Mercurial > repos > miller-lab > genome_diversity
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author | miller-lab |
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date | Mon, 06 Jul 2015 10:32:24 -0400 |
parents | a631c2f6d913 |
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<tool id="gd_calc_freq" name="Rank Pathways" version="1.2.0"> <description>: Assess the impact of a gene set on KEGG pathways</description> <command interpreter="python"> #if $rank_by.choice == 'pct' rank_pathways_pct.py --input '$rank_by.input1' --columnENSEMBLT '$rank_by.t_col1' --inBckgrndfile '$rank_by.input2' --columnENSEMBLTBckgrnd '$rank_by.t_col2' --columnKEGGBckgrnd '$rank_by.k_col2' --statsTest '$rank_by.stat' --output '$output' #else if $rank_by.choice == 'paths' calclenchange.py '--loc_file=${GALAXY_DATA_INDEX_DIR}/gd.rank.loc' '--species=${rank_by.input.metadata.dbkey}' '--input=${rank_by.input}' '--output=${output}' '--posKEGGclmn=${rank_by.kpath}' '--KEGGgeneposcolmn=${rank_by.kgene}' #end if </command> <inputs> <conditional name="rank_by"> <param name="choice" type="select" label="Rank by"> <option value="pct" selected="true">percentage of genes affected</option> <option value="paths">change in length and number of paths</option> </param> <when value="pct"> <!-- using fields similar to the Rank Terms tool --> <param name="input1" type="data" format="tabular" label="Query dataset" /> <param name="t_col1" type="data_column" data_ref="input1" label="Column with ENSEMBL transcript codes" /> <param name="input2" type="data" format="tabular" label="Background dataset" /> <param name="t_col2" type="data_column" data_ref="input2" label="Column with ENSEMBL transcript codes" /> <param name="k_col2" type="data_column" data_ref="input2" label="Column with KEGG pathways" /> <param name="stat" type="select" label="Statistic for determining enrichment/depletion"> <option value="fisher" selected="true">two-tailed Fisher's exact test</option> <option value="hypergeometric">hypergeometric test</option> <option value="binomial">binomial probability</option> </param> </when> <when value="paths"> <param name="input" type="data" format="tabular" label="Dataset" /> <param name="kgene" type="data_column" data_ref="input" label="Column with KEGG gene ID" /> <param name="kpath" type="data_column" data_ref="input" numerical="false" label="Column with KEGG pathways" /> </when> </conditional> </inputs> <outputs> <data name="output" format="tabular" /> </outputs> <requirements> <requirement type="package" version="0.2.5">mechanize</requirement> <requirement type="package" version="1.8.1">networkx</requirement> <requirement type="package" version="0.1.4">fisher</requirement> </requirements> <tests> <test> </test> </tests> <help> **Dataset formats** The query dataset has a column containing ENSEMBL transcript codes for the gene set of interest, while the background dataset has one column with ENSEMBL transcript codes and another with KEGG pathways, for some larger universe of genes. All of the input and output datasets are in tabular_ format. The input dataset (i.e. query) to rank by "percentage of genes affected" has a column containing ENSEMBL transcript codes for the gene set of interest, while the background dataset has one column with ENSEMBL transcript codes and another with KEGG pathways, for some larger universe of genes. The input dataset to rank by "change in length and number of paths" must have columns with KEGG gene ID and pathways. The output datasets are described below. (`Dataset missing?