Mercurial > repos > thanhlv > polypolish
comparison polypolish.xml @ 0:3c7cbfb8f43d draft
"planemo upload for repository https://github.com/quadram-institute-bioscience/galaxy-tools/tree/master/tools/polypolish commit e855ff93b8b8493f8f061895d111885b938655e8-dirty"
author | thanhlv |
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date | Thu, 22 Sep 2022 13:42:49 +0000 |
parents | |
children | a38f6a0ebbf9 |
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-1:000000000000 | 0:3c7cbfb8f43d |
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1 <tool id="polypolish" name="polypolish" version="@VERSION@"> | |
2 <description> Polishing genome assemblies with short reads</description> | |
3 <macros> | |
4 <token name="@VERSION@">0.5.0</token> | |
5 </macros> | |
6 <requirements> | |
7 <requirement type="package" version="@VERSION@">polypolish</requirement> | |
8 <requirement type="package" version="1.15.1">samtools</requirement> | |
9 <requirement type="package" version="0.7.17">bwa</requirement> | |
10 </requirements> | |
11 <version_command>polypolish --version</version_command> | |
12 <command detect_errors="exit_code"><![CDATA[ | |
13 #if $short_reads.sr_type == 'paired' | |
14 ln -s '$short_read.R1' reads_1.fastq.gz && | |
15 ln -s '$short_read.R2' reads_2.fastq.gz && | |
16 #else if str($short_reads.sr_type) == "collection" | |
17 ln -s '$short_read.input1.forward' reads_1.fastq.gz && | |
18 ln -s '$short_read.input1.reverse' reads_2.fastq.gz && | |
19 #end if | |
20 | |
21 ln -s '${assembly}' draft.fa && | |
22 bwa index draft.fa && | |
23 bwa mem -t \${GALAXY_SLOTS:-4} -a draft.fa reads_1.fastq.gz > alignments_1.sam && | |
24 bwa mem -t \${GALAXY_SLOTS:-4} -a draft.fa reads_2.fastq.gz > alignments_2.sam && | |
25 polypolish_insert_filter.py --in1 alignments_1.sam --in2 alignments_2.sam --out1 filtered_1.sam --out2 filtered_2.sam && | |
26 polypolish | |
27 #if $debug | |
28 $debug debug.tsv | |
29 #end if | |
30 -d ${min_depth} | |
31 -i ${fraction_invalid} | |
32 -m ${max_errors} | |
33 -v ${fraction_valid} | |
34 draft.fasta filtered_1.sam filtered_2.sam | |
35 > polished.fasta | |
36 ]]> </command> | |
37 | |
38 <inputs> | |
39 <param name="basecalled" type="data" format="fastq,fastq.gz,fasta,fasta.gz" label="Basecalled data"/> | |
40 <conditional name="short_reads"> | |
41 <param name="sr_type" type="select" label="Input reads type or collection" help="Select 'paired end' for a single library or 'collection' for a paired end collection"> | |
42 <option value="paired" selected="true">Paired End</option> | |
43 <option value="collection">Paired Collection</option> | |
44 </param> | |
45 <when value="paired"> | |
46 <param name="R1" type="data" format="fastqsanger,fastqsanger.gz,fastqsanger.bz2" label="Forward reads (R1)" help="The file of forward reads in FASTQ format"/> | |
47 <param name="R2" type="data" format="fastqsanger,fastqsanger.gz,fastqsanger.bz2" label="Reverse reads (R2)" help="The file of reverse reads in FASTQ format"/> | |
48 </when> | |
49 <when value="collection"> | |
50 <param name="input1" format="fastqsanger,fastqsanger.gz,fastqsanger.bz2" type="data_collection" collection_type="paired" label="Paired collection" help="See help section for an explanation of dataset collections"/> | |
51 </when> | |
52 </conditional> | |
53 <param argument="min_depth" type="integer" value="5" min="1" label="Minimum depth" /> | |
54 <param argument="fraction_invalid" type="float" value="0.2" min="0.0" max="1.0" label="Fraction value of the read depth to be considered invalid" /> | |
55 <param argument="fraction_valid" type="integer" value="10" min="1" label="Ignore alignments with more than this many mismatches and indels" /> | |
56 <param argument="max_errors" type="integer" value="10" min="1" label="Fraction value of the read depth to be considered invalid" /> | |
57 <param argument="debug" type="boolean" truevalue="--debug" falsevalue="" checked="false" label="Debug output" /> | |
58 </inputs> | |
59 <outputs> | |
60 <data name="polished" format="fasta" from_work_dir="polished.fasta" label="${tool.name} on ${on_string} Polished assembly" /> | |
61 <data name="debug" format="tabular" from_work_dir="debug.tsv" label="${tool.name} on ${on_string} Polished assembly" > | |
62 <filter>debug is True</filter> | |
63 </data> | |
64 </outputs> | |
65 <help><![CDATA[ | |
66 ]]> </help> | |
67 </tool> |