Visualize and interpret topics in PBMC data
Peter Carbonetto
Last updated: 2020-08-23
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Knit directory: single-cell-topics/analysis/
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| File | Version | Author | Date | Message |
|---|---|---|---|---|
| Rmd | 005b217 | Peter Carbonetto | 2020-08-23 | workflowr::wflow_publish(“plots_pbmc.Rmd”) |
| html | 59777e7 | Peter Carbonetto | 2020-08-22 | Added table comparing Zheng et al (2017) labeling with clusters in |
| Rmd | 9cd4a08 | Peter Carbonetto | 2020-08-22 | workflowr::wflow_publish(“plots_pbmc.Rmd”) |
| html | c87ddf8 | Peter Carbonetto | 2020-08-22 | Added PBMC purified structure plot with the new clustering (A1, A2, B, |
| Rmd | c6dd5f2 | Peter Carbonetto | 2020-08-22 | workflowr::wflow_publish(“plots_pbmc.Rmd”) |
| html | ce421ae | Peter Carbonetto | 2020-08-22 | A few small revisions to plots_pbmc analysis. |
| Rmd | ddc6de4 | Peter Carbonetto | 2020-08-22 | workflowr::wflow_publish(“plots_pbmc.Rmd”) |
| html | a406a2f | Peter Carbonetto | 2020-08-22 | Added back first PCA plot for 68k pbmc data. |
| Rmd | 8daa131 | Peter Carbonetto | 2020-08-22 | workflowr::wflow_publish(“plots_pbmc.Rmd”) |
| html | 7900d17 | Peter Carbonetto | 2020-08-22 | Revamping the process of defining clusters in plots_pbmc using PCA. |
| Rmd | 14dd774 | Peter Carbonetto | 2020-08-22 | workflowr::wflow_publish(“plots_pbmc.Rmd”) |
| Rmd | 944ce0c | Peter Carbonetto | 2020-08-22 | Working on new PCA plots for purified PBMC c3 subclusters. |
| html | b05232d | Peter Carbonetto | 2020-08-22 | Build site. |
| Rmd | d0e9f6e | Peter Carbonetto | 2020-08-22 | workflowr::wflow_publish(“plots_pbmc.Rmd”) |
| html | fbb0697 | Peter Carbonetto | 2020-08-21 | Build site. |
| Rmd | cdca13e | Peter Carbonetto | 2020-08-21 | workflowr::wflow_publish(“plots_pbmc.Rmd”) |
| html | 216027a | Peter Carbonetto | 2020-08-21 | Re-built plots_pbmc webpage with structure plots. |
| Rmd | 98888b2 | Peter Carbonetto | 2020-08-21 | Added structure plots to plots_pbmc.R. |
| html | 9310993 | Peter Carbonetto | 2020-08-21 | Revised the PCA plots in pbmc_plots. |
| Rmd | 3a746ff | Peter Carbonetto | 2020-08-21 | workflowr::wflow_publish(“plots_pbmc.Rmd”) |
| Rmd | 1091dd0 | Peter Carbonetto | 2020-08-21 | Added code for Ternary plots to plots_pbmc. |
| html | 6d3d7e4 | Peter Carbonetto | 2020-08-20 | Added 68k PCA plots to plots_pbmc. |
| Rmd | 6ec82ca | Peter Carbonetto | 2020-08-20 | workflowr::wflow_publish(“plots_pbmc.Rmd”) |
| html | 38f07a2 | Peter Carbonetto | 2020-08-20 | A few small revisions to the plots_pbmc analysis. |
| Rmd | fd0316f | Peter Carbonetto | 2020-08-20 | workflowr::wflow_publish(“plots_pbmc.Rmd”) |
| html | 606cd97 | Peter Carbonetto | 2020-08-20 | Added basic PCA plots to plots_pbmc. |
| Rmd | 1b41a60 | Peter Carbonetto | 2020-08-20 | workflowr::wflow_publish(“plots_pbmc.Rmd”) |
| html | d6e5d39 | Peter Carbonetto | 2020-08-20 | Added PCA plot with purified PBMC clustering to plots_pbmc analysis. |
| Rmd | 99301a7 | Peter Carbonetto | 2020-08-20 | workflowr::wflow_publish(“plots_pbmc.Rmd”) |
| Rmd | bf23ca0 | Peter Carbonetto | 2020-08-20 | Added manual labeling of purified PBMC data to plots_pbmc analysis. |
| html | 0c1b570 | Peter Carbonetto | 2020-08-20 | First build on plots_pbmc page. |
| Rmd | eb7f776 | Peter Carbonetto | 2020-08-20 | workflowr::wflow_publish(“plots_pbmc.Rmd”) |
TO DO: Add introductory text here.
