comparison test-data/microsatcompat.xml @ 4:ecfc9041bcc5

Deleted selected files
author arkarachai-fungtammasan
date Wed, 01 Apr 2015 14:05:54 -0400
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1 <tool id="microsatcompat" name="Check microsatellites motif compatibility" version="1.0.0">
2 <description> </description>
3 <command interpreter="python">microsatcompat.py $input $column1 $column2 > $output </command>
4
5 <inputs>
6 <param name="input" type="data" label="Select input" />
7 <param name="column1" type="integer" value="4" label="First column number" />
8 <param name="column2" type="integer" value="10" label="Second column number" />
9 </inputs>
10 <outputs>
11 <data format="tabular" name="output" />
12
13 </outputs>
14 <tests>
15 <!-- Test data with valid values -->
16 <test>
17 <param name="input" value="microsatcompat_in.txt"/>
18 <param name="column1" value="4"/>
19 <param name="column2" value="10"/>
20 <output name="output" file="microsatcompat_out.txt"/>
21 </test>
22
23 </tests>
24 <help>
25
26
27 .. class:: infomark
28
29 **What it does**
30
31 This tool is used to select only the input lines which have compatible microsatellite motifs between two columns. Compatible here is defined as the microsatellites motif that are complementary or have the same sequence when change starting point of motif. For example, **A** is the same as **T**. Also, **AGG** is the same as **GAG**.
32
33 For TRFM pipeline (profiling microsatellites in short read data), this tool can be used to make sure that the microsatellites in the reads have the same motif as the microsatellites in the reference at the corresponding mapped location.
34
35 **Citation**
36
37 When you use this tool, please cite **Fungtammasan A, Ananda G, Hile SE, Su MS, Sun C, Harris R, Medvedev P, Eckert K, Makova KD. 2015. Accurate Typing of Short Tandem Repeats from Genome-wide Sequencing Data and its Applications, Genome Research**
38
39 **Input**
40
41 The input files can be any tab delimited file.
42
43 If this tool is used in TRFM microsatellite profiling, it should contains:
44
45 - Column 1 = microsatellite location in reference chromosome
46 - Column 2 = microsatellite location in reference start
47 - Column 3 = microsatellite location in reference stop
48 - Column 4 = microsatellite location in reference motif
49 - Column 5 = microsatellite location in reference length
50 - Column 6 = microsatellite location in reference motif size
51 - Column 7 = length of microsatellites (bp)
52 - Column 8 = length of left flanking regions (bp)
53 - Column 9 = length of right flanking regions (bp)
54 - Column 10 = repeat motif (bp)
55 - Column 11 = hamming distance
56 - Column 12 = read name
57 - Column 13 = read sequence with soft masking of microsatellites
58 - Column 14 = read quality (the same Phred score scale as input)
59 - Column 15 = read name (The same as column 12)
60 - Column 16 = chromosome
61 - Column 17 = left flanking region start
62 - Column 18 = left flanking region stop
63 - Column 19 = microsatellite start as infer from pair-end
64 - Column 20 = microsatellite stop as infer from pair-end
65 - Column 21 = right flanking region start
66 - Column 22 = right flanking region stop
67 - Column 23 = microsatellite length in reference
68 - Column 24 = microsatellite sequence in reference
69
70 **Output**
71
72 The same as input format.
73
74
75 </help>
76 </tool>