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# singscore <img src="" alt="logo" align="right" height="140" width="120"/> [![R-CMD-check](]( [![codecov](]( [![BioC status](]( ## Overview ‘singscore’ is an R/Bioconductor package which implements the simple single-sample gene-set (or gene-signature) scoring method proposed by Foroutan *et al.* (2018) and Bhuva *et al.* (2020). It uses rank-based statistics to analyze each sample’s gene expression profile and scores the expression activities of gene sets at a single-sample level. Additional packages we have developed can enhance the singscore workflow: 1. [`msigdb`]( - A package that provides gene-sets from the molecular signatures database (MSigDB) as a `GeneSetCollection` object that is compatible with `singscore`. 2. [`vissE`]( - A package that can summarise and aid in the interpretation of a list of significant gene-sets identified by `singscore` (see [tutorial]( 3. [`emtdata`]( - The full EMT dataset used in this tutorial (with additional EMT related datasets). We have also published and made openly available the extensive tutorials below that demonstrate the variety of ways in which `singscore` can be used to gain a better functional understanding of molecular data: 1. [Using singscore to predict mutation status in acute myeloid leukemia from transcriptomic signatures]( 2. [Gene-set enrichment analysis workshop]( - available through the [Orchestra]( platform (search “WEHI Masterclass Day 4: Functional Analysis, single sample gene set analysis”). ## Getting Started These instructions will get you to install the package up and running on your local machine. If you experience any issues, please raise a GitHub issue at <>. # build_vignettes = TRUE to build vignettes upon installation if (!requireNamespace("BiocManager", quietly = TRUE)) install.packages("BiocManager") BiocManager::install("singscore", version = "3.8") ## Documentation The package comes with a vignette showing how the different functions in the package can be used to perform a gene-set enrichment analysis on a single sample level. Pre-built vignettes can be accessed via [Bioconductor]( or [the GitHub IO page]( ## References Foroutan M, Bhuva D, Lyu R, Horan K, Cursons J, Davis M (2018). “Single sample scoring of molecular phenotypes.” *BMC bioinformatics*, *19*(1), 404. doi: [10.1186/s12859-018-2435-4]( Bhuva D, Cursons J, Davis M (2020). “Stable gene expression for normalisation and single-sample scoring.” *Nucleic Acids Research*, *48*(19), e113. doi: [10.1093/nar/gkaa802](