Paths(signatures$SignExposures)
Motivation: Cancer is an evolutionary process driven by continuous acquisition of genetic variations in individual cells. The diversity and complexity of somatic mutational processes is a conspicuous feature orchestrated by DNA damage agents and repair processes, including exogenous or endogenous mutagen exposures, defects in DNA mismatch repair and enzymatic modification of DNA. The identification of the underlying mutational processes is central to understanding of cancer origin and evolution.
The signeR package focuses on the estimation and further analysis of mutational signatures. The functionalities of this package can be divided into three categories. First, it provides tools to process VCF files and generate matrices of SNV mutation counts and mutational opportunities, both defined according to a 3bp context (mutation site and its neighbouring 3' and 5' bases). Second, these count matrices are considered as input for the estimation of the underlying mutational signatures and the number of active mutational processes. Third, the package provides tools to correlate the activities of those signatures with other relevant information such as clinical data, in order to draw conclusions about the analysed genome samples, which can be useful for clinical applications. These include the Differential Exposure Score and the a posteriori sample classification.
Although signeR is intended for the estimation of mutational signatures, it actually provides a full Bayesian treatment to the non-negative matrix factorisation (NMF) model. Further details about the method can be found in Rosales & Drummond et al., 2016 (see section 9.1 below).
This vignette briefly explains the use of signeR through examples.
Before installing, please make sure you have the latest version of R and Bioconductor installed.
To install signeR, start R and enter:
install.packages("BiocManager") BiocManager::install("signeR")
For more information, see this page.
Once installed the library can be loaded as
library(signeR)
signeR takes as input a count matrix of samples x features. Each feature is usually a SNV mutation within a 3bp context (96 features, 6 types of SNV mutations and 4 possibilities for the bases at each side of the SNV change). Optionally, an opportunity matrix can also be provided containing the count frequency of the features in the whole analyzed region for each sample. Although not required, this argument is highly recommended because it allows signeR to normalize the features frequency over the analyzed region.
Input matrices can be read both from a VCF or a tab-delimited files, as described next.
The VCF file format is the most common format for storing genetic variations, the signeR package includes a utility function for generating a count matrix from the VCF:
library(VariantAnnotation) # BSgenome, equivalent to the one used on the variant call library(BSgenome.Hsapiens.UCSC.hg19) vcfobj <- readVcf("/path/to/a/file.vcf", "hg19") mut <- genCountMatrixFromVcf(BSgenome.Hsapiens.UCSC.hg19, vcfobj)
This function will generate a matrix of mutation counts for each sample in the provided VCF.
If you have one vcf per sample you can combine the results into a single matrix like this:
mut = matrix(ncol=96,nrow=0) for(i in vcf_files) { vo = readVcf(i, "hg19") # sample name (should pick up from the vcf automatically if available) # colnames(vo) = i m0 = genCountMatrixFromVcf(mygenome, vo) mut = rbind(mut, m0) } dim(mut) # matrix with all samples
The opportunity matrix can also be generated from the reference genome (hg19 in the following case):
library(rtracklayer) target_regions <- import(con="/path/to/a/target.bed", format="bed") opp <- genOpportunityFromGenome(BSgenome.Hsapiens.UCSC.hg19, target_regions, nsamples=nrow(mut))
Where target.bed is a bed file
containing the genomic regions analyzed by the variant caller.
If a BSgenome is not available for your genome, you can use a fasta file:
library(Rsamtools) # make sure /path/to/genome.fasta.fai exists ! # you can use "samtools faidx" command to create it mygenome <- FaFile("/path/to/genome.fasta") mut <- genCountMatrixFromVcf(mygenome, vcfobj) opp <- genOpportunityFromGenome(mygenome, target_regions)
By convention, the input file should be tab-delimited with sample names as row names and features as column names. Features should be refered in the format "base change:triplet", e.g. "C>A:TCG", as can be seen in the example below. Similarly, the opportunity matrix can be provided in a tab-delimited file with the same structure as the mutation counts file. An example of the required matrix format can be seen here.
