nullp | R Documentation |
Calculates a Probability Weighting Function for a set of genes based on a given set of biased data (usually gene length) and each genes status as differentially expressed or not.
nullp(DEgenes, genome, id, bias.data=NULL,plot.fit=TRUE)
DEgenes |
A named binary vector where 1 represents DE, 0 not DE and the names are gene IDs. |
genome |
A string identifying the genome that |
id |
A string identifying the gene identifier used by |
bias.data |
A numeric vector containing the data on which the DE may depend. Usually this is the median transcript length of each gene in bp. If set to |
plot.fit |
Plot the PWF or not? Calls |
It is essential that the entire analysis pipeline, from summarizing raw reads through to using goseq
be done in just one gene identifier format. If your data is in a different format you will need to obtain the gene lengths and supply them to the nullp
function using the bias.data
arguement. Converting to a supported format from another format should be avoided whenever possible as this will almost always result in data loss.
NA
s are allowed in the bias.data vector if you do not have information about a certain gene. Setting a gene to NA
is preferable to removing it from the analysis.
If bias.data
is left as NULL
, nullp
attempts to use getlength
to fetch GO catgeory to gene identifier mappings.
It is recommended you review the fit produced by the nullp
function before proceeding by leaving plot.fit
as TRUE
.
A data frame with 3 columns, named "DEgenes", "bias.data" and "pwf" with the rownames set to the gene names. Each row corresponds to a gene with the DEgenes column specifying if the gene is DE (1 for DE, 0 for not DE), the bias.data column giving the numeric value of the DE bias being accounted for (usually the gene length or number of counts) and the pwf column giving the genes value on the probability weighting function. This object is usually passed to goseq
to calculate enriched categories or plotPWF
for further plotting.
Matthew D. Young myoung@wehi.edu.au
Young, M. D., Wakefield, M. J., Smyth, G. K., Oshlack, A. (2010) Gene ontology analysis for RNA-seq: accounting for selection bias Genome Biology Date: Feb 2010 Vol: 11 Issue: 2 Pages: R14
supportedGenomes
, supportedGeneIDs
, goseq
, getlength
data(genes) pwf <- nullp(genes, 'hg19', 'ensGene')
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