Mercurial > repos > cmonjeau > discosnp_plus_plus
comparison bbric_disco.xml @ 0:1beb3ed9e1e3
Imported from capsule None
author | cmonjeau |
---|---|
date | Fri, 05 Jun 2015 11:40:18 -0400 |
parents | |
children |
comparison
equal
deleted
inserted
replaced
-1:000000000000 | 0:1beb3ed9e1e3 |
---|---|
1 <tool id="discosnp_pp" name="discoSnp++" version="2.1.7"> | |
2 <description>is an efficient tool for detecting SNPs without a reference genome.</description> | |
3 <requirements> | |
4 <requirement type="package" version="2.1.7">discoSnp_plus_plus</requirement> | |
5 <requirement type="package" version="0.6.2">bwa</requirement> | |
6 </requirements> | |
7 <command interpreter="python"> | |
8 bbric_disco.py | |
9 -r ${datfile} | |
10 -b $branching_bubbles | |
11 -D $deletions | |
12 -P $limit_snp | |
13 #if $low_complexity | |
14 -l | |
15 #end if | |
16 -k $kmer | |
17 #if (str($extension) == 't'): | |
18 -t | |
19 #end if | |
20 #if (str($extension) == 'T'): | |
21 -T | |
22 #end if | |
23 -c $coverage | |
24 -C ${maxcoverage} | |
25 -d $error_threshold | |
26 #if (str($VCF_option.mapping) == 'reference'): | |
27 -G ${VCF_option.reference} | |
28 -M ${VCF_option.mapping_error} | |
29 #end if | |
30 </command> | |
31 | |
32 <inputs> | |
33 <repeat name="input_list" title="input files" min="1"> | |
34 <param name="input" type="data" format="fasta,fastq,fastq.gz" label="input"/> | |
35 </repeat> | |
36 | |
37 <param name="kmer" type="integer" label="Size of kmers" value="31" /> | |
38 <param name="coverage" type="integer" label="Minimal coverage per read set" value="4" /> | |
39 <param name="maxcoverage" type="integer" label="Maximal coverage per read set" value="2147483647" help="default value = 2^31-1" /> | |
40 <param name="error_threshold" type="integer" label="Max number of errors per read" value="1" help="Max number of errors per read" /> | |
41 | |
42 <param name="branching_bubbles" type="select" label="branching strategy"> | |
43 <option value="0">variants for which any of the two paths is branching are discarded</option> | |
44 <option value="1">forbid SNPs for wich the two paths are branching</option> | |
45 <option value="2">No limitation on branching</option> | |
46 </param> | |
47 | |
48 <param name="deletions" type="integer" label="deletion size" value="0" help="If different of 0, discoSnp++ will search for deletions of size from 1 to the value included"/> | |
49 <param name="limit_snp" type="integer" label="maximum SNPs per bubble" value="1" help="discoSnp++ will search up to the value SNPs in a unique bubble"/> | |
50 <param name="low_complexity" type="boolean" default="False" checked="False" label="accept low complexity bubbles" /> | |
51 | |
52 <param name="extension" type="select" label="extension strategy"> | |
53 <option value="n">extends to 30bp on left and right</option> | |
54 <option value="t">extends left and right until a polymorphism s found (unitigs)</option> | |
55 <option value="T">extends left and right using local assembly (contigs)</option> | |
56 </param> | |
57 <conditional name="VCF_option" > | |
58 <param name="mapping" type="select" label="VCF option"> | |
59 <option value="default">Do not use reference genome</option> | |
60 <option value="reference">Mapping with a reference genome</option> | |
61 </param> | |
62 <when value="defaut"></when> | |
63 <when value="reference"> | |
64 <param name="reference" type="data" format="fasta,fastq" label="Reference genome file" /> | |
65 <param name="mapping_error" type="integer" value="4" label="Maximal number of mapping errors" help="during BWA mapping phase" /> | |
