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RESOLVE

This is the released version of RESOLVE; for the devel version, see RESOLVE.

All versions 3.24 (devel), 3.23 (release), 3.22, 3.21, 3.20, 3.19, 3.18, 3.17, 3.16

RESOLVE: An R package for the efficient analysis of mutational signatures from cancer genomes


Bioconductor version: Release (3.23)

Cancer is a genetic disease caused by somatic mutations in genes controlling key biological functions such as cellular growth and division. Such mutations may arise both through cell-intrinsic and exogenous processes, generating characteristic mutational patterns over the genome named mutational signatures. The study of mutational signatures have become a standard component of modern genomics studies, since it can reveal which (environmental and endogenous) mutagenic processes are active in a tumor, and may highlight markers for therapeutic response. Mutational signatures computational analysis presents many pitfalls. First, the task of determining the number of signatures is very complex and depends on heuristics. Second, several signatures have no clear etiology, casting doubt on them being computational artifacts rather than due to mutagenic processes. Last, approaches for signatures assignment are greatly influenced by the set of signatures used for the analysis. To overcome these limitations, we developed RESOLVE (Robust EStimation Of mutationaL signatures Via rEgularization), a framework that allows the efficient extraction and assignment of mutational signatures. RESOLVE implements a novel algorithm that enables (i) the efficient extraction, (ii) exposure estimation, and (iii) confidence assessment during the computational inference of mutational signatures.

Author: Daniele Ramazzotti [aut] ORCID iD ORCID: 0000-0002-6087-2666 , Luca De Sano [cre, aut] ORCID iD ORCID: 0000-0002-9618-3774

Maintainer: Luca De Sano <luca.desano at gmail.com>

Citation (from within R, enter citation("RESOLVE")):

Daniele Ramazzotti, Luca De Sano. RESOLVE: RESOLVE: An R package for the efficient analysis of mutational signatures from cancer genomes. doi:10.18129/B9.bioc.RESOLVE, R package version 1.14.0, https://bioconductor.org/packages/RESOLVE.

Generated from the package metadata; it may differ from the package's own citation.

Installation

To install this package, start R (version "4.6") and enter:

if (!require("BiocManager", quietly = TRUE))
    install.packages("BiocManager")

BiocManager::install("RESOLVE")

For older versions of R, please refer to the appropriate Bioconductor release.

Documentation

To view documentation for the version of this package installed in your system, start R and enter:

browseVignettes("RESOLVE")
RESOLVE.html HTML R Script
Reference ManualPDF
NEWSText
LICENSEText

Details

biocViews BiomedicalInformatics, Software, SomaticMutation
Version1.14.0
In Bioconductor sinceBioC 3.16 (R-4.2) (4 years)
License file LICENSE
Depends R (>= 4.1.0)
Imports Biostrings, BSgenome, BSgenome.Hsapiens.1000genomes.hs37d5, cluster, data.table, GenomeInfoDb, GenomicRanges, glmnet, ggplot2, gridExtra, IRanges, lsa, MutationalPatterns, nnls, parallel, reshape2, S4Vectors, RhpcBLASctl, survival
System Requirements
URLhttps://github.com/danro9685/RESOLVE
Bug Reportshttps://github.com/danro9685/RESOLVE/issues
See More
Suggests BiocGenerics, BiocStyle, testthat, knitr
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Depends On Me
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Build Report Build Report, r-universe

Package Archives

Follow Installation instructions to use this package in your R session.

Source Package RESOLVE_1.14.0.tar.gz
Windows Binary (x86_64) RESOLVE_1.14.0.zip
macOS Binary (big-sur-x86_64) RESOLVE_1.14.0.tgz
macOS Binary (sonoma-arm64) RESOLVE_1.14.0.tgz
Source Repositorygit clone https://git.bioconductor.org/packages/RESOLVE
Source Repository (Developer Access)git clone git@git.bioconductor.org:packages/RESOLVE
Package Short Url https://bioconductor.org/packages/RESOLVE/
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