Mercurial > repos > miller-lab > genome_diversity
annotate offspring_heterozygosity.xml @ 31:a631c2f6d913
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author | Richard Burhans <burhans@bx.psu.edu> |
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date | Fri, 20 Sep 2013 13:25:27 -0400 |
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1 <tool id="gd_offspring_heterozygosity" name="Pairs sequenced" version="1.0.0"> |
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2 <description>: Offspring estimated heterozygosity of sequenced pairs</description> |
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3 |
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4 <command interpreter="python"> |
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5 #import json |
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6 #import base64 |
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7 #import zlib |
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8 #set $ind_names = $input.dataset.metadata.individual_names |
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9 #set $ind_colms = $input.dataset.metadata.individual_columns |
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10 #set $ind_dict = dict(zip($ind_names, $ind_colms)) |
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11 #set $ind_json = json.dumps($ind_dict, separators=(',',':')) |
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12 #set $ind_comp = zlib.compress($ind_json, 9) |
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13 #set $ind_arg = base64.b64encode($ind_comp) |
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14 offspring_heterozygosity.py '$input' '$input.ext' '$ind_arg' '$p1_input' '$p2_input' '$output' |
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15 </command> |
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16 |
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17 <inputs> |
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18 <param name="input" type="data" format="gd_snp,gd_genotype" label="SNP dataset" /> |
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19 <param name="p1_input" type="data" format="gd_indivs" label="First individuals dataset" /> |
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20 <param name="p2_input" type="data" format="gd_indivs" label="Second individuals dataset" /> |
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21 </inputs> |
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22 |
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23 <outputs> |
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24 <data name="output" format="txt" /> |
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25 </outputs> |
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26 |
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27 <requirements> |
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28 <requirement type="package" version="0.1">gd_c_tools</requirement> |
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29 </requirements> |
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30 |
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31 <!-- |
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32 <tests> |
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33 </tests> |
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34 --> |
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35 |
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36 <help> |
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37 |
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38 **Dataset formats** |
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39 |
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40 The input datasets are in gd_snp_, gd_genotype_, and gd_indivs_ formats. |
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41 The output dataset is in text_ format. |
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42 |
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43 .. _gd_snp: ./static/formatHelp.html#gd_snp |
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44 .. _gd_genotype: ./static/formatHelp.html#gd_genotype |
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45 .. _gd_indivs: ./static/formatHelp.html#gd_indivs |
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46 .. _text: ./static/formatHelp.html#text |
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47 |
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48 ----- |
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49 |
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50 **What it does** |
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51 |
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52 For each pair of individuals, one from each specified set, the program |
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53 computes the expected heterozygosity of any offspring of the pair, i.e., |
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54 the probability that the offspring has distinct nucleotides at a randomly |
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55 chosen autosomal SNP. In other words, we add the following numbers for |
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56 each autosomal SNP where both genotypes are defined, then divide by the |
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57 number of those SNPs: |
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58 |
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59 0 if the individuals are homozygous for the same nucleotide |
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61 1 if the individuals are homozygous for different nucleotides |
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62 |
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63 1/2 otherwise (i.e., if one or both individuals are heterozygous) |
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64 |
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65 A SNP is ignored if one or both individuals have an undefined genotype |
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66 (designated as -1). |
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67 </help> |
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68 </tool> |