This tutorial uses as input the 21 breast cancer dataset described in
Nik-Zainal et al 2012. For the sake of convenience this dataset is
included with the package and can be accessed by using the
system.file function:
mut <- read.table(system.file("extdata","21_breast_cancers.mutations.txt", package="signeR"), header=TRUE, check.names=FALSE) opp <- read.table(system.file("extdata","21_breast_cancers.opportunity.txt", package="signeR"))
signeR analysis can incorporate any previous knowledge about the signatures present in the dataset. If signatures are known in advance, they can be provided as a matrix, which may be used by signeR in two different ways: a starting value that will be updated according to mutation patterns found on present data or a fixed set of parameters, kept unchanged during the estimation of exposures.
Signatures matrix shall contain each signature in one colum. An example of the required matrix format can be seen here.
Along this tutorial a matrix of signatures found in breast cancer, as described in
Cosmic database. For the sake of convenience this matrix is included with the
package and can be accessed by the
system.file function:
Pmatrix <- as.matrix(read.table(system.file("extdata","Cosmic_signatures_BRC.txt", package="signeR"), sep="\t", check.names=FALSE))
signeR takes a count matrix as its only required parameter, but the user can provide an opportunity matrix as well. The algorithm allows the assessment of the number of signatures by three options, as follows.
signatures <- signeR(M=mut, Opport=opp)
signatures <- signeR(M=mut, Opport=opp, nlim=c(3,7))
signatures <- signeR(M=mut, Opport=opp, nsig=3, main_eval=100, EM_eval=50, EMit_lim=20)
signatures.Pstart <- signeR(M=mut, Opport=opp, P=Pmatrix, fixedP=FALSE, main_eval=100, EM_eval=50, EMit_lim=20)
The parameters testing_burn and testing_eval
control the number of iterations used to estimate the number of signatures
(default value is 1000 for both parameters). There are other
arguments that may be passed on to signeR. Please have a look at signeR's
manual, issued by typing help(signeR).
Whenever signeR is left to decide which number of signatures is optimal, it will search for the rank Nsig that maximizes the median Bayesian Information Criterion (BIC). After the processing is done, this information can be plotted by the following command:
BICboxplot(signatures)
Boxplot of BIC values, showing that the optimal number of signatures for this dataset is 5.
signeR also offer the possibility to estimate exposures to known signatures as, for example, the ones described on Cosmic database. In this case, signatures should be provided in a matrix, as described in intem 3.3 above, and should be kept constant during analysis:
Pmatrix <- as.matrix(read.table(system.file("extdata","Cosmic_signatures_BRC.txt", package="signeR"), sep="\t", check.names=FALSE))
The following command will make signeR estimate the exposures to the Cosmic signatures found on breast cancer:
exposures.known.sigs <- signeR(M=mut, Opport=opp, P=Pmatrix, fixedP=TRUE, main_eval=100, EM_eval=50, EMit_lim=20)
Exposures can then be recovered from the signer output by the following command (as in any signer analysis):
exposures <- Median_exp(exposures.known.sigs$SignExposures)
signeR offer several plots to visualize estimated signatures and their exposures, as weel as the convergence of the MCMC used to estimate them.
The following instruction plots the MCMC samples paths for each entry of the signature matrix P and their exposures, i.e. the E matrix. Only post-burnin paths are available for plotting. Those plots are useful for checking if entries have leveled off, reflecting the sampler convergence.
Paths(signatures$SignExposures)
Each plot shows the entries and exposures of one signature along sampler iterations.
Once the processing is done, the estimated signatures can be displayed in two charts, described below.
Signatures can be visualized in a barplot by issuing the following command:
SignPlot(signatures$SignExposures)
Signatures barplot with error bars reflecting the sample percentiles 0.05, 0.25, 0.75, and 0.95 for each entry.
