GTestimate is a scRNA-seq normalization method. In contrast to other methods it uses the Simple Good-Turing estimator for the per cell relative gene expression estimation. Thereby GTestimate can account for the unobserved genes and avoid overestimation of the observed genes. At default settings it serves as a drop-in replacement for Seurat's NormalizeData().
You can install the development version of GTestimate like so:
if (!requireNamespace("devtools", quietly = TRUE))
install.packages("devtools")
if (!requireNamespace("sparseMatrixStats", quietly = TRUE))
devtools::install_github("const-ae/sparseMatrixStats")
devtools::install_github("Martin-Fahrenberger/GTestimate")
This is a basic example of how to use GTestimate to normalize scRNA-seq data in a Seurat workflow.
library(GTestimate)
library(Seurat)
data('pbmc_small')
pbmc_small <- GTestimate(pbmc_small) # Instead of NormalizeData(pbmc_small)
pbmc_small <- FindVariableFeatures(pbmc_small)
pbmc_small <- ScaleData(pbmc_small)
pbmc_small <- RunPCA(pbmc_small)
# and so on
This is a basic example of how to use GTestimate to normalize scRNA-seq data in a SingleCellExperiment workflow using size-factors.
library(GTestimate)
library(Seurat)
library(scran)
data('pbmc_small')
pbmc_sce <- as.SingleCellExperiment(pbmc_small)
pbmc_sce <- computeSumFactors(pbmc_sce)
pbmc_sce <- GTestimate(pbmc_sce, size.factors = sizeFactors(pbmc_sce)) # Instead of logNormCounts(sce)
# and so on
The core implementation of the Simple Good-Turing estimator in C++ has been adapted from Aaron Lun's implementation for the edgeR R-package. His implementation was in turn based on Geoffrey Sampson's C code acessible at https://www.grsampson.net/D_SGT.c