Mercurial > repos > miller-lab > genome_diversity
comparison average_fst.xml @ 14:8ae67e9fb6ff
Uploaded Miller Lab Devshed version a51c894f5bed again [possible toolshed.g2 bug]
author | miller-lab |
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date | Fri, 28 Sep 2012 11:35:56 -0400 |
parents | |
children | f04f40a36cc8 |
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13:fdb4240fb565 | 14:8ae67e9fb6ff |
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1 <tool id="gd_average_fst" name="Overall FST" version="1.0.0"> | |
2 <description>: Estimate the relative fixation index between two populations</description> | |
3 | |
4 <command interpreter="python"> | |
5 average_fst.py "$input" "$p1_input" "$p2_input" "$data_source.ds_choice" "$data_source.min_value" "$discard_fixed" "$biased" "$output" | |
6 #if $use_randomization.ur_choice == '1' | |
7 "$use_randomization.shuffles" "$use_randomization.p0_input" | |
8 #else | |
9 "0" "/dev/null" | |
10 #end if | |
11 #for $individual, $individual_col in zip($input.dataset.metadata.individual_names, $input.dataset.metadata.individual_columns) | |
12 #set $arg = '%s:%s' % ($individual_col, $individual) | |
13 "$arg" | |
14 #end for | |
15 </command> | |
16 | |
17 <inputs> | |
18 <param name="input" type="data" format="gd_snp" label="SNP table" /> | |
19 <param name="p1_input" type="data" format="gd_indivs" label="Population 1 individuals" /> | |
20 <param name="p2_input" type="data" format="gd_indivs" label="Population 2 individuals" /> | |
21 | |
22 <conditional name="data_source"> | |
23 <param name="ds_choice" type="select" format="integer" label="Data source"> | |
24 <option value="0" selected="true">sequence coverage and ..</option> | |
25 <option value="1">estimated genotype and ..</option> | |
26 </param> | |
27 <when value="0"> | |
28 <param name="min_value" type="integer" min="1" value="1" label="Minimum total read count for a population" /> | |
29 </when> | |
30 <when value="1"> | |
31 <param name="min_value" type="integer" min="1" value="1" label="Minimum individual genotype quality" /> | |
32 </when> | |
33 </conditional> | |
34 | |
35 <param name="discard_fixed" type="select" label="Apparently fixed SNPs"> | |
36 <option value="0">Retain SNPs that appear fixed in the two populations</option> | |
37 <option value="1" selected="true">Delete SNPs that appear fixed in the two populations</option> | |
38 </param> | |
39 | |
40 <param name="biased" type="select" label="FST estimator"> | |
41 <option value="0" selected="true">Wright's original definition</option> | |
42 <option value="1">Weir's unbiased estimator</option> | |
43 </param> | |
44 | |
45 <conditional name="use_randomization"> | |
46 <param name="ur_choice" type="select" format="integer" label="Use randomization"> | |
47 <option value="0" selected="true">No</option> | |
48 <option value="1">Yes</option> | |
49 </param> | |
50 <when value="0" /> | |
51 <when value="1"> | |
52 <param name="shuffles" type="integer" min="0" value="0" label="Shuffles" /> | |
53 <param name="p0_input" type="data" format="gd_indivs" label="Individuals for randomization" /> | |
54 </when> | |
55 </conditional> | |
56 </inputs> | |
57 | |
58 <outputs> | |
59 <data name="output" format="txt" /> | |
60 </outputs> | |
61 | |
62 <tests> | |
63 <test> | |
64 <param name="input" value="test_in/sample.gd_snp" ftype="gd_snp" /> | |
65 <param name="p1_input" value="test_in/a.gd_indivs" ftype="gd_indivs" /> | |
66 <param name="p2_input" value="test_in/b.gd_indivs" ftype="gd_indivs" /> | |
67 <param name="ds_choice" value="0" /> | |
68 <param name="min_value" value="3" /> | |
69 <param name="discard_fixed" value="1" /> | |
70 <param name="biased" value="0" /> | |
71 <param name="ur_choice" value="0" /> | |
72 <output name="output" file="test_out/average_fst/average_fst.txt" /> | |
73 </test> | |
74 </tests> | |
75 | |
76 <help> | |
77 | |
78 **What it does** | |
79 | |
80 The user specifies a SNP table and two "populations" of individuals, | |
81 both previously defined using the Specify Individuals tool. | |
82 No individual can be in both populations. Other choices are as follows. | |
83 | |
84 Data source. The allele frequencies of a SNP in the two populations can be | |
85 estimated either by the total number of reads of each allele, or by adding | |
86 the frequencies inferred from genotypes of individuals in the populations. | |
87 | |
88 After specifying the data source, the user sets lower bounds on amount | |
89 of data required at a SNP. For estimating the Fst using read counts, | |
90 the bound is the minimum count of reads of the two alleles in a population. | |
91 For estimations based on genotype, the bound is the minimum reported genotype | |
92 quality per individual. SNPs not meeting these lower bounds are ignored. | |
93 | |
94 The user specifies whether SNPs where both populations appear to be fixed | |
95 for the same allele should be retained or discarded. | |
96 | |
97 The user chooses which definition of Fst to use: Wright's original definition | |
98 or Weir's unbiased estimator. | |
99 | |
100 Finally, the user decides whether to use randomizations. If so, then the | |
101 user specifies how many randomly generated population pairs (retaining | |
102 the numbers of individuals of the originals) to generate, as well as the | |
103 "population" of additional individuals (not in the first two populations) | |
104 that can be used in the randomization process. | |
105 | |
106 The program prints the average Fst for the original populations and the | |
107 number of SNPs used to compute it. If randomizations were requested, | |
108 it prints the average Fst for each randomly generated population pair, | |
109 ending with a summary that includes the maximum and average value, and the | |
110 highest-scoring population pair. | |
111 | |
112 </help> | |
113 </tool> |