Mercurial > repos > miller-lab > genome_diversity
diff aggregate_gd_indivs.xml @ 13:fdb4240fb565
Uploaded Miller Lab Devshed version a51c894f5bed
author | miller-lab |
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date | Fri, 28 Sep 2012 11:34:31 -0400 |
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children | f04f40a36cc8 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/aggregate_gd_indivs.xml Fri Sep 28 11:34:31 2012 -0400 @@ -0,0 +1,86 @@ +<tool id="gd_sum_gd_snp" name="Aggregate Individuals" version="1.0.0"> + <description>: Append summary columns for a population</description> + + <command interpreter="python"> + modify_snp_table.py "$input" "$p1_input" "$output" "-1" "-1" "-1" "-1" + #for $individual, $individual_col in zip($input.dataset.metadata.individual_names, $input.dataset.metadata.individual_columns) + #set $arg = '%s:%s' % ($individual_col, $individual) + "$arg" + #end for + </command> + + <inputs> + <param name="input" type="data" format="gd_snp" label="SNP dataset" /> + <param name="p1_input" type="data" format="gd_indivs" label="Population individuals" /> + </inputs> + + <outputs> + <data name="output" format="gd_snp" metadata_source="input" /> + </outputs> + + <tests> + <test> + <param name="input" value="test_in/sample.gd_snp" ftype="gd_snp" /> + <param name="p1_input" value="test_in/a.gd_indivs" ftype="gd_indivs" /> + <param name="choice" value="1" /> + <param name="lo_coverage" value="0" /> + <param name="hi_coverage" value="1000" /> + <param name="low_ind_cov" value="3" /> + <param name="lo_quality" value="30" /> + <output name="output" file="test_out/modify_snp_table/modify.gd_snp" /> + </test> + </tests> + + <help> + +**Dataset formats** + +The input datasets are in gd_snp_ and gd_indivs_ formats. +The output dataset is in gd_snp_ format. (`Dataset missing?`_) + +.. _gd_snp: ./static/formatHelp.html#gd_snp +.. _gd_indivs: ./static/formatHelp.html#gd_indivs +.. _Dataset missing?: ./static/formatHelp.html + +----- + +**What it does** + +The user specifies that some of the individuals in a gd_snp dataset form a +"population", by supplying a list that has been previously created using the +Specify Individuals tool. The program appends a +new "entity" (set of four columns) to the gd_snp table, analogous to the columns +for an individual but containing summary data for the population as a group. +These four columns give the total counts for the two alleles, the "genotype" for +the population, and the maximum quality value, taken over all individuals in the +population. If all defined genotypes in the population are 2 (agree with the +reference), then the population's genotype is 2, and similarly for 0; otherwise +the genotype is 1 (unless all individuals have undefined genotype, in which case +it is -1). + +----- + +**Example** + +- input gd_snp:: + + Contig161_chr1_4641264_4641879 115 C T 73.5 chr1 4641382 C 6 0 2 45 8 0 2 51 15 0 2 72 5 0 2 42 6 0 2 45 10 0 2 57 Y 54 0.323 0 + Contig48_chr1_10150253_10151311 11 A G 94.3 chr1 10150264 A 1 0 2 30 1 0 2 30 1 0 2 30 3 0 2 36 1 0 2 30 1 0 2 30 Y 22 +99. 0 + Contig20_chr1_21313469_21313570 66 C T 54.0 chr1 21313534 C 4 0 2 39 4 0 2 39 5 0 2 42 4 0 2 39 4 0 2 39 5 0 2 42 N 1 +99. 0 + etc. + +- input individuals:: + + 9 PB1 + 13 PB2 + 17 PB3 + +- output:: + + Contig161_chr1_4641264_4641879 115 C T 73.5 chr1 4641382 C 6 0 2 45 8 0 2 51 15 0 2 72 5 0 2 42 6 0 2 45 10 0 2 57 Y 54 0.323 0 29 0 2 72 + Contig48_chr1_10150253_10151311 11 A G 94.3 chr1 10150264 A 1 0 2 30 1 0 2 30 1 0 2 30 3 0 2 36 1 0 2 30 1 0 2 30 Y 22 +99. 0 3 0 2 30 + Contig20_chr1_21313469_21313570 66 C T 54.0 chr1 21313534 C 4 0 2 39 4 0 2 39 5 0 2 42 4 0 2 39 4 0 2 39 5 0 2 42 N 1 +99. 0 13 0 2 42 + etc. + + </help> +</tool>