In UMCUGenetics/mutSigExtractor: Extracts SNV, indel, DBS, and SV signatures from vcf files.

Description

mutSigExtractor is an R package for extracting mutation contexts from vcf files. Extraction can be performed for the following mutation types:

• SNV: 96 trinucleotide contexts, consisting of the point mutation and the 5' and 3' flanking nucleotides
• DBS: 78 possible double base substitution types
• Indel: Includes indels within repeat regions, indels with flanking microhomology; and other indels. Each category is further stratified by the repeat unit length, the number of bases in the indel sequence that are homologous, and the indel sequence length, respectively. Alternatively, the PCAWG indel contexts can also be extracted
• SV: structural variants stratified by type (deletions, duplications, inversions, translocations) and length (0 to >10Mb)

Signatures can also be extracted from these contexts for SNVs, indels, DBSs (COSMIC/PCAWG), as well as for SVs (Nik-Zainal et al. 2016).

Installation

mutSigExtractor requires some bioconductor packages to first be installed.

## Bioconductor packages required by mutSigExtractor
install.packages('BiocManager')
BiocManager::install('BSgenome') ## Install genome parser
BiocManager::install('BSgenome.Hsapiens.UCSC.hg19') ## Install the default genome
BiocManager::install('GenomeInfoDb')

## Install mutSigExtractor directly from github using devtools
install.packages("devtools")
devtools::install_github('https://github.com/UMCUGenetics/mutSigExtractor/')

Other genomes (e.g. for hg38: BSgenome.Hsapiens.UCSC.hg38) can also be used. Please see the below tutorial for details.

Tutorial

The COLO829v003T.purple.somatic.vcf.gz and COLO829v003T.purple.sv.vcf.gz files in doc/vcf/ will be used to demonstrate how to use mutSigExtractor.

pkg_dir <- '/Users/lnguyen/hpc/cuppen/projects/P0013_WGS_patterns_Diagn/CHORD/processed/scripts_main/mutSigExtractor/'
devtools::load_all(pkg_dir)
vcf_snv <- paste0(pkg_dir, '/doc/vcf/COLO829v003T.purple.somatic.vcf.gz')
vcf_sv <- paste0(pkg_dir,'/doc/vcf/COLO829v003T.purple.sv.vcf.gz')

setwd('/path/to/mutSigExtractor')
vcf_snv <- 'doc/vcf/COLO829v003T.purple.somatic.vcf.gz'
vcf_sv <- 'doc/vcf/COLO829v003T.purple.sv.vcf.gz'

The main functions for extracting signatures are:

extractSigsSnv()
extractSigsDbs()
extractSigsIndel()
extractSigsSv()

Note that SNVs, DBSs and indels are often reported in the same vcf file. Therefore, extractSigsSnv(),extractSigsDbs(), and extractSigsIndel() will automatically select the relevant mutation types.

Extracting contexts and signatures

SNVs

Here, extraction of SNV contexts and signatures on one sample using extractSigsSnv() will be demonstrated. The same concepts shown here can be applied to the other mutation type functions.

With the below code we can extract the 96 trinucleotide contexts. This returns a single column matrix of mutation counts per context.

Why is the output not simply a vector? This is so that the output can be written to a txt file, which is useful when processing a large number of samples on an HPC. When processing multiple samples locally, one can simply use cbind() combine the context counts from all samples into one matrix.

Note that, it is recommended that the vcf.filter argument is set to 'PASS' (or '.' for certain vcf files) to remove low quality variants.

contexts_snv <- extractSigsSnv(vcf.file=vcf_snv, vcf.filter='PASS', output='contexts')
head(contexts_snv)

To extract signatures, we can then fit these contexts to e.g. the COSMIC or PCAWG signature profiles. These are included in the package as SBS_SIGNATURE_PROFILES_V2 and SBS_SIGNATURE_PROFILES_V3 respectively. For this example we will use the PCAWG profiles (SBS_SIGNATURE_PROFILES_V3).

SBS_SIGNATURE_PROFILES_V3[1:5,1:5]

Signature fitting is done using fitToSignatures() This function uses the non-negative linear least squares algorithm based on lsqnonneq() from the pracma package. mut.context.counts can be a numeric vector, matrix, or dataframe. If a matrix/dataframe, rows represent samples and columns represent contexts.

sigs_snv <- fitToSignatures(
   mut.context.counts=contexts_snv[,1], 
   signature.profiles=SBS_SIGNATURE_PROFILES_V3
)
head(sigs_snv)

Alternatively, signatures can be extracted directly from the vcf by specifying output='signatures' in extractSigsSnv()

sig_snv_2 <- extractSigsSnv(
   vcf.file=vcf_snv, vcf.filter='PASS', output='signatures', 
   signature.profiles=SBS_SIGNATURE_PROFILES_V3
)
head(sig_snv_2)

Output contexts for DBSs, indels, and SVs

The context extractions for mutation types other than SNVs are shown below.

