Inigo Martincorena and Moritz Gerstung

6 March 2015

ShearwaterML is a maximum-likelihood adaptation of the original Shearwater algorithm. Unlike the original algorithm, ShearwaterML does not use prior information and yields p-values, instead of Bayes factors, using a Likelihood-Ratio Test. This allows using standard multiple testing correction methods to obtain a list of significant variants with a controlled false discovery rate.

For a detailed description of the algorithm see:

Martincorena I, Roshan A, Gerstung M, et al. (2015). High burden and pervasive positive selection of somatic mutations in normal human skin. Science (2015).

Load data from deepSNV example

library(deepSNV)

## Loading required package: parallel

## Loading required package: IRanges

## Loading required package: BiocGenerics

## 
## Attaching package: 'BiocGenerics'

## The following objects are masked from 'package:stats':
## 
##     IQR, mad, sd, var, xtabs

## The following objects are masked from 'package:base':
## 
##     Filter, Find, Map, Position, Reduce, anyDuplicated, aperm, append,
##     as.data.frame, basename, cbind, colnames, dirname, do.call,
##     duplicated, eval, evalq, get, grep, grepl, intersect, is.unsorted,
##     lapply, mapply, match, mget, order, paste, pmax, pmax.int, pmin,
##     pmin.int, rank, rbind, rownames, sapply, saveRDS, setdiff, table,
##     tapply, union, unique, unsplit, which.max, which.min

## Loading required package: S4Vectors

## Loading required package: stats4

## 
## Attaching package: 'S4Vectors'

## The following object is masked from 'package:utils':
## 
##     findMatches

## The following objects are masked from 'package:base':
## 
##     I, expand.grid, unname

## Loading required package: GenomicRanges

## Loading required package: GenomeInfoDb

## Loading required package: SummarizedExperiment

## Loading required package: MatrixGenerics

## Loading required package: matrixStats

## 
## Attaching package: 'MatrixGenerics'

## The following objects are masked from 'package:matrixStats':
## 
##     colAlls, colAnyNAs, colAnys, colAvgsPerRowSet, colCollapse,
##     colCounts, colCummaxs, colCummins, colCumprods, colCumsums,
##     colDiffs, colIQRDiffs, colIQRs, colLogSumExps, colMadDiffs,
##     colMads, colMaxs, colMeans2, colMedians, colMins, colOrderStats,
##     colProds, colQuantiles, colRanges, colRanks, colSdDiffs, colSds,
##     colSums2, colTabulates, colVarDiffs, colVars, colWeightedMads,
##     colWeightedMeans, colWeightedMedians, colWeightedSds,
##     colWeightedVars, rowAlls, rowAnyNAs, rowAnys, rowAvgsPerColSet,
##     rowCollapse, rowCounts, rowCummaxs, rowCummins, rowCumprods,
##     rowCumsums, rowDiffs, rowIQRDiffs, rowIQRs, rowLogSumExps,
##     rowMadDiffs, rowMads, rowMaxs, rowMeans2, rowMedians, rowMins,
##     rowOrderStats, rowProds, rowQuantiles, rowRanges, rowRanks,
##     rowSdDiffs, rowSds, rowSums2, rowTabulates, rowVarDiffs, rowVars,
##     rowWeightedMads, rowWeightedMeans, rowWeightedMedians,
##     rowWeightedSds, rowWeightedVars

## Loading required package: Biobase

## Welcome to Bioconductor
## 
##     Vignettes contain introductory material; view with
##     'browseVignettes()'. To cite Bioconductor, see
##     'citation("Biobase")', and for packages 'citation("pkgname")'.

## 
## Attaching package: 'Biobase'

## The following object is masked from 'package:MatrixGenerics':
## 
##     rowMedians

## The following objects are masked from 'package:matrixStats':
## 
##     anyMissing, rowMedians

## Loading required package: Biostrings

## Loading required package: XVector

## 
## Attaching package: 'Biostrings'

## The following object is masked from 'package:base':
## 
##     strsplit

## Loading required package: VGAM

## Loading required package: splines

## Loading required package: VariantAnnotation

## Loading required package: Rsamtools

## 
## Attaching package: 'VariantAnnotation'

## The following object is masked from 'package:base':
## 
##     tabulate

## 
## Attaching package: 'deepSNV'

## The following objects are masked from 'package:VGAM':
## 
##     dbetabinom, pbetabinom

## The following object is masked from 'package:BiocGenerics':
## 
##     normalize

regions <- GRanges("B.FR.83.HXB2_LAI_IIIB_BRU_K034", IRanges(start = 3120, end=3140))
files <- c(system.file("extdata", "test.bam", package="deepSNV"), system.file("extdata", "control.bam", package="deepSNV"))
counts <- loadAllData(files, regions, q=30)

ShearwaterML: “betabinLRT” calculates p-values for each possible mutation

pvals <- betabinLRT(counts, rho=1e-4, maxtruncate = 1)$pvals
qvals <- p.adjust(pvals, method="BH")
dim(qvals) = dim(pvals)
vcfML = qvals2Vcf(qvals, counts, regions, samples = files, mvcf = TRUE)

Original Shearwater: “bbb” computes the original Bayes factors

bf <- bbb(counts, model = "OR", rho=1e-4)
vcfBF <- bf2Vcf(bf, counts, regions, samples = files, prior = 0.5, mvcf = TRUE)

plot(pvals[1,,], bf[1,,]/(1+bf[1,,]), log="xy")