Mercurial > repos > peterjc > mira4_assembler
annotate tools/mira4/mira4_bait.xml @ 20:aeb3e35f8236 draft
Uploaded v0.0.4 preview, made MAF and BAM output optional
author | peterjc |
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date | Tue, 10 Jun 2014 10:11:58 -0400 |
parents | 8487d70e82aa |
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rev | line source |
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19 | 1 <tool id="mira_4_0_bait" name="MIRA v4.0 mirabait" version="0.0.3"> |
9 | 2 <description>Filter reads using kmer matches</description> |
3 <requirements> | |
4 <requirement type="binary">mirabait</requirement> | |
5 <requirement type="package" version="4.0">MIRA</requirement> | |
6 </requirements> | |
7 <version_command interpreter="python">mira4_bait.py --version</version_command> | |
8 <command interpreter="python"> | |
9 mira4_bait.py $input_reads.ext $output_choice $strand_choice $kmer_length $min_occurence "$bait_file" "$input_reads" "$output_reads" | |
10 </command> | |
11 <stdio> | |
12 <!-- Assume anything other than zero is an error --> | |
13 <exit_code range="1:" /> | |
14 <exit_code range=":-1" /> | |
15 </stdio> | |
16 <inputs> | |
15 | 17 <param name="bait_file" type="data" format="fasta,fastq,mira" required="true" label="Bait file (what to look for)" /> |
18 <param name="input_reads" type="data" format="fasta,fastq,mira" required="true" label="Reads to search" /> | |
9 | 19 <param name="output_choice" type="select" label="Output positive matches, or negative matches?"> |
20 <option value="pos">Just positive matches</option> | |
21 <option value="neg">Just negative matches</option> | |
22 </param> | |
23 <param name="strand_choice" type="select" label="Check for matches on both strands?"> | |
24 <option value="both">Check both strands</option> | |
25 <option value="fwd">Just forward strand</option> | |
26 </param> | |
15 | 27 <param name="kmer_length" type="integer" value="31" min="1" max="32" |
28 label="k-mer length" help="Maximum 32" /> | |
29 <param name="min_occurence" type="integer" value="1" min="1" | |
30 label="Minimum k-mer occurence" | |
31 help="How many k-mer matches do you want per read? Minimum one" /> | |
9 | 32 </inputs> |
33 <outputs> | |
18
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34 <data name="output_reads" format="input" metadata_source="input_reads" |
381aa262c8cb
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peterjc
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35 label="$input_reads.name #if str($output_choice)=='pos' then 'matching' else 'excluding matches to' # $bait_file.name"/> |
9 | 36 </outputs> |
37 <tests> | |
38 <test> | |
39 <param name="bait_file" value="tvc_bait.fasta" ftype="fasta" /> | |
40 <param name="input_reads" value="tvc_mini.fastq" ftype="fastqsanger" /> | |
41 <output name="output_reads" file="tvc_mini_bait_pos.fastq" ftype="fastqsanger" /> | |
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42 </test> |
9 | 43 <test> |
44 <param name="bait_file" value="tvc_bait.fasta" ftype="fasta" /> | |
45 <param name="input_reads" value="tvc_mini.fastq" ftype="fastqsanger" /> | |
46 <param name="kmer_length" value="32" /> | |
47 <param name="min_occurence" value="50" /> | |
48 <output name="output_reads" file="tvc_mini_bait_strict.fastq" ftype="fastqsanger" /> | |
49 </test> | |
50 <test> | |
51 <param name="bait_file" value="tvc_bait.fasta" ftype="fasta" /> | |
52 <param name="input_reads" value="tvc_mini.fastq" ftype="fastqsanger" /> | |
53 <param name="output_choice" value="neg" /> | |
54 <output name="output_reads" file="tvc_mini_bait_neg.fastq" ftype="fastqsanger" /> | |
55 </test> | |
56 </tests> | |
57 <help> | |
58 **What it does** | |
59 | |
60 Runs the ``mirabait`` utility from MIRA v4.0 to filter your input reads | |
61 according to whether or not they contain perfect kmer matches to your | |
62 bait file. By default this looks for 31-mers (kmers or *k*-mers where | |
63 the fragment length *k* is 31), and only requires a single matching kmer. | |
64 | |
65 The ``mirabait`` utility is useful in many applications and pipelines | |
66 outside of using the main MIRA tool for assembly or mapping. | |
67 | |
68 .. class:: warningmark | |
69 | |
70 Note ``mirabait`` cannot be used on protein (amino acid) sequences. | |
71 | |
72 **Example Usage** | |
73 | |
74 To remove over abundant entries like rRNA sequences, run ``mirabait`` with | |
75 known rRNA sequences as the bait and select the *negative* matches. | |
76 | |
77 To do targeted assembly by fishing out reads belonging to a gene and just | |
78 assemble these, run ``mirabait`` with the gene of interest as the bait and | |
79 select the *positive* matches. | |
80 | |
81 To iteratively reconstruct mitochondria you could start by fishing out reads | |
82 matching any known mitochondrial sequence, assembly those, and repeat. | |
83 | |
84 | |
85 **Notes on paired read** | |
86 | |
87 .. class:: warningmark | |
88 | |
89 While MIRA4 is aware of many read naming conventions to identify paired read | |
90 partners, the ``mirabait`` tool considers each read in isolation. Applying | |
91 it to paired read files may leave you with orphaned reads. | |
92 | |
93 | |
94 **Citation** | |
95 | |
96 If you use this Galaxy tool in work leading to a scientific publication please | |
97 cite the following papers: | |
98 | |
99 Peter J.A. Cock, Björn A. Grüning, Konrad Paszkiewicz and Leighton Pritchard (2013). | |
100 Galaxy tools and workflows for sequence analysis with applications | |
101 in molecular plant pathology. PeerJ 1:e167 | |
102 http://dx.doi.org/10.7717/peerj.167 | |
103 | |
104 Bastien Chevreux, Thomas Wetter and Sándor Suhai (1999). | |
105 Genome Sequence Assembly Using Trace Signals and Additional Sequence Information. | |
106 Computer Science and Biology: Proceedings of the German Conference on Bioinformatics (GCB) 99, pp. 45-56. | |
107 http://www.bioinfo.de/isb/gcb99/talks/chevreux/main.html | |
108 | |
109 This wrapper is available to install into other Galaxy Instances via the Galaxy | |
110 Tool Shed at http://toolshed.g2.bx.psu.edu/view/peterjc/mira4_assembler | |
111 </help> | |
112 </tool> |