Load the packages used in the analysis below.
library(dplyr)
library(fastTopics)
library(ggplot2)
library(cowplot)
library(Ternary)
source("../code/plots.R")Load the sample annotations. (The count data are no longer needed at this stage of the analysis, so I have removed them.)
load("../data/pbmc_purified.RData")
samples_purified <- samples
load("../data/pbmc_68k.RData")
samples_68k <- samples
rm(genes,counts)Load the \(k = 6\) Poisson NMF model fits for both PBMC data sets. In the descriptions below, I refer to these Poisson NMF model fits as the “purified” and “68k” fits.
To aid presentation of the results, topics in the 68k fit are reordered to better align with the topics in purified Poisson NMF fit.
fit_purified <-
readRDS("../output/pbmc-purified/rds/fit-pbmc-purified-scd-ex-k=6.rds")$fit
fit_68k <- readRDS("../output/pbmc-68k/rds/fit-pbmc-68k-scd-ex-k=6.rds")$fit
cols <- c(4,1,5,3,6,2)
fit_68k$F <- fit_68k$F[,cols]
fit_68k$L <- fit_68k$L[,cols]
colnames(fit_68k$F) <- paste0("k",1:6)
colnames(fit_68k$L) <- paste0("k",1:6)We begin by exploring structure in the data as inferred by the topic model. We will visualize this structure by plotting principal components (PCs) of the topic proportions. Although PCA is simple, we will see that it quite effective, and avoids the complications of nonlinear dimensionality reduction techniques such as t-SNE and UMAP.
We begin with the mixture of FACS-purified PBMC data.
fit <- poisson2multinom(fit_purified)
pca <- prcomp(fit$L)$xThree large clusters are clearly evident from first two PCs (there is also finer-scale structure which we will examine shortly). We label these clusters as “A”, “B” and “C”.
n <- nrow(pca)
x <- rep("C",n)
pc1 <- pca[,"PC1"]
pc2 <- pca[,"PC2"]
x[pc1 + 0.2 > pc2] <- "A"
x[pc2 > 0.25] <- "B"
x[(pc1 + 0.4)^2 + (pc2 + 0.1)^2 < 0.07] <- "C"
samples_purified$cluster <- x
p1 <- pca_plot_with_labels(fit_purified,c("PC1","PC2"),
samples_purified$cluster) +
labs(fill = "cluster")
print(p1)
Most of the samples are in cluster A:
table(x)
# x
# A B C
# 72614 10439 11602In cluster C, there are two well-defined subclusters, labeled “C1” and “C2”. There are other possible subclusters that are less defined, but here we focus on the most obvious clustering:
rows <- which(samples_purified$cluster == "C")
fit <- select(poisson2multinom(fit_purified),loadings = rows)
pca <- prcomp(fit$L)$x
n <- nrow(pca)
x <- rep("C3",n)
pc1 <- pca[,1]
pc2 <- pca[,2]
x[pc1 < 0 & pc2 < 0.4] <- "C1"
x[pc1 > 0.5 & pc2 < 0.3] <- "C2"
samples_purified$cluster[rows] <- x
p5 <- pca_plot_with_labels(fit,c("PC1","PC2"),x) +
labs(fill = "cluster")
print(p5)
| Version | Author | Date |
|---|---|---|
| 7900d17 | Peter Carbonetto | 2020-08-22 |
The two subclusters C1 and C2 account for most of the samples:
table(x)
# x
# C1 C2 C3
# 7822 2990 790Let’s now look more closely at cluster A. There is a large, much less distinct subcluster, which we label as “A1”. Otherwise, there are no other clearly well-defined clusters.