Estimated signatures can also be visualized in a heatmap, generated by the following command:
SignHeat(signatures$SignExposures)
Heatmap showing the entries of each signature.
The relative contribution of each signature to the inspected genomes can be displayed in several ways. signeR currently provides three alternatives.
The levels of exposure to each signature in all genome samples can also be plotted:
ExposureBoxplot(signatures$SignExposures)
The contribution of the signatures to the mutations found on each genome sample can also be visualized in a barplot, plotted by the following command:
ExposureBarplot(signatures$SignExposures)
Barplot showing the contributions of the signatures to genome samples mutation counts.
The relative contribution of signatures on each genome sample can also be visualized in a barplot, setting the relative parameter to TRUE:
ExposureBarplot(signatures$SignExposures, relative=TRUE)
Barplot showing the relative contributions of signatures to genome samples.
The levels of exposure to each signature can also be plotted in a heatmap:
ExposureHeat(signatures$SignExposures)
Heatmap showing the exposures for each genome sample. Samples are grouped according to their levels of exposure to the signatures, as can be seen in the dendrogram on the left.
If additional information is available for the samples analysed signeR is able to evaluate how those relate with the estimated exposures to mutational signatures. When additional data is categorical, differences in exposures among groups can be analysed and if some of the samples are unlabeled they can be labeled based on the similarity of their exposure profiles to those of labeled samples. In the case of a continuous additional feature, its correlation to estimated exposures can be evaluated. Survival data can also be analysed and the relation of signatures to survival can be accessed. In every case, analyses are repeated for all samples of the exposure matrix generated by signeR sampler and results are considered significant if they are consistently found on most of them.
signeR can highlight signatures that are differentially active among
previously defined groups of samples. To perform this task signeR needs
a vector of group labels. In this example the samples were divided according to
germline mutations at BRCA genes: groups wt,
BRCA1+ and BRCA2+, taken from the description of the
21 breast cancer data set.
# group labels, respective to each row of the mutation count matrix BRCA_labels <- c("wt","BRCA1+","BRCA2+","BRCA1+","BRCA2+","BRCA1+","BRCA1+", "wt","wt","wt","wt","BRCA1+","wt","BRCA2+","BRCA2+","wt","wt","wt", "wt","wt","wt") diff_exposure <- DiffExp(signatures$SignExposures, labels=BRCA_labels)
Top chart: DES plot showing that the BRCA+ samples were significantly more exposed to signatures S3, S4 and S5. Bottom chart: plots showing the significant differences found when groups are compared against each other. These last plots are generated only when there are more than two groups in the analysis and any signature is found to be differentially active. Groups marked by the same letter are not significantly different for the corresponding signature.
The Pvquant vector holds the pvalues quantile of the test for
each signature (by default, the 0.5 quantile, i.e. the median). The logarithms
of those are considered the Differential Exposure Scores (DES). Signatures with
Pvquant values below the cutoff, 0.05 by default, are considered as
differentially exposed.
# pvalues diff_exposure$Pvquant
## [1] 0.7732577405 0.0008188777 0.3970037614
The MostExposed vector contains the name of the group where each
differentially exposed signature showed the highest levels of activity.
# most exposed group diff_exposure$MostExposed
## [1] NA "BRCA1+" NA
signeR can also classify samples based on their exposures to mutational processes. In order to do this, a vector of target labels must be provided to the function ExposureClassify. Samples corresponding to NA values in this vector will be classified according to the similarity of their mutational profiles to the ones of labeled samples. Several classification algorithms are available: k-nearst neighbour (knn), linear vector quantization (lvq), Logistic regressin(logreg), linear discriminant analysis (lda), least absolute shrinkage and selection operator (lasso), naive bayes(nb), support vector machines (svm), random forests (rf) and adaboost (ab). The following example uses the sample labels defined in the DES analysis performed previously.
