Talk:RP.R

RP package:RankProd R Documentation Rank Product Analysis of Microarray Description: Perform rank product method to identify differentially expressed genes. It is possible to do either a one-class or two-class analysis. Usage: RP(data,cl,num.perm=100,logged=TRUE, na.rm=FALSE,gene.names=NULL,plot=FALSE, rand=NULL) Arguments: data: the data set that should be analyzed. Every row of this data set must correspond to a gene. cl: a vector containing the class labels of the samples. In the two class unpaired case, the label of a sample is either 0 (e.g., control group) or 1 (e.g., case group). For one class data, the label for each sample should be 1. num.perm: number of permutations used in the calculation of the null density. Default is 'num.perm=100'. logged: if "TRUE", data has bee logged, otherwise set it to "FALSE" na.rm: if 'FALSE' (default), the NA value will not be used in computing rank. If 'TRUE', the missing values will be replaced by the gene-wise mean of the non-missing values. Gene with all values missing will be assigned "NA" gene.names: if "NULL", no gene name will be assigned to the estimated percentage of false positive predictions (pfp). plot: If "TRUE", plot the estimated pfp verse the rank of each gene. rand: if specified, the random number generator will be put in a reproducible state using the rand value as seed. Value: A result of identifying differentially expressed genes between two classes. The identification consists of two parts, the identification of up-regulated and down-regulated genes in class 2 compared to class 1, respectively. pfp: estimated percentage of false positive predictions (pfp) up to the position of each gene under two identificaiton each pval: estimated pvalue for each gene being up- and down-regulated RPs: Original rank-product of each genes for two dentificaiton each RPrank: rank of the rank product of each genes Orirank: original rank in each comparison, which is used to construct rank product AveFC: fold change of average expression under class 1 over that under class 2. log-fold change if data is in log scaled, original fold change if data is unlogged. Note: Percentage of false prediction (pfp), in theory, is equivalent of false discovery rate (FDR), and it is possible to be large than 1. The function looks for up- and down- regulated genes in two seperate steps, thus two pfps and pvalues are computed and used to identify gene that belong to each group. This function is suitable to deal with data from a single origin, e.g. single experiment. If the data has different origin, e.g. generated at different laboratories, please refer RP.advance. Author(s): Fangxin Hong fhong@salk.edu References: Breitling, R., Armengaud, P., Amtmann, A., and Herzyk, P.(2004) Rank Products:A simple, yet powerful, new method to detect differentially regulated genes in replicated microarray experiments, _FEBS Letter_, 57383-92 See Also: 'topGene' 'RPadvance' 'plotRP' Examples: # Load the data of Golub et al. (1999). data(golub) # contains a 3051x38 gene expression # matrix called golub, a vector of length called golub.cl # that consists of the 38 class labels, # and a matrix called golub.gnames whose third column # contains the gene names. data(golub) #use a subset of data as example, apply the rank #product method subset <- c(1:4,28:30) #Setting rand=123, to make the results reproducible, RP.out <- RP(golub[,subset],golub.cl[subset],rand=123) # class 2: label =1, class 1: label = 0 #pfp for identifying genes that are up-regulated in class 2 #pfp for identifying genes that are down-regulated in class 2 head(RP.out$pfp)

RankProd1

The following line is suspect as it always pads out data.rep NA's with 1 in rank.rep

 rank.rep[is.na(data.rep)] = 1