DBSs

contexts_dbs <- extractSigsDbs(vcf.file=vcf_snv, vcf.filter='PASS', output='contexts')
head(contexts_dbs)

Indels

For indels, extractSigsIndel() defaults to method='CHORD' which is used by Classifier of HOmologous Recombination Deficiency (CHORD). When method='CHORD', contexts are always extracted (i.e. no output argument).

contexts_indel <- extractSigsIndel(vcf.file=vcf_snv, vcf.filter='PASS')
head(contexts_indel)

However, the PCAWG indel contexts can also be extracted by setting method='PCAWG'. Here, output can be 'signatures' to directly extract the PCAWG indel signatures.

contexts_indel <- extractSigsIndel(vcf.file=vcf_snv, vcf.filter='PASS', method='PCAWG', output='contexts')
head(contexts_indel)

SVs

SV vcf files generally do not adhere to one standard. extractSigsSv() currently supports SV vcf parsing of GRIDSS (conforms to vcf spec 4.2) and Manta vcfs. You can specify the vcf type with sv.caller='gridss' (default) or sv.caller='manta'.

contexts_sv <- extractSigsSv(vcf.file=vcf_sv, vcf.filter='PASS', output='contexts', sv.caller='gridss')
head(contexts_sv)

In case you want to use SV vcfs from other callers, you can provide a dataframe as input to extractSigsSv() containing SV type and length info. See below for more info.

Dataframes as input

Alternatively, dataframes can be used as input, which is handy if you want to parse the vcfs yourself, or have inputs in tabular format.

For SNVs and indels, a dataframe with the columns: chrom, pos, ref, alt.

##   CHROM      POS REF ALT
## 1     1 16145827   A   C
## 2     1 16492085   G   C
## 3     1 17890303   C   G
## 4     1 18877885   G   A
## 5     1 18919776   T   C

For SVs, a dataframe with the columns: sv_type, sv_len. For sv_type, values must be DEL, DUP, INV, TRA (deletions, duplications, inversions, translocations). For translocations, sv_len information is discarded. The column names themselves do not matter, as long as the columns are in the aforementioned order.

##   sv_type    sv_len
## 1     TRA        NA
## 2     DEL      1696
## 3     DEL     22644
## 4     DUP      1703
## 5     DEL      1789
## 6     DEL     49256

These dataframe can be provided to the extractSigs* functions using the argument df. For example:

extractSigsSv(df=sv_dataframe, vcf.filter='PASS', output='contexts', sv.caller='gridss')

Available signature profiles

Below is a summary of the signature profiles pre-loaded within mutSigExtractor

• SBS_SIGNATURE_PROFILES_V2: Original 30 SNV signatures
• SBS_SIGNATURE_PROFILES_V3: PCAWG SNV signatures
• INDEL_SIGNATURE_PROFILES: PCAWG indel signatures
• DBS_SIGNATURE_PROFILES: PCAWG DBS signatures
• SV_SIGNATURE_PROFILES: SV signatures from Nik-Zainal et al. 2016 with clustered SV information removed

Using other reference genomes

A different reference genome than the default (BSgenome.Hsapiens.UCSC.hg19) can be used. Genomes should be BSgenomes. The variable name (i.e. no quotes) of the BSgenome object is specified to ref.genome.

## Make sure to install and load the desired ref genome first
install.packages('BiocManager')
BiocManager::install('BSgenome.Hsapiens.UCSC.hg38')

## Non-default genomes need to be explicitly loaded. The default (BSgenome.Hsapiens.UCSC.hg19)
## is automatically loaded.
library(BSgenome.Hsapiens.UCSC.hg38)

## Specify the name of the BSgenome object to the ref.genome argument
extractSigsSnv(
  vcf.file='/path/to/vcf/with/snvs_and_indels/', vcf.filter='PASS', output='contexts',
  ref.genome=BSgenome.Hsapiens.UCSC.hg38
)

UMCUGenetics/mutSigExtractor documentation built on Aug. 30, 2024, 2:12 p.m.