`_) .. _tabular: ./static/formatHelp.html#tab .. _Dataset missing?: ./static/formatHelp.html ----- **What it does** Given a query set of genes from a larger background dataset, this tool evaluates the over- or under-representation of KEGG pathways in the query set, using the specified statistical test. Alternatively, the tool ranks the pathways based on the change in length and number of paths connecting sources and sinks. This change is calculated between graphs representing pathways with and without excluding the nodes that represent the genes in an input list. Sources are all the nodes representing the initial reactants/products in the pathway. Sinks are all the nodes representing the final reactants/products in the pathway. If pathways are ranked by percentage of genes affected, the output contains a row for each KEGG pathway, with the following columns: 1. count: the number of genes in the query set that are in this pathway 2. representation: the percentage of this pathway's genes (from the background dataset) that appear in the query set 3. ranking of this pathway, based on its representation ("1" is highest) 4. probability of depletion of this pathway in the query dataset 5. probability of enrichment of this pathway in the query dataset 6. name of the pathway If pathways are ranked by change in length and number of paths, the output is a tabular dataset with the following columns: 1. change in the mean length of paths between sources and sinks 2. mean length of paths between sources and sinks in the pathway including the genes in the input dataset. If the pathway do not have sources/sinks, the length is assumed to be infinite (I) 3. mean length of paths between sources and sinks in the pathway excluding the genes in the input dataset. If the pathway do not have sources/sinks, the length is assumed to be infinite (I) 4. rank of the change in the mean length of paths between sources and sinks (from high change to low change) 5. change in the number of paths between sources and sinks 6. number of paths between sources and sinks in the pathway including the genes in the input dataset. If the pathway do not have sources/sinks, it is assumed to be a circuit (C) 7. number of paths between sources and sinks in the pathway excluding the genes in the input dataset. If the pathway do not have sources/sinks, it is assumed to be a circuit (C) 8. rank of the change in the number of paths between sources and sinks (from high change to low change) 9. name of the pathway ----- **Examples** Rank by percentage of genes affected: - input background dataset (column 5 for ENSEMBL transcript, column 12 for KEGG pathways, two-tailed Fisher's exact test for statistic):: Contig39_chr1_3261104_3261850 414 chr1 3261546 ENSCAFT00000000001 ENSCAFP00000000001 S 667 F 476153 probably damaging cfa00230=Purine metabolism.cfa00500=Starch and sucrose metabolism.cfa00740=Riboflavin metabolism.cfa00760=Nicotinate and nicotinamide metabolism.cfa00770=Pantothenate and CoA biosynthesis.cfa01100=Metabolic pathways Contig62_chr1_19011969_19012646 265 chr1 19012240 ENSCAFT00000000144 ENSCAFP00000000125 * 161 R 483960 probably damaging N etc. - input query dataset (column 5 for ENSEMBL transcript):: Contig12_chr20_101969_112646 265 chr20 9822141 ENSCAFT00000001234 ENSCAFP00000021123 T 101 R 476153 probably damaging Contig39_chr1_3261104_3261850 414 chr1 3261546 ENSCAFT00000000001 ENSCAFP00000000001 S 667 F 476153 probably damaging etc. - output:: 3 0.20 1 1.0 0.0065 cfa03450=Non-homologous end-joining 1 0.067 2 1.0 0.019 cfa00750=Vitamin B6 metabolism 2 0.062 3 1.0 0.021 cfa00290=Valine, leucine and isoleucine biosynthesis 1 0.037 4 1.0 0.035 cfa00770=Pantothenate and CoA biosynthesis etc. Rank by change in length and number of paths: - input (column 10 for KEGG gene ID, column 12 for KEGG pathways):: Contig39_chr1_3261104_3261850 414 chr1 3261546 ENSCAFT00000000001 ENSCAFP00000000001 S 667 F 476153 probably damaging cfa00230=Purine metabolism.cfa00500=Starch and sucrose metabolism.cfa00740=Riboflavin metabolism.cfa00760=Nicotinate and nicotinamide metabolism.cfa00770=Pantothenate and CoA biosynthesis.cfa01100=Metabolic pathways Contig62_chr1_19011969_19012646 265 chr1 19012240 ENSCAFT00000000144 ENSCAFP00000000125 * 161 R 483960 probably damaging N etc. - output:: 3.64 8.44 4.8 2 4 9 5 1 cfa00260=Glycine, serine and threonine metabolism 7.6 9.6 2 1 3 5 2 2 cfa00240=Pyrimidine metabolism 0.05 2.67 2.62 6 1 30 29 3 cfa00982=Drug metabolism - cytochrome P450 -0.08 8.33 8.41 84 1 30 29 3 cfa00564=Glycerophospholipid metabolism etc. </help> </tool>