rows <- which(samples_purified$cluster == "A")
fit <- select(poisson2multinom(fit_purified),loadings = rows)
pca <- prcomp(fit$L)$x
n <- nrow(fit$L)
x <- rep("A2",n)
pc1 <- pca[,1]
pc2 <- pca[,2]
x[pc1 > 0.58 - pc2 | pc1 > 0.7] <- "A1"
samples_purified$cluster[rows] <- x
p6 <- pca_plot_with_labels(fit,c("PC1","PC2"),x) +
labs(fill = "cluster")
print(p6)
| Version | Author | Date |
|---|---|---|
| 7900d17 | Peter Carbonetto | 2020-08-22 |
In summary, we have subdivided these data into 6 clusters:
samples_purified$cluster <- factor(samples_purified$cluster)
table(samples_purified$cluster)
#
# A1 A2 B C1 C2 C3
# 8271 64343 10439 7822 2990 790The Structure plot gives a compact visual summary of topic proportions in each of these six clusters:
set.seed(1)
pbmc_purified_topics <- c(2,5,1,3,4,6)
pbmc_purified_topic_colors <- c("gold","forestgreen","dodgerblue",
"gray","greenyellow","magenta")
rows <- sort(c(sample(which(samples_purified$cluster == "A1"),250),
sample(which(samples_purified$cluster == "A2"),750),
sample(which(samples_purified$cluster == "B"),250),
sample(which(samples_purified$cluster == "C1"),250),
sample(which(samples_purified$cluster == "C2"),250),
sample(which(samples_purified$cluster == "C3"),200)))
p3 <- structure_plot(select(poisson2multinom(fit_purified),loadings = rows),
grouping = samples_purified[rows,"cluster"],
topics = pbmc_purified_topics,
colors = pbmc_purified_topic_colors[pbmc_purified_topics],
gap = 40,num_threads = 4,verbose = FALSE)
print(p3)
Compare these clusters with the Zheng et al (2017) cell-type labeling:
with(samples_purified,table(celltype,cluster))
# cluster
# celltype A1 A2 B C1 C2 C3
# CD19+ B 0 3 10073 0 1 8
# CD14+ Monocyte 0 30 8 1 2443 130
# CD34+ 4 43 352 7740 545 548
# CD4+ T Helper2 1 11183 0 16 0 13
# CD56+ NK 8243 120 0 17 1 4
# CD8+ Cytotoxic T 21 10135 0 0 0 53
# CD4+/CD45RO+ Memory 0 10201 0 19 0 4
# CD8+/CD45RA+ Naive Cytotoxic 1 11945 3 0 0 4
# CD4+/CD45RA+/CD25- Naive T 1 10440 1 25 0 12
# CD4+/CD25 T Reg 0 10243 2 4 0 14Next, we turn to the 68k fit.
fit <- poisson2multinom(fit_68k)
pca <- prcomp(fit$L)$xIn this case, we find least three distinct clusters in the projection onto PCs 3 and 4. We label these clusters “A”, “B” and “C”, as above, but this labeling does not imply a connection between the two sets of clusters.
n <- nrow(pca)
x <- rep("A",n)
pc3 <- pca[,"PC3"]
pc4 <- pca[,"PC4"]
x[pc4 > 0.13 | 0.17 - pc3/1.9 < pc4] <- "B"
x[pc4 > 0.75] <- "C"
samples_68k$cluster <- x
p7 <- pca_plot_with_labels(fit_68k,c("PC3","PC4"),x) +
labs(fill = "cluster")
print(p7)
The vast majority of the cells are in cluster A:
table(samples_68k$cluster)
#
# A B C
# 63408 5006 165Looking more closely at cluster B…
L <- poisson2multinom(fit_68k)$L
pdat <- cbind(L,samples_68k["celltype"])
rows <- which(samples_68k$cluster == "c2")
levels(pdat$celltype) <- pbmc_68k_celltype_colors
TernaryPlot(alab = "k3",blab = "k5",clab = "k6",
grid.col = "gainsboro",grid.minor.lines = 0)
TernaryPoints(pdat[rows,c(3,5,6)],pch = 21,cex = 0.65,col = "white",
bg = as.character(pdat[rows,"celltype"]))TO DO: Add text here.
set.seed(1)
pbmc_68k_topics <- c(2,5,1,3,4,6)
pbmc_68k_topic_colors <- c("darkorange","olivedrab","dodgerblue",
"gray","royalblue","magenta")
rows <- sort(c(sample(which(samples_68k$cluster == "c1"),1400),
sample(which(samples_68k$cluster == "c2"),500),
which(samples_68k$cluster == "c3")))
p4 <- structure_plot(select(poisson2multinom(fit_68k),loadings = rows),
grouping = samples_68k[rows,"cluster"],
topics = pbmc_68k_topics,
colors = pbmc_68k_topic_colors[pbmc_68k_topics],
gap = 40,num_threads = 4,verbose = FALSE)
print(p4)TO DO: Before comparing to Zheng et al (2017) labeling, do more manual identification of clusters from the PCA plots.
