DEsingle
Introduction
DEsingle is an R package for
differential expression (DE) analysis of single-cell RNA-seq
(scRNA-seq) data. It will detect differentially expressed genes
between two groups of cells in a scRNA-seq raw read counts matrix.
DEsingle employs the Zero-Inflated
Negative Binomial model for differential expression analysis. By
estimating the proportion of real and dropout zeros, it not only detects
DE genes at higher accuracy but also subdivides
three types of differential expression with different regulatory and
functional mechanisms.
For more information, please refer to the manuscript by Zhun Miao, Ke Deng, Xiaowo Wang and Xuegong Zhang.
Citation
If you use DEsingle in published
research, please cite:
Zhun Miao, Ke Deng, Xiaowo Wang, Xuegong Zhang (2018). DEsingle for detecting three types of differential expression in single-cell RNA-seq data. Bioinformatics, bty332. 10.1093/bioinformatics/bty332.
Installation
To install DEsingle from Bioconductor:
To install the developmental version from GitHub:
if(!require(devtools)) install.packages("devtools")
devtools::install_github("miaozhun/DEsingle", build_vignettes = TRUE)To load the installed DEsingle in
R:
Input
DEsingle takes two inputs:
counts and group.
The input counts is a scRNA-seq raw read counts
matrix or a SingleCellExperiment
object which contains the read counts matrix. The rows of the matrix are
genes and columns are cells.
The other input group is a vector of factor which
specifies the two groups in the matrix to be compared, corresponding to
the columns in counts.
Test data
Users can load the test data in
DEsingle by
The toy data counts in TestData is a
scRNA-seq read counts matrix which has 200 genes (rows) and 150 cells
(columns).
dim(counts)
#> [1] 200 150
counts[1:6, 1:6]
#> E3.46.3383 E3.51.3425 E3.46.3388 E3.51.3423 E3.46.3382 E3.49.3407
#> BTG4 22 0 12 26 0 0
#> GABRB1 0 0 0 0 0 0
#> IL9 0 0 0 0 0 0
#> TAPBPL 2 0 5 1 0 2
#> KANK4 0 0 0 0 0 0
#> CPSF2 12 0 95 0 5 115The object group in TestData is a vector of
factor which has two levels and equal length to the column number of
counts.
Usage
With read counts matrix input
Here is an example to run DEsingle with
read counts matrix input:
# Load library and the test data for DEsingle
library(DEsingle)
data(TestData)
# Specifying the two groups to be compared
# The sample number in group 1 and group 2 is 50 and 100 respectively
group <- factor(c(rep(1,50), rep(2,100)))
# Detecting the DE genes
results <- DEsingle(counts = counts, group = group)
# Dividing the DE genes into 3 categories at threshold of FDR < 0.05
results.classified <- DEtype(results = results, threshold = 0.05)With SingleCellExperiment input
The SingleCellExperiment
class is a widely used S4 class for storing single-cell genomics data.
DEsingle also could take the
SingleCellExperiment data representation as input.
Here is an example to run DEsingle with
SingleCellExperiment input:
# Load library and the test data for DEsingle
library(DEsingle)
library(SingleCellExperiment)
data(TestData)
# Convert the test data in DEsingle to SingleCellExperiment data representation
sce <- SingleCellExperiment(assays = list(counts = as.matrix(counts)))
# Specifying the two groups to be compared
# The sample number in group 1 and group 2 is 50 and 100 respectively
group <- factor(c(rep(1,50), rep(2,100)))
# Detecting the DE genes with SingleCellExperiment input sce
results <- DEsingle(counts = sce, group = group)
# Dividing the DE genes into 3 categories at threshold of FDR < 0.05
results.classified <- DEtype(results = results, threshold = 0.05)Output
DEtype subdivides the DE genes found by
DEsingle into 3 types: DEs,
DEa and
DEg.
DEsrefers to “different expression status”. It is the type of genes that show significant difference in the proportion of real zeros in the two groups, but do not have significant difference in the other cells.DEais for “differential expression abundance”, which refers to genes that are significantly differentially expressed between the groups without significant difference in the proportion of real zeros.DEgor “general differential expression” refers to genes that have significant difference in both the proportions of real zeros and the expression abundances between the two groups.
The output of DEtype is a matrix containing the DE
analysis results, whose rows are genes and columns contain the following
items:
theta_1,theta_2,mu_1,mu_2,size_1,size_2,prob_1,prob_2: MLE of the zero-inflated negative binomial distribution’s parameters of group 1 and group 2.total_mean_1,total_mean_2: Mean of read counts of group 1 and group 2.foldChange: total_mean_1/total_mean_2.norm_total_mean_1,norm_total_mean_2: Mean of normalized read counts of group 1 and group 2.norm_foldChange: norm_total_mean_1/norm_total_mean_2.chi2LR1: Chi-square statistic for hypothesis testing of H0.pvalue_LR2: P value of hypothesis testing of H20 (Used to determine the type of a DE gene).pvalue_LR3: P value of hypothesis testing of H30 (Used to determine the type of a DE gene).FDR_LR2: Adjusted P value of pvalue_LR2 using Benjamini & Hochberg’s method (Used to determine the type of a DE gene).FDR_LR3: Adjusted P value of pvalue_LR3 using Benjamini & Hochberg’s method (Used to determine the type of a DE gene).pvalue: P value of hypothesis testing of H0 (Used to determine whether a gene is a DE gene).pvalue.adj.FDR: Adjusted P value of H0’s pvalue using Benjamini & Hochberg’s method (Used to determine whether a gene is a DE gene).Remark: Record of abnormal program information.Type: Types of DE genes. DEs represents differential expression status; DEa represents differential expression abundance; DEg represents general differential expression.State: State of DE genes, up represents up-regulated; down represents down-regulated.
