Mercurial > repos > miller-lab > genome_diversity
diff coverage_distributions.xml @ 12:4b6590dd7250
Uploaded
author | miller-lab |
---|---|
date | Wed, 12 Sep 2012 17:10:26 -0400 |
parents | |
children |
line wrap: on
line diff
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/coverage_distributions.xml Wed Sep 12 17:10:26 2012 -0400 @@ -0,0 +1,75 @@ +<tool id="gd_coverage_distributions" name="Coverage" version="1.0.0"> + <description>distributions</description> + + <command interpreter="python"> + coverage_distributions.py "$input" "0" "$output" "$output.files_path" + #if $individuals.choice == '0' + "all_individuals" + #else if $individuals.choice == '1' + #set $arg = 'individuals:%s' % str($individuals.p1_input) + "$arg" + #else if $individuals.choice == '2' + #for $population in $individuals.populations + #set $arg = 'population:%s:%s' % (str($population.p_input), str($population.p_input.name)) + "$arg" + #end for + #end if + #for $individual, $individual_col in zip($input.dataset.metadata.individual_names, $input.dataset.metadata.individual_columns) + #set $individual_arg = 'individual:%s:%s' % ($individual_col, $individual) + "$individual_arg" + #end for + </command> + + <inputs> + <param name="input" type="data" format="gd_snp" label="SNP table" /> + + <conditional name="individuals"> + <param name="choice" type="select" label="Individuals"> + <option value="0" selected="true">All</option> + <option value="1">Individuals in a population</option> + <option value="2">Population totals</option> + </param> + <when value="0" /> + <when value="1"> + <param name="p1_input" type="data" format="gd_indivs" label="Population individuals" /> + </when> + <when value="2"> + <repeat name="populations" title="Population" min="1"> + <param name="p_input" type="data" format="gd_indivs" label="individuals" /> + </repeat> + </when> + </conditional> + + <!-- + <param name="data_source" type="select" label="Data source"> + <option value="0" selected="true">Sequence coverage</option> + <option value="1">Genotype quality</option> + </param> + --> + </inputs> + + <outputs> + <data name="output" format="html" /> + </outputs> + + <tests> + <test> + <param name="input" value="test_in/sample.gd_snp" ftype="gd_snp" /> + <param name="choice" value="0" /> + <output name="output" file="test_out/coverage_distributions/coverage.html" ftype="html" compare="diff" lines_diff="2"> + <extra_files type="file" name="coverage.pdf" value="test_out/coverage_distributions/coverage.pdf" compare="sim_size" delta = "1000"/> + <extra_files type="file" name="coverage.txt" value="test_out/coverage_distributions/coverage.txt" /> + </output> + </test> + </tests> + + <help> +**What it does** + +This tool reports distributions of SNP reliability indicators for +individuals or populations. The reliability is measured by the sequence +coverage. Textual and graphical reports are generated, where the text +output gives the cumulative distributions. + </help> +</tool> +