Comparison to Zheng et al (2017) cell-type labeling of the FACS-purified PBMC data. In fit_purified, cluster 2 captures B-cells; cluster 3 is almost exclusively CD34+ and CD14+ monocytes:
Now let’s look more closely at cluster 1 in fit_purified:
par(mar = c(0,0,0,0))
rows <- which(samples_purified$cluster == "c1")
TernaryPlot(alab = "k1",blab = "k4",clab = "k6",
grid.col = "gainsboro",grid.minor.lines = 0)
TernaryPoints(pdat[rows,c(1,4,6)],pch = 21,cex = 0.65,col = "white",
bg = as.character(pdat[rows,"celltype"]))In fit_68k, cluster 2 mostly consists of CD14+ monocyte and dendritic cells, whereas cluster 3 is a small population of CD34+ cells.
with(samples_68k,table(celltype,cluster))Finally, let’s look more closely at cluster 1 in fit_68k:
par(mar = c(0,0,0,0))
rows <- which(samples_68k$cluster == "c1")
TernaryPlot(alab = "k2",blab = "k4",clab = "k6",
grid.col = "gainsboro",grid.minor.lines = 0)
TernaryPoints(pdat[rows,c(2,4,6)],pch = 21,cex = 0.65,col = "white",
bg = as.character(pdat[rows,"celltype"]))p4 <- pca_plot_with_labels(fit_purified,c("PC1","PC2"),
samples_purified$celltype,
purified_celltype_colors) + labs(fill = "celltype")
p5 <- pca_plot_with_labels(fit_purified,c("PC4","PC5"),
samples_purified$celltype,
purified_celltype_colors) + labs(fill = "celltype")pbmc_purified_celltype_colors <-
c("dodgerblue", # CD19+ B
"forestgreen", # CD14+ Monocyte
"palegreen", # CD34+
"plum", # CD4+ T Helper2
"gray", # CD56+ NK
"tomato", # CD8+ Cytotoxic T
"gold", # CD4+/CD45RO+ Memory
"magenta", # CD8+/CD45RA+ Naive Cytotoxic
"darkorange", # CD4+/CD45RA+/CD25- Naive T
"yellowgreen") # CD4+/CD25 T RegLoadings plot:
loadings_plot(poisson2multinom(fit_purified),samples_purified$celltype)
loadings_plot(poisson2multinom(fit_68k),samples_68k$celltype)PCA plot:
clrs <- c("forestgreen", # CD14+ Monocyte
"dodgerblue", # CD19+ B
"darkmagenta", # CD34+"
"yellowgreen", # CD4+ T Helper2
"gold", # CD4+/CD25 T Reg
"limegreen", # CD4+/CD45RA+/CD25- Naive T
"orange", # CD4+/CD45RO+ Memory"
"gray", # CD56+ NK
"tomato", # CD8+ Cytotoxic T
"magenta", # CD8+/CD45RA+ Naive Cytotoxic"
"darkblue") # Dendritic"
fit2 <- poisson2multinom(fit)
pca <- prcomp(fit2$L)
pdat <- cbind(samples,pca$x)
ggplot(pdat,aes(x = PC3,y = PC4,fill = celltype)) +
geom_point(shape = 21,color = "white",size = 1.5) +
scale_fill_manual(values = clrs) +
theme_cowplot(font_size = 10)t-SNE plot:
set.seed(1)
p2 <- tsne_plot(fit,n = 8000,num_threads = 4)Differential count analysis:
diff_count_res <- diff_count_analysis(fit,counts)Volcano plots:
p3 <- volcano_plot(diff_count_res,labels = genes$symbol,
label_above_quantile = 0.995)Structure plots:
set.seed(1)
fit2 <- select(poisson2multinom(fit),
loadings = which(samples$celltype == "CD19+ B"))
p4 <- structure_plot(fit2,n = 2000,num_threads = 4) # B-cells.
set.seed(1)
fit2 <- select(poisson2multinom(fit),
loadings = which(samples$celltype == "CD56+ NK"))
p5 <- structure_plot(fit2,n = 2000,num_threads = 4) # NK cells.
