Mercurial > repos > miller-lab > genome_diversity
annotate coverage_distributions.xml @ 5:8a1147101f85
added 3rd party software
author | Richard Burhans <burhans@bx.psu.edu> |
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date | Tue, 10 Apr 2012 12:49:47 -0400 |
parents | 7a94f11fe71f |
children | e29f4d801bb0 |
rev | line source |
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0 | 1 <tool id="gd_coverage_distributions" name="Coverage" version="1.0.0"> |
2 <description>distributions</description> | |
3 | |
4 <command interpreter="python"> | |
4
7a94f11fe71f
change output.extra_files_path to output.files_path
Richard Burhans <burhans@bx.psu.edu>
parents:
0
diff
changeset
|
5 coverage_distributions.py "$input" "0" "$output" "$output.files_path" |
0 | 6 #if $individuals.choice == '0' |
7 "all_individuals" | |
8 #else if $individuals.choice == '1' | |
9 #set $arg = 'individuals:%s' % str($individuals.p1_input) | |
10 "$arg" | |
11 #else if $individuals.choice == '2' | |
12 #for $population in $individuals.populations | |
13 #set $arg = 'population:%s:%s' % (str($population.p_input), str($population.p_input.name)) | |
14 "$arg" | |
15 #end for | |
16 #end if | |
17 #for $individual, $individual_col in zip($input.dataset.metadata.individual_names, $input.dataset.metadata.individual_columns) | |
18 #set $individual_arg = 'individual:%s:%s' % ($individual_col, $individual) | |
19 "$individual_arg" | |
20 #end for | |
21 </command> | |
22 | |
23 <inputs> | |
24 <param name="input" type="data" format="wsf" label="SNP table" /> | |
25 | |
26 <conditional name="individuals"> | |
27 <param name="choice" type="select" label="Individuals"> | |
28 <option value="0" selected="true">All</option> | |
29 <option value="1">Individuals in a population</option> | |
30 <option value="2">Population totals</option> | |
31 </param> | |
32 <when value="0" /> | |
33 <when value="1"> | |
34 <param name="p1_input" type="data" format="ind" label="Population individuals" /> | |
35 </when> | |
36 <when value="2"> | |
37 <repeat name="populations" title="Population" min="1"> | |
38 <param name="p_input" type="data" format="ind" label="individuals" /> | |
39 </repeat> | |
40 </when> | |
41 </conditional> | |
42 | |
43 <!-- | |
44 <param name="data_source" type="select" label="Data source"> | |
45 <option value="0" selected="true">Sequence coverage</option> | |
46 <option value="1">Genotype quality</option> | |
47 </param> | |
48 --> | |
49 </inputs> | |
50 | |
51 <outputs> | |
52 <data name="output" format="html" /> | |
53 </outputs> | |
54 | |
55 <tests> | |
56 <test> | |
57 <param name="input" value="test_in/sample.wsf" ftype="wsf" /> | |
58 <param name="choice" value="0" /> | |
59 <output name="output" file="test_out/coverage_distributions/coverage.html" ftype="html" compare="diff" lines_diff="2"> | |
60 <extra_files type="file" name="coverage.pdf" value="test_out/coverage_distributions/coverage.pdf" compare="sim_size" delta = "1000"/> | |
61 <extra_files type="file" name="coverage.txt" value="test_out/coverage_distributions/coverage.txt" /> | |
62 </output> | |
63 </test> | |
64 </tests> | |
65 | |
66 <help> | |
67 **What it does** | |
68 | |
69 This tool reports distributions of SNP reliability indicators for | |
70 individuals or populations. The reliability is measured by the sequence | |
71 coverage. Textual and graphical reports are generated, where the text | |
72 output gives the cumulative distributions. | |
73 </help> | |
74 </tool> | |
75 |