /> <param name="check_align" value="false" /> <output name="output" file="outputs/expected_concat_int.nex" ftype="nex" /> <output name="partitions_out" file="outputs/expected_partitions_int.txt" ftype="txt" /> </test> <!-- Nexus interleave tests for: 'INTERLEAVE', 'Interleave=yes;', no interleave flag --> <test expect_num_outputs="2"> <param name="input_files" value="inputs/concat_int_1.nex,inputs/concat_int_2.nex,inputs/concat_int_3.nex" /> <param name="out_format" value="nexus-int" /> <param name="part_format" value="unspecified" /> <param name="data_type" value="dna" /> <param name="check_align" value="false" /> <output name="output" file="outputs/expected_concat_int_multi.nex" ftype="nex" /> <output name="partitions_out" file="outputs/expected_partitions_int_multi.txt" ftype="txt" /> </test> </tests> <help><![CDATA[ **What it does** AMAS Concat combines multiple sequence alignments into a single concatenated alignment, commonly used in phylogenomic analyses. **Inputs** - **Multiple alignment files**: Select 2 or more pre-aligned sequence files (FASTA, PHYLIP, or NEXUS format) - **Input format**: Specify the format of your input files - **Partition format**: Specify how you want the partition file to be formatted (Unspecified, RAxML, NEXUS) - **Data type**: Choose DNA for nucleotide sequences or Protein for amino acid sequences - **Output format**: Select the desired format for the concatenated alignment **Outputs** 1. **Concatenated alignment**: A single file containing all input alignments joined end-to-end 2. **Partitions file**: Defines the boundaries of each original alignment within the concatenated file @PARTITIONS_HELP@ **Use cases** - **Multi-locus phylogenomics**: Combine hundreds of genes for species tree inference - **Partitioned phylogenetic analysis**: Apply different evolutionary models to different genes using tools like RAxML or IQ-TREE - **Supermatrix construction**: Create dataset for concatenation-based phylogenetic methods - **Increased phylogenetic signal**: Leverage information from multiple loci to resolve difficult nodes - **Comparative analyses**: Prepare datasets for testing hypotheses across multiple genomic regions @AMAS_SHARED_HELP@ ]]></help> <expand macro="citations" /> </tool>
