voomWithQualityWeights(counts, design=NULL, lib.size=NULL, normalize.method="none", plot=FALSE, span=0.5, var.design=NULL, method="genebygene", maxiter=50, tol=1e-10, trace=FALSE, replace.weights=TRUE, col=NULL, ...)matrix containing raw counts, or an ExpressionSet containing raw counts, or a DGEList object.NULL and counts is a DGEList then, the normalized library sizes are taken from counts.
Otherwise library sizes are calculated from the columnwise counts totals.method argument of normalizeBetweenArrays when the data is single-channel.logical, should a plot of the mean-variance trend and sample-specific weights be displayed?NULL."genebygene" and "reml"."genebygene" algorithm.EList object from voom is returned.
If FALSE, then a matrix of combined weights is returned.plot=TRUE). If NULL, bars are plotted in grey.lmFit.counts containing consolidated voom and sample-specific weights.
If replace.weights=TRUE, then an EList object is returned with the weights component containing the consolidated weights.
It combines observational-level weights from voom with sample-specific weights estimated using the arrayWeights function.
Liu, R., Holik, A. Z., Su, S., Jansz, N., Chen, K., Leong, H. S., Blewitt, M. E., Asselin-Labat, M.-L., Smyth, G. K., Ritchie, M. E. (2015). Why weight? Combining voom with estimates of sample quality improves power in RNA-seq analyses. Nucleic Acids Research 43. (Accepted 17 April 2015)
Ritchie, M. E., Diyagama, D., Neilson, van Laar, R., J., Dobrovic, A., Holloway, A., and Smyth, G. K. (2006). Empirical array quality weights in the analysis of microarray data. BMC Bioinformatics 7, 261. http://www.biomedcentral.com/1471-2105/7/261
voom, arrayWeightsA summary of functions for RNA-seq analysis is given in 11.RNAseq.