To extract the significantly differentially expressed genes from the
output of DEtype (note that the same threshold of
FDR should be used in this step as in DEtype):
# Extract DE genes at threshold of FDR < 0.05
results.sig <- results.classified[results.classified$pvalue.adj.FDR < 0.05, ]To further extract the three types of DE genes separately:
Parallelization
DEsingle integrates parallel computing
function with BiocParallel
package. Users could just set parallel = TRUE in function
DEsingle to enable parallelization and leave the
BPPARAM parameter alone.
# Load library
library(DEsingle)
# Detecting the DE genes in parallelization
results <- DEsingle(counts = counts, group = group, parallel = TRUE)Advanced users could use a BiocParallelParam object from
package BiocParallel to fill in the BPPARAM
parameter to specify the parallel back-end to be used and its
configuration parameters.
For Unix and Mac users
The best choice for Unix and Mac users is to use
MulticoreParam to configure a multicore parallel
back-end:
# Load library
library(DEsingle)
library(BiocParallel)
# Set the parameters and register the back-end to be used
param <- MulticoreParam(workers = 18, progressbar = TRUE)
register(param)
# Detecting the DE genes in parallelization with 18 cores
results <- DEsingle(counts = counts, group = group, parallel = TRUE, BPPARAM = param)For Windows users
For Windows users, use SnowParam to configure a Snow
back-end is a good choice:
# Load library
library(DEsingle)
library(BiocParallel)
# Set the parameters and register the back-end to be used
param <- SnowParam(workers = 8, type = "SOCK", progressbar = TRUE)
register(param)
# Detecting the DE genes in parallelization with 8 cores
results <- DEsingle(counts = counts, group = group, parallel = TRUE, BPPARAM = param)See the Reference
Manual of BiocParallel
package for more details of the BiocParallelParam
class.
Visualization of results
Users could use the heatmap() function in
stats or heatmap.2 function in
gplots to plot the heatmap of the DE genes DEsingle found,
as we did in Figure S3 of the manuscript.
Interpretation of results
For the interpretation of results when
DEsingle applied to real data, please
refer to the Three types of DE genes between E3 and E4 of human
embryonic cells part in the Supplementary
Materials of our manuscript.
Help
Use browseVignettes("DEsingle") to see the vignettes of
DEsingle in R after installation.
Use the following code in R to get access to the help documentation
for DEsingle:
You are also welcome to view and post DEsingle tagged questions on Bioconductor Support Site of DEsingle or contact the author by email for help.
Session info
sessionInfo()
#> R version 4.4.1 (2024-06-14)
#> Platform: x86_64-pc-linux-gnu
#> Running under: Ubuntu 24.04.1 LTS
#>
#> Matrix products: default
#> BLAS: /usr/lib/x86_64-linux-gnu/openblas-pthread/libblas.so.3
#> LAPACK: /usr/lib/x86_64-linux-gnu/openblas-pthread/libopenblasp-r0.3.26.so; LAPACK version 3.12.0
#>
#> locale:
#> [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
#> [3] LC_TIME=en_US.UTF-8 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: Etc/UTC
#> tzcode source: system (glibc)
#>
#> attached base packages:
#> [1] stats graphics grDevices utils datasets methods base
#>
#> other attached packages:
#> [1] DEsingle_1.27.0
#>
#> loaded via a namespace (and not attached):
#> [1] gamlss.dist_6.1-1 Matrix_1.7-1 jsonlite_1.8.9
#> [4] compiler_4.4.1 gamlss_5.4-22 parallel_4.4.1
#> [7] VGAM_1.1-12 jquerylib_0.1.4 splines_4.4.1
#> [10] BiocParallel_1.39.0 yaml_2.3.10 fastmap_1.2.0
#> [13] lattice_0.22-6 R6_2.5.1 maxLik_1.5-2.1
#> [16] generics_0.1.3 bbmle_1.0.25.1 knitr_1.48
#> [19] MASS_7.3-61 bdsmatrix_1.3-7 maketools_1.3.1
#> [22] bslib_0.8.0 rlang_1.1.4 cachem_1.1.0
#> [25] gamlss.data_6.0-6 xfun_0.48 sass_0.4.9
#> [28] sys_3.4.3 cli_3.6.3 digest_0.6.37
#> [31] grid_4.4.1 mvtnorm_1.3-1 sandwich_3.1-1
#> [34] lifecycle_1.0.4 nlme_3.1-166 miscTools_0.6-28
#> [37] pscl_1.5.9 evaluate_1.0.1 numDeriv_2016.8-1.1
#> [40] zoo_1.8-12 codetools_0.2-20 buildtools_1.0.0
#> [43] survival_3.7-0 stats4_4.4.1 rmarkdown_2.28
#> [46] tools_4.4.1 htmltools_0.5.8.1