# note that BRCA_labels [15],[20] and [21] are set to NA BRCA_labels <- c("wt","BRCA+","BRCA+","BRCA+","BRCA+","BRCA+","BRCA+","wt","wt", "wt","wt","BRCA+","wt","BRCA+",NA,"wt","wt","wt","wt",NA,NA) Class <- ExposureClassify(signatures$SignExposures, labels=BRCA_labels, method="knn")
Barplot showing the relative frequencies of assignment of each unlabeled sample to the selected group.
# Final assignments Class$class
## PD4116a PD4199a PD4248a ## "BRCA+" "wt" "wt"
# Relative frequencies of assignment to selected groups Class$freq
## PD4116a PD4199a PD4248a ## 1 1 1
# All assigment frequencies Class$allfreqs
## PD4116a PD4199a PD4248a ## BRCA+ 100 0 0 ## wt 0 100 100
When a continuous feature is available for the samples being analysed, signeR can evaluate its correlation to exposures to mutational signatures. The following command applies the cor.test function to evaluate the correlation of the provided feature and the levels of exposure of each signature:
# feature values, respective to each row of the mutation count matrix. # The feature simulated below will be correlated with exposures to signature 2. myFeature <- (10^6)*Median_exp(signatures$SignExposures)[2,] + rnorm(21,0,1) ExpCorr <- ExposureCorrelation(signatures$SignExposures, feature=myFeature)
P-values boxplot and scatterplots showing the correlations of exposures and the provided feature.
The output ExpCorr will contain a list with two vectors: the estimated correlations of the signatures to the feature and their estimated pvalues.
A continuous feature may also be modeled by its exposures to mutational signatures. The following command applies the glm function to fit a linear model with the provided feature as output of the levels of exposures to mutational signatures:
ExpLM <- ExposureGLM(signatures$SignExposures, feature=myFeature)
P-values boxplot showing the relevance of exposures in final model of provided feature.
If survival data is available for the samples being analysed, signeR can evaluate the effect of exposure on survival. The folowing function performs an independent test for the exposures levels of each mutational signature, as opposed to the Cox regression described in next item. If method = logrank samples are separated according to their exposure and top and bottom groups are compared by the log-rank test. Otherwise, method = cox and a Cox's proportional hazards model is fitted to exposure levels and evaluates their effects upon survival.
# survival times and censoring, respective to each row of the mutation count matrix. #Time is simulated so that it is correlated to exposures to signature 3. critical_sig<-Median_exp(signatures$SignExposures)[2,] probs<-(critical_sig-min(critical_sig))/(max(critical_sig)-min(critical_sig)) su<-as.matrix(data.frame(time=sample(80:150,21,replace=T), status=sapply(probs,function(p){sample(c(0,1),1,prob=c(p,1-p))}))) ExpSurv <- ExposureSurvival(Exposures=signatures$SignExposures, surv=su, method="logrank")
P.values boxplots and plots of survival data comparing, for each signature, samples groups showing top or bottom exposure levels.
ExpSurv.cox <- ExposureSurvival(Exposures=signatures$SignExposures, surv=su, method="cox")
## Warning: There was 1 warning in `mutate()`. ## ℹ In argument: `factor.name = map_chr(coefficient_labels, symbol_substring, ## call_symbols)`. ## Caused by warning: ## ! `as_logical()` is deprecated as of rlang 0.4.0 ## Please use `vctrs::vec_cast()` instead. ## This warning is displayed once every 8 hours.
## Warning: Removed 1 rows containing missing values (`geom_segment()`).
P.values boxplots and forestplot showing the effect of each signature upon survival according to univariate Cox's proportional hazards model.
signeR can also evaluate the combined effect on survival of exposure levels to different signatures. The following command fits Cox's proportional hazards model on exposures. It generates a p-values boxplot and a forestplot (form package forestplot) to show the relevance of each mutational signature to survival.
