# HG changeset patch # User ning # Date 1363386194 14400 # Node ID 1108020e2d84f347334d0c47b14043c6fcaca3b7 # Parent 696a1f7e23fdd8c74ac186109950ab6c1e92705b Uploaded diff -r 696a1f7e23fd -r 1108020e2d84 EBGeneMultiCondTest.xml --- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/EBGeneMultiCondTest.xml Fri Mar 15 18:23:14 2013 -0400 @@ -0,0 +1,34 @@ + + Runs EBSeq to find DE genes across multiple (more than two) conditions + R --quiet --slave --file=$GALAXY_ROOT_DIR/tools/EBSeq/EBGeneMultiCondTest.R --args $Gene_Expression $First_Row_Sample_Names $Conditions $Patterns $PP_of_each_pattern $Pattern_with_highest_PP $Sizes + + + + + + + + + + + + + + + + + +The input Conditions should have exactly two levels. The length of the Condition vector should be exactly the same as the number of columns in the data file (except the gene names column). + +The patterns of interests could be obtained by function Get All Possible Patterns (and optionally, if there are too many patterns generated, the function Choose Patterns could be used to choose only subset of the patterns.) + +Three output files will be generated. The first file contains the Posterior probability of being each pattern. The second file contains the pattern with highest PP for each gene and the normalized expressions. Genes are with the same order as in input file. +The last file provides the library size factor for each sample. + + + + + +