66 </when> | |
67 </conditional> | |
68 | |
69 </inputs> | |
70 | |
71 <outputs> | |
72 <!-- <data name="report" from_work_dir="report.txt" format="txt" label="Output of ${tool.name} on $on_string"/> --> | |
73 <data name="vcf" from_work_dir="coherent.vcf" format="vcf" label="VCF of ${tool.name} on $on_string"/> | |
74 <data name="fasta" from_work_dir="coherent.fasta" format="fasta" label="Multifasta of the polymorphisms - ${tool.name} on $on_string"/> | |
75 </outputs> | |
76 | |
77 <configfiles> | |
78 <configfile name="datfile"> | |
79 #for $i, $lib in enumerate ($input_list) | |
80 ${i}::${lib.input} | |
81 #end for | |
82 </configfile> | |
83 </configfiles> | |
84 <help> | |
85 | |
86 **Description** | |
87 | |
88 Software discoSnp is designed for discovering Single Nucleotide Polymorphism (SNP) from raw set(s) of reads obtained with Next Generation Sequencers (NGS). | |
89 Note that number of input read sets is not constrained, it can be one, two, or more. Note also that no other data as reference genome or annotations are needed. | |
90 The software is composed by two modules. First module, kissnp2, detects SNPs from read sets. A second module, kissreads, enhance the kissnp2 results by computing per read set and for each found SNP i/ its mean read coverage and ii/ the (phred) quality of reads generating the polymorphism. | |
91 | |
92 Note that from release of DiscoSnp++-2.0.6, the tool also detects close SNPs and indels. | |
93 | |
94 ------- | |
95 | |
96 .. class:: warningmark | |
97 | |
98 **Input parameters** | |
99 | |
100 -Sequences files in fasta, fastq or fastq.gz, each allele will be counted in each file individually | |
101 | |
102 -Fasta sequence of a genome if case of you are willing to map the sequence extension on a reference in order to get a compliant VCF | |
103 | |
104 ------- | |
105 | |
106 .. class:: warningmark | |
107 | |
108 **Ouput parameters** | |
109 | |
110 -VCF file with coordinates on the higher branch sequences or on a reference genome if provided | |
111 | |
112 -Fasta file with sequence extensions around the SNP. | |
113 | |
114 | |
115 ------- | |
116 | |
117 **Web site** | |
118 | |
119 https://colibread.inria.fr/software/discosnp/ | |
120 | |
121 ------- | |
122 | |
123 **Integrated by** | |
124 | |
125 Cyril Monjeaud and Fabrice Legeai | |
126 | |
127 GenOuest Bio-informatics Core Facility | |
128 | |
129 UMR 6074 IRISA INRIA-CNRS-UR1 Rennes (France) | |
130 | |
131 support@genouest.org | |
132 | |
133 If you use this tool in Galaxy, please cite : | |
134 | |
135 `Y. Le Bras, A. Roult, C. Monjeaud, M. Bahin, O. Quenez, C. Heriveau, A. Bretaudeau, O. Sallou, O. Collin, Towards a Life Sciences Virtual Research Environment : an e-Science initiative in Western France. JOBIM 2013. <https://www.e-biogenouest.org/resources/128>`_ | |
136 | |
137 </help> | |
138 <citations> | |
139 <citation type="doi">10.1093/nar/gku1187</citation> | |
140 <citation type="bibtex">@INPROCEEDINGS{JOBIM2013, | |
141 author = {Le Bras, Y. and ROULT, A. and Monjeaud, C. and Bahin, M. and Quenez, O. and Heriveau, C. and Bretaudeau, A. and Sallou, O. and Collin, O.}, | |
142 title = {Towards a Life Sciences Virtual Research Environment: An e-Science initiative in Western France}, | |
143 booktitle = {JOBIM 2013 Proceedings}, | |
144 year = {2013}, | |
145 url = {https://www.e-biogenouest.org/resources/128}, | |
146 pages = {97-106} | |
147 } | |
148 </citation> | |
149 </citations> | |
150 </tool> | |
151 |