BRCA_labels <- c("wt","BRCA+","BRCA+","BRCA+","BRCA+","BRCA+","BRCA+", "wt","wt","wt","wt","BRCA+","wt","BRCA+","BRCA+","wt","wt","wt", "wt","wt","wt") ExpSurvMd <- ExposureSurvModel(Exposures=signatures$SignExposures, surv=su, addata=data.frame(as.factor(BRCA_labels)))
## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 1 ; coefficient may be infinite.
## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; 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coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite. ## Warning in coxph.fit(X, Y, istrat, offset, init, control, weights = weights, : ## Loglik converged before variable 4 ; coefficient may be infinite.
## Warning: Removed 1 rows containing missing values (`geom_pointrange()`).
## Warning: Removed 1 rows containing missing values (`geom_segment()`).
## Warning: Removed 2 rows containing missing values (`geom_segment()`).
Forestplot: Cox proportional model p-values and hazard ratios for each signature.
When no addtional information is available for the samples analysed, signeR can search patterns on estimated exposures. Unsupervised analysis can be performed on all generated samples of the exposure matrix and consistent results are reported as significant.
Samples can be hierarquicaly clustered according to their exposures to mutational signatures. The function HClustExp applies R function hclust to each sampled exposure matrix. Dendogram branches consistently found on most of the analyses are reported:
# feature values, respective to each row of the mutation count matrix HCE <- HClustExp(signatures$SignExposures,method.dist="euclidean", method.hclust="average")
Hierarquical structure found on data, each branch showing the frequency of its occurance in the analysis of sampled exposure matrices.
signeR can also perform a Fuzzy clustering of the samples according to their exposures to mutational signatures. The function FuzzyClustExp applies a clustering algorithm (hard or fuzzy) on each sampled exposure matrix and averages the fuzzy memberships degrees of samples to clusters. The number of cluster can be defined by the user (Clim parameter), otherwise different numbers of clusters are tested and the one that maximizes the PBMF index is used (the search algorithm used is similar to the one applied to estimate the number of signatures present in a dataset):
FCE <- FuzzyClustExp(signatures$SignExposures, Clim=c(3,7))
## Evaluating models with the number of groups ranging from 3 to 7, please be patient. ## Testing 3 groups. ## Testing 4 groups. ## Testing 5 groups. ## Testing 6 groups. ## Testing 7 groups. ## Optimum number of groups is 3. Performing final clustering.
Heatmap showing the mean fuzzy memberships degrees of samples to clusters.
The function's output is a list of three elements: the mean matrix of fuzzy memberships degrees of samples to clusters, the full array of all fuzzy memberships degrees found by the analysis of sampled exposure matrices and the matrix of memberships degrees found by the analysis of median exposures of samples to signatures.
citation("signeR")
## To cite package 'signeR' in publications use:
##
## Rafael A. Rosales, Rodrigo D. Drummond, Renan Valieris, Emmanuel
## Dias-Neto, and Israel T. da Silva (2016): signeR: An empirical
## Bayesian approach to mutational signature discovery. Bioinformatics
## September 1, 2016 doi:10.1093/bioinformatics/btw572
##
## A BibTeX entry for LaTeX users is
##
## @Article{,
## title = {signeR: An empirical Bayesian approach to mutational signature discovery.},
## author = {Rafael A. Rosales and Rodrigo D. Drummond and Renan Valieris and Emmanuel Dias-Neto and Israel T. da Silva},
## year = {2016},
## journal = {Bioinformatics},
## doi = {10.1093/bioinformatics/btw572},
## }
OS X users might get compilation errors similar to these:
ld: warning: directory not found for option '-L/usr/local/lib/x86_64'
ld: library not found for -lgfortran
ld: library not found for -lquadmath
This problem arises when the machine is missing gfortran libraries necessary to compile RcppArmadillo and signeR. To install the missing libraries, execute these lines on a terminal:
curl -O http://r.research.att.com/libs/gfortran-4.8.2-darwin13.tar.bz2
sudo tar fvxz gfortran-4.8.2-darwin13.tar.bz2 -C /
For more information see this post and the Rcpp FAQ, section 2.16.
