Mercurial > repos > melissacline > ucsc_cancer_browser_stats
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author | jingchunzhu |
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date | Fri, 31 Jul 2015 13:32:25 -0700 |
parents | a04e3c59e117 |
children | fd8529cd1564 |
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<tool id="ucscCancerBrowserStats" description="t-tests of Difference in genomic data" name="Difference between categories (t-test)" version="0.0.1"> <command interpreter="python"> stats.py $genomicMatrix $clinicalFeatures $outFile -a="${category1}" -b="${category2}" </command> <inputs> <param format="tabular" name="genomicMatrix" type="data" label="Genomic Matrix"/> <param format="tabular" name="clinicalFeatures" type="data" label="Phenotype Matrix"/> <param type="text" name="category1" label="Category 1" optional="false"/> <param type="text" name="category2" label="Category 2" optional="false"/> </inputs> <outputs> <data format="tabular" name="outFile" /> </outputs> <requirements> <requirement type="package" version="1.0" >cancerBrowserStats</requirement> </requirements> <tests> <param name="genomicMatrix" value="sample.genomic.matrix.txt" /> <param name="clinicalMatrix" value="sample.clinical.matrix.txt" /> <param name="category1" value="A"/> <param name="category2" value="B"/> <output name="outFile" value="sample.stats.output.txt"/> </tests> <help> This tool performs statistical tests found in the UCSC Cancer Genomics Browser. The input data is a genomic matrix (containing genomic data, with rows representing genes or probes and columns representing samples or patients), a clinical matrix of two (or more) columns assigning categorical values to the samples, and two categorical values of interest. The tool identifies the samples corresponding to each categorical value, then identifies the columns in the genomic matrix corresponding to those sets of samples, which identifies two groups of columns. For each row in the genomic matrix, it extracts the value for those two sets of columns, performs a t-test on the two sets of values, and returns the result for the row. Any values for any columns NOT pertaining to one of the categorical values of interest are ignored. The user runs this tool with th following steps: 1. Specify a genomic matrix. The expected format is with rows representing genes and columns representing samples, and the first line contains sample names. 2. Specify a clinical matrix. Here, rows indicate samples, columns indicate clinical features, and the header row contains feature names. The first column MUST indicate the sample names, and MUST correspond to the column names of the genomic matrix. The clinical feature of interest MUST be in the second column. Any other columns will be ignored. 3. Indicate two clinical values that you want to use for defining the two groups. For example, the two groups could be "Red group" and "Green group", 0 and 1, or whatever. The output indicates, for each row, the t-statistic reporting on the difference between the two groups of columns (as specified by the two clinical values), the p-value corresponding to that t-statistic, the median value for each group, and the difference between the medians. If it cannot calculate these values, it returns a vector of NAs. For example, given the following genomic matrix for (1):: Gene 1 2 3 4 5 6 7 8 9 10 G1 2.0 2.2 3.2 1.1 5.1 8.1 3.2 1.1 8.1 0.2 G2 0.1 8.2 9.1 4.2 6.1 4.9 3.9 2.3 1.1 0.2 and given the following clinical matrix for (2):: sample_id Value 1 A 2 A 3 B 4 C 5 B 6 B 7 A 8 A 9 B 10 A and given A for Category 1 and B for Category 2 the tool will assemble the following two groups of values:: G1 A:(2.0, 2.2, 3.2, 1.1, 0.2) B:(3.2, 5.1, 8.1, 8.1) G2 A:(0.1, 8.2, 3.9, 2.3, 0.2) B:(9.1, 6.1, 4.9, 1.1) Note that the values for sample_id 4 do not appear, because it has a Value of C in the second column, which is neither A nor B. And it will return the output:: Gene Statistic pValue Median1 Median2 Delta G1 -4.168999 0.004194 2.000000 6.600000 -4.600000 G2 -1.198486 0.269724 2.300000 5.500000 -3.200000 </help> </tool>