Mercurial > repos > devteam > vcfgeno2haplo
comparison vcfgeno2haplo.xml @ 0:74d4e986f488 draft
planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tool_collections/vcflib/vcfgeno2haplo commit 5a4e0ca9992af3a6e5ed2b533f04bb82ce761e0b
| author | devteam |
|---|---|
| date | Mon, 09 Nov 2015 12:32:31 -0500 |
| parents | |
| children | d731d6f785b5 |
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| -1:000000000000 | 0:74d4e986f488 |
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| 1 <tool id="vcfgeno2haplo" name="VCFgenotype-to-haplotype:" version="0.0.3"> | |
| 2 <description>Convert genotype-based phased alleles into haplotype alleles</description> | |
| 3 <macros> | |
| 4 <import>macros.xml</import> | |
| 5 </macros> | |
| 6 <expand macro="requirements"></expand> | |
| 7 <expand macro="stdio"></expand> | |
| 8 <command> | |
| 9 #set $reference_fasta_filename = "localref.fa" | |
| 10 #if str( $reference_source.reference_source_selector ) == "history": | |
| 11 ln -s "${reference_source.ref_file}" "${reference_fasta_filename}" && | |
| 12 #else: | |
| 13 #set $reference_fasta_filename = str( $reference_source.ref_file.fields.path ) | |
| 14 #end if | |
| 15 vcfgeno2haplo ${output_option} -w ${window_size} -r "${reference_fasta_filename}" "${input_vcf}" > "${out_file1}"</command> | |
| 16 <inputs> | |
| 17 <conditional name="reference_source"> | |
| 18 <param name="reference_source_selector" type="select" label="Choose the source for the reference genome"> | |
| 19 <option value="cached">Locally cached</option> | |
| 20 <option value="history">History</option> | |
| 21 </param> | |
| 22 <when value="cached"> | |
| 23 <param name="ref_file" type="select" label="Select reference genome"> | |
| 24 <options from_data_table="fasta_indexes"> | |
| 25 <!--<filter type="data_meta" key="dbkey" ref="input_bam" column="value"/>--> | |
| 26 </options> | |
| 27 <validator type="no_options" message="A built-in reference genome is not available for the build associated with the selected input file"/> | |
| 28 </param> | |
| 29 <param name="input_vcf" type="data" format="vcf" label="Select VCF dataset"> | |
| 30 <!-- Validators are commented to allow users apply too to any build. May need to be revised in the future | |
| 31 <validator type="unspecified_build" /> | |
| 32 <validator type="dataset_metadata_in_data_table" table_name="fasta_indexes" metadata_name="dbkey" metadata_column="1" message="Sequences are not currently available for the specified build." /> | |
| 33 --> | |
| 34 </param> | |
| 35 </when> | |
| 36 <when value="history"> <!-- FIX ME!!!! --> | |
| 37 <param name="ref_file" type="data" format="fasta" label="Using reference file" /> | |
| 38 <param name="input_vcf" type="data" format="vcf" label="Select VCF dataset" /> | |
| 39 </when> | |
| 40 </conditional> | |
| 41 <param name="window_size" type="text" value="30" label="compare records up to this many bp away" help="--window-size option (default = 30)" /> | |
| 42 <param name="output_option" type="boolean" truevalue="-o" falsevalue="" label="What to report?" help="--only-variants option" /> | |
| 43 <!-- <option value=" ">Output entire haplotype</option> | |
| 44 <option value="-o">Don't output the entire haplotype, just concatenate REF/ALT strings (delimited by ":")</option> | |
| 45 </param> --> | |
| 46 </inputs> | |
| 47 <outputs> | |
| 48 <data format="vcf" name="out_file1" /> | |
| 49 </outputs> | |
| 50 <tests> | |
| 51 <test> | |
| 52 <param name="reference_source_selector" value="history" /> | |
| 53 <param name="output_option" value="true" /> | |
| 54 <param name="window_size" value="5000" /> | |
| 55 <param name="input_vcf" value="vcflib-phix.vcf"/> | |
| 56 <param name="ref_file" value="vcflib-test-genome-phix.fa" /> | |
| 57 <output name="out_file1" file="vcfgeno2haplo-test1.vcf"/> | |
| 58 </test> | |
| 59 </tests> | |
| 60 <help> | |
| 61 | |
| 62 Convert genotype-based phased alleles within a window size specified by -w option into haplotype alleles. Will break haplotype construction when encountering non-phased genotypes on input. | |
| 63 | |
| 64 The options are:: | |
| 65 | |
| 66 -w, --window-size N Merge variants at most this many bp apart (default 30) | |
| 67 -o, --only-variants Don't output the entire haplotype, just concatenate | |
| 68 REF/ALT strings (delimited by ":") | |
| 69 | |
| 70 ---- | |
| 71 | |
| 72 Vcfgeno2haplo @IS_PART_OF_VCFLIB@ | |
| 73 </help> | |
| 74 <expand macro="citations" /> | |
| 75 </tool> |