Some packages that signeR depends on requires that 3rd party library headers be installed. If you see errors like:
Error: checking for curl-config... no
Cannot find curl-configIt means you need to install these headers with your package manager. For example on ubuntu:
$ sudo apt-get install libcurl4-openssl-devL. B. Alexandrov, S. Nik-Zainal, D. C. Wedge, P. J. Campbell, and M. R. Stratton. Deciphering Signatures of Mutational Processes Operative in Human Cancer. Cell Reports, 3(1):246-259, Jan. 2013. [ DOI ]
A. Fischer, C. J. Illingworth, P. J. Campbell, and V. Mustonen. EMu: probabilistic inference of mutational processes and their localization in the cancer genome. Genome biology, 14(4):R39, Apr. 2013. [ DOI ]
sessionInfo()
## R version 4.3.0 RC (2023-04-13 r84269) ## Platform: x86_64-pc-linux-gnu (64-bit) ## Running under: Ubuntu 22.04.2 LTS ## ## Matrix products: default ## BLAS: /home/biocbuild/bbs-3.17-bioc/R/lib/libRblas.so ## LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.10.0 ## ## locale: ## [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C ## [3] LC_TIME=en_GB LC_COLLATE=C ## [5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8 ## [7] LC_PAPER=en_US.UTF-8 LC_NAME=C ## [9] LC_ADDRESS=C LC_TELEPHONE=C ## [11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C ## ## time zone: America/New_York ## tzcode source: system (glibc) ## ## attached base packages: ## [1] stats4 stats graphics grDevices utils datasets methods ## [8] base ## ## other attached packages: ## [1] signeR_2.2.1 NMF_0.26 ## [3] bigmemory_4.6.1 cluster_2.1.4 ## [5] rngtools_1.5.2 registry_0.5-1 ## [7] VariantAnnotation_1.46.0 Rsamtools_2.16.0 ## [9] Biostrings_2.68.0 XVector_0.40.0 ## [11] SummarizedExperiment_1.30.1 Biobase_2.60.0 ## [13] GenomicRanges_1.52.0 GenomeInfoDb_1.36.0 ## [15] IRanges_2.34.0 S4Vectors_0.38.1 ## [17] MatrixGenerics_1.12.0 matrixStats_0.63.0 ## [19] BiocGenerics_0.46.0 knitr_1.42 ## ## loaded via a namespace (and not attached): ## [1] splines_4.3.0 later_1.3.1 BiocIO_1.10.0 ## [4] bitops_1.0-7 filelock_1.0.2 tibble_3.2.1 ## [7] pROC_1.18.0 XML_3.99-0.14 rpart_4.1.19 ## [10] lifecycle_1.0.3 rstatix_0.7.2 doParallel_1.0.17 ## [13] globals_0.16.2 lattice_0.21-8 MASS_7.3-59 ## [16] kpeaks_1.1.0 backports_1.4.1 magrittr_2.0.3 ## [19] sass_0.4.5 rmarkdown_2.21 jquerylib_0.1.4 ## [22] yaml_2.3.7 httpuv_1.6.9 cowplot_1.1.1 ## [25] DBI_1.1.3 RColorBrewer_1.1-3 lubridate_1.9.2 ## [28] abind_1.4-5 