Mercurial > repos > miller-lab > genome_diversity
diff dpmix.xml @ 0:2c498d40ecde
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author | miller-lab |
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date | Mon, 09 Apr 2012 12:03:06 -0400 |
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children | 7a94f11fe71f |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/dpmix.xml Mon Apr 09 12:03:06 2012 -0400 @@ -0,0 +1,68 @@ +<tool id="gd_dpmix" name="Admixture" version="1.0.0"> + <description>using dynamic programming</description> + + <command interpreter="python"> + dpmix.py "$input" "$data_source" "$switch_penalty" "$ap1_input" "$ap2_input" "$p_input" "$output" "$output2" "$output2.extra_files_path" "$input.dataset.metadata.dbkey" "$input.dataset.metadata.ref" "$GALAXY_DATA_INDEX_DIR" "gd.heterochromatic.loc" + #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="wsf" label="Dataset"> + <validator type="unspecified_build" message="This dataset does not have a reference species and cannot be used with this tool" /> + </param> + <param name="ap1_input" type="data" format="ind" label="Ancestral population 1 individuals" /> + <param name="ap2_input" type="data" format="ind" label="Ancestral population 2 individuals" /> + <param name="p_input" type="data" format="ind" label="Potentially admixed individuals" /> + + <param name="data_source" type="select" format="integer" label="Data source"> + <option value="0" selected="true">sequence coverage</option> + <option value="1">estimated genotype</option> + </param> + + <param name="switch_penalty" type="integer" min="0" value="10" label="Switch penalty" /> + </inputs> + + <outputs> + <data name="output" format="tabular" /> + <data name="output2" format="html" /> + </outputs> + + <tests> + <test> + <param name="input" value="test_in/sample.wsf" ftype="wsf" /> + <param name="ap1_input" value="test_in/a.ind" ftype="ind" /> + <param name="ap2_input" value="test_in/b.ind" ftype="ind" /> + <param name="p_input" value="test_in/c.ind" ftype="ind" /> + <param name="data_source" value="0" /> + <param name="switch_penalty" value="10" /> + + <output name="output" file="test_out/dpmix/dpmix.tabular" /> + + <output name="output2" file="test_out/dpmix/dpmix.html" ftype="html" compare="diff" lines_diff="2"> + <extra_files type="file" name="dpmix.pdf" value="test_out/dpmix/dpmix.pdf" compare="sim_size" delta = "10000" /> + <extra_files type="file" name="misc.txt" value="test_out/dpmix/misc.txt" /> + </output> + </test> + </tests> + + <help> +**What it does** + +The user specifies two "ancestral" populations (i.e., sources for +chromosomes) and a set of potentially admixed individuals, and chooses +between the sequence coverage or the estimated genotypes to measure +the similarity of genomic intervals in admixed individuals to the two +classes of ancestral chromosomes. The user also picks a "switch penalty", +typically between 10 and 100. For each potentially admixed individual, +the program divides the genome into three "genotypes": (0) homozygous +for the second ancestral population (i.e., both chromosomes from that +population), (1) heterozygous, or (2) homozygous for the second ancestral +population. Parts of a chromosome that are labeled as "heterochromatic" +are given the non-genotype, 3. Smaller values of the switch penalty +(corresponding to more ancient admixture events) generally lead to the +reconstruction of more frequent changes between genotypes. + </help> +</tool>