Description Usage Arguments See Also
Perform Bayesian NMF mutational signature analysis. Source code borrowed from Broad Institute CGA.
1 | BayesNMF.MutationalSignatures(x, tumor.type="tumor.type", hyper=FALSE, fafile=NULL, out.dir="OUTPUT_lego96", prior="L1KL")
|
x |
A data frame with at least 6 named columns, i.e. 'chr', 'start', 'end', 'ref', 'alt' and 'sampleid'. The seqlevels of mutation data and reference must be identical, or ERROR will occur during mutation context extraction. |
tumor.type |
A character string specify tumor type analyzed. |
hyper |
Default = FALSE ; TRUE - to reduce the effect of hyper-mutant samples in the signature discovery. |
fafile |
BWA-indexed reference sequence. If this is NULL (default), the Homo sapiens hg19 in package |
out.dir |
The output directory. |
prior |
Default = L1KL (expoential priors); L2KL (half-normal priors). |
Mutational signature analysis framework in package SomaticSignatures
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