zlibbioc_1.46.0 purrr_1.0.1 ## [31] RCurl_1.98-1.12 rappdirs_0.3.3 pvclust_2.2-0 ## [34] GenomeInfoDbData_1.2.10 KMsurv_0.1-5 listenv_0.9.0 ## [37] pheatmap_1.0.12 parallelly_1.35.0 codetools_0.2-19 ## [40] DelayedArray_0.26.1 xml2_1.3.4 SuppDists_1.1-9.7 ## [43] tidyselect_1.2.0 shape_1.4.6 farver_2.1.1 ## [46] gmp_0.7-1 shinyWidgets_0.7.6 BiocFileCache_2.8.0 ## [49] GenomicAlignments_1.36.0 jsonlite_1.8.4 e1071_1.7-13 ## [52] ellipsis_0.3.2 survival_3.5-5 iterators_1.0.14 ## [55] foreach_1.5.2 BWStest_0.2.2 tools_4.3.0 ## [58] progress_1.2.2 PMCMRplus_1.9.6 Rcpp_1.0.10 ## [61] glue_1.6.2 gridExtra_2.3 mgcv_1.8-42 ## [64] xfun_0.39 kSamples_1.2-9 dplyr_1.1.2 ## [67] withr_2.5.0 shinydashboard_0.7.2 BiocManager_1.30.20 ## [70] fastmap_1.1.1 fansi_1.0.4 digest_0.6.31 ## [73] timechange_0.2.0 R6_2.5.1 mime_0.12 ## [76] colorspace_2.1-0 biomaRt_2.56.0 RSQLite_2.3.1 ## [79] utf8_1.2.3 tidyr_1.3.0 generics_0.1.3 ## [82] data.table_1.14.8 rtracklayer_1.60.0 class_7.3-21 ## [85] bsplus_0.1.4 prettyunits_1.1.1 httr_1.4.5 ## [88] S4Arrays_1.0.1 pkgconfig_2.0.3 gtable_0.3.3 ## [91] Rmpfr_0.9-2 blob_1.2.4 survMisc_0.5.6 ## [94] htmltools_0.5.5 carData_3.0-5 clue_0.3-64 ## [97] multcompView_0.1-9 scales_1.2.1 png_0.1-8 ## [100] survivalAnalysis_0.3.0 km.ci_0.5-6 bigmemory.sri_0.1.6 ## [103] tzdb_0.3.0 reshape2_1.4.4 rjson_0.2.21 ## [106] uuid_1.1-0 nlme_3.1-162 curl_5.0.0 ## [109] nloptr_2.0.3 zoo_1.8-12 proxy_0.4-27 ## [112] cachem_1.0.8 stringr_1.5.0 parallel_4.3.0 ## [115] shinycssloaders_1.0.0 AnnotationDbi_1.62.1 restfulr_0.0.15 ## [118] pillar_1.9.0 grid_4.3.0 vctrs_0.6.2 ## [121] maxstat_0.7-25 ggpubr_0.6.0 VGAM_1.1-8 ## [124] promises_1.2.0.1 randomForest_4.7-1.1 car_3.1-2 ## [127] dbplyr_2.3.2 lhs_1.1.6 ada_2.0-5 ## [130] xtable_1.8-4 evaluate_0.20 readr_2.1.4 ## [133] GenomicFeatures_1.52.0 mvtnorm_1.1-3 cli_3.6.1 ## [136] compiler_4.3.0 rlang_1.1.1 crayon_1.5.2 ## [139] ppclust_1.1.0 ggsignif_0.6.4 future.apply_1.10.0 ## [142] labeling_0.4.2 survminer_0.4.9 forcats_1.0.0 ## [145] plyr_1.8.8 stringi_1.7.12 gridBase_0.4-7 ## [148] BiocParallel_1.34.0 munsell_0.5.0 glmnet_4.1-7 ## [151] Matrix_1.5-4 inaparc_1.2.0 BSgenome_1.68.0 ## [154] hms_1.1.3 bit64_4.0.5 future_1.32.0 ## [157] ggplot2_3.4.2 KEGGREST_1.40.0 shiny_1.7.4 ## [160] highr_0.10 kknn_1.3.1 exactRankTests_0.8-35 ## [163] broom_1.0.4 igraph_1.4.2 memoise_2.0.1 ## [166] bslib_0.4.2 tidytidbits_0.3.2 bit_4.0.5
print(names(dev.cur()))
## [1] "png"