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Yue Pan 19 April, 2022
The R package ‘scpoisson’ is developed to visualize the Poissoneity of scRNA-seq data, and explore cell clustering based on model departure as a novel data representation.
Please install from bitbucket repository “dittmerlab/scpoisson”.
remotes::install_bitbucket("dittmerlab/scpoisson")library(scpoisson)
library(magrittr)
library(purrr)##
## Attaching package: 'purrr'
## The following object is masked from 'package:magrittr':
##
## set_namesThe examples below show Q-Q envelope plots comparing sample data with a theoretical Poisson distribution given the Poisson parameter (mean). The input can be either a numeric vector or a numeric matrix consists of integers. If the input is a numeric matrix, the GLM-PCA algorithm will be applied for parameter estimation. Then some matrix entries (default 200, with estimated Poisson parameters closest to the given Poisson parameter) will be selected as sample data and compare with the theoretical distribution. If the theoretical distribution fits the sample data well, the quantile points (or line) will approximately lie on the diagonal line, and also within the envelope.
The code here is specific for validation of independent Poisson distributions, but such idea can be applied to different types of data under different assumptions of distributions.
# Numeric vector as input
set.seed(1234)
scppp_obj <- scppp(rpois(200, 3))
qqplot_env_pois(scppp_obj, 3, 100)
# Count matrix as input
set.seed(1234)
dat <- matrix(c(rpois(300, 5), rpois(200, 1)), ncol = 20)
scppp_obj <- scppp(dat)
qqplot_env_pois(scppp_obj, L = 2, lambda = 5) # small L for a data with less variance
Please refer to vignette for a more detailed guide, including the application in the real data.
The example below shows Hclust-Depart clustering pipeline based on based on model departure using a simplified two-cluster simulated data. The results will be saved in a list. The first element contains the clustering results for each sample, where the cluster label shows the top-down cluster in a tree structure. E.g. Both cluster ‘1-1’ and cluster ‘1-2’ are subclusters from cluster ‘1’ after first split; while cluster ‘1-1’ and cluster ‘2-1’ come from different cluster after first split. The second element is a matrix with samples/cells as rows and cluster index as columns, where each entry contains the hypothesis testing p-value corresponding to each cluster at each split step (each cell within the that cluster will have the same p-value).
This simplified example only contains two clusters, with cluster label either ‘1’ or ‘2’.
set.seed(1234)
para1 <- matrix(c(rep(2L, 20), rep(1L, 40)), ncol = 1)
para2 <- matrix(c(rep(2L, 10), rep(1L, 20)), nrow = 1)
dat <- para1 %*% para2
dat[31:60, 1:10] <- dat[31:60, 1:10] + 10L
counts <- map_int(dat, ~rpois(1, .x)) %>%
matrix(ncol = 30)
colnames(counts) <- paste0("cell", 1:30)
rownames(counts) <- paste0("gene", 1:60)
scppp_obj <- scppp(counts)
heatmap(scppp_obj[["data"]])
scppp_obj <- HclustDepart(scppp_obj, maxSplit = 3)
# cluster results for each cell after each split
head(scppp_obj[["clust_results"]]$Hclust[[1]])## names cluster
## 1 cell1 1
## 2 cell2 1
## 3 cell3 1
## 4 cell4 1
## 5 cell5 1
## 6 cell6 1# p-value for each cell after each split
head(scppp_obj[["clust_results"]]$Hclust[[2]])## [,1] [,2] [,3]
## [1,] 0.02274 NA NA
## [2,] 0.02274 NA NA
## [3,] 0.02274 NA NA
## [4,] 0.02274 NA NA
## [5,] 0.02274 NA NA
## [6,] 0.02274 NA NAPlease refer to vignette for a more detailed guide, including the application in the real data.
Another option is: keep model departure as data representation but apply the Louvain algorithm (implemented in Seurat pipeline) for clustering.
scppp_obj <- LouvainDepart(scppp_obj)## Modularity Optimizer version 1.3.0 by Ludo Waltman and Nees Jan van Eck
##
## Number of nodes: 30
## Number of edges: 435
##
## Running Louvain algorithm...
## Maximum modularity in 10 random starts: 0.2517
## Number of communities: 2
## Elapsed time: 0 secondshead(scppp_obj[["clust_results"]]$Lclust[[4]])## names cluster
## cell1 cell1 1
## cell2 cell2 1
## cell3 cell3 1
## cell4 cell4 1
## cell5 cell5 1
## cell6 cell6 1In this simple case, both clustering pipeline give the same clustering results as we expected.
We can find differentially expressed genes between two clusters based on model departure. Run ‘adj_CDF_logit’ function first to calculate the departure representation. The cluster labels for such comparison need to match the output from Hclust-Depart clustering. The genes in the output will be ranked by decreasing order of mean difference between two clusters.
scppp_obj <- adj_CDF_logit(scppp_obj)
scppp_obj <- diff_gene_list(scppp_obj, clust1 = "1", clust2 = "2", t = F)
head(scppp_obj[["de_results"]]$Hclust)## variable clust1_mean clust2_mean clust1_n clust2_n mean_diff statistic
## 1 gene42 1.145131 -1.346082 10 20 2.491212 177
## 2 gene39 1.107470 -1.314327 10 20 2.421796 183
## 3 gene48 1.098889 -1.291513 10 20 2.390401 184
## 4 gene53 1.048909 -1.245737 10 20 2.294646 175
## 5 gene58 1.044325 -1.250291 10 20 2.294616 166
## 6 gene52 1.042028 -1.244017 10 20 2.286046 181
## p.value padj abs_diff
## 1 0.0007587375 0.002845266 2.491212
## 2 0.0002830659 0.001887106 2.421796
## 3 0.0002369525 0.001777144 2.390401
## 4 0.0010403270 0.002851969 2.294646
## 5 0.0039363264 0.007618696 2.294616
## 6 0.0003972232 0.002018305 2.286046Please report any issues at bitbucket repository.
Townes, F. W., Hicks, S. C., Aryee, M. J., & Irizarry, R. A. (2019). Feature selection and dimension reduction for single-cell RNA-Seq based on a multinomial model. Genome biology, 20(1), 1-16.
Stuart T, Butler A, Hoffman P, Hafemeister C, Papalexi E, III WMM, Hao Y, Stoeckius M, Smibert P, Satija R (2019). “Comprehensive Integration of Single-Cell Data.” Cell, 177, 1888-1902. doi: 10.1016/j.cell.2019.05.031, https://doi.org/10.1016/j.cell.2019.05.031.
These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.