set.seed(1)
fit2 <- select(poisson2multinom(fit),
loadings = which(samples$celltype == "CD34+"))
p6 <- structure_plot(fit2,num_threads = 4,perplexity = 50) # CD34+ cells
set.seed(1)
fit2 <- select(poisson2multinom(fit),
loadings = which(samples$celltype == "CD14+ Monocyte"))
p7 <- structure_plot(fit2,num_threads = 4) # CD14+ monocytes
set.seed(1)
fit2 <- select(poisson2multinom(fit),
loadings = which(samples$celltype == "Dendritic"))
p8 <- structure_plot(fit2,num_threads = 4) # dendritic cells
plot_grid(p7,p8,nrow = 2)
set.seed(1)
fit2 <- select(poisson2multinom(fit),
loadings = which(samples$celltype == "CD4+ T Helper2"))
p9 <- structure_plot(fit2,num_threads = 4,perplexity = 30) +
ggtitle("CD4+ T Helper2") +
set.seed(1)
fit2 <- select(poisson2multinom(fit),
loadings = which(samples$celltype == "CD4+/CD45RA+/CD25- Naive T"))
p10 <- structure_plot(fit2,num_threads = 4) +
ggtitle("CD4+/CD45RA+/CD25- Naive T")
set.seed(1)
fit2 <- select(poisson2multinom(fit),
loadings = which(samples$celltype == "CD4+/CD45RO+ Memory"))
p11 <- structure_plot(fit2,num_threads = 4) +
ggtitle("CD4+/CD45RO+ Memory")
set.seed(1)
fit2 <- select(poisson2multinom(fit),
loadings = which(samples$celltype == "CD4+/CD25 T Reg"))
p12 <- structure_plot(fit2,num_threads = 4) +
ggtitle("CD4+/CD25 T Reg")
fit2 <- select(poisson2multinom(fit),
loadings = which(samples$celltype == "CD8+/CD45RA+ Naive Cytotoxic"))
p13 <- structure_plot(fit2,num_threads = 4) +
ggtitle("CD8+/CD45RA+ Naive Cytotoxic")
fit2 <- select(poisson2multinom(fit),
loadings = which(samples$celltype == "CD8+ Cytotoxic T"))
p14 <- structure_plot(fit2,num_threads = 4) +
ggtitle("CD8+ Cytotoxic T")
plot_grid(p9,p10,p11,p12,p13,p14,nrow = 6)Another structure plot:
p15 <- structure_plot(fit,num_threads = 4)
sessionInfo()
# R version 3.6.2 (2019-12-12)
# Platform: x86_64-apple-darwin15.6.0 (64-bit)
# Running under: macOS Catalina 10.15.5
#
# Matrix products: default
# BLAS: /Library/Frameworks/R.framework/Versions/3.6/Resources/lib/libRblas.0.dylib
# LAPACK: /Library/Frameworks/R.framework/Versions/3.6/Resources/lib/libRlapack.dylib
#
# locale:
# [1] en_US.UTF-8/en_US.UTF-8/en_US.UTF-8/C/en_US.UTF-8/en_US.UTF-8
#
# attached base packages:
# [1] stats graphics grDevices utils datasets methods base
#
# other attached packages:
# [1] Ternary_1.1.4 cowplot_1.0.0 ggplot2_3.3.0 fastTopics_0.3-163
# [5] dplyr_0.8.3
#
# loaded via a namespace (and not attached):
# [1] ggrepel_0.9.0 Rcpp_1.0.3 lattice_0.20-38
# [4] tidyr_1.0.0 prettyunits_1.1.1 assertthat_0.2.1
# [7] zeallot_0.1.0 rprojroot_1.3-2 digest_0.6.23
# [10] R6_2.4.1 backports_1.1.5 MatrixModels_0.4-1
# [13] evaluate_0.14 coda_0.19-3 httr_1.4.1
# [16] pillar_1.4.3 rlang_0.4.5 progress_1.2.2
# [19] lazyeval_0.2.2 data.table_1.12.8 irlba_2.3.3
# [22] SparseM_1.78 whisker_0.4 Matrix_1.2-18
# [25] rmarkdown_2.3 labeling_0.3 Rtsne_0.15
# [28] stringr_1.4.0 htmlwidgets_1.5.1 munsell_0.5.0
# [31] compiler_3.6.2 httpuv_1.5.2 xfun_0.11
# [34] pkgconfig_2.0.3 mcmc_0.9-6 htmltools_0.4.0
# [37] tidyselect_0.2.5 tibble_2.1.3 workflowr_1.6.2.9000
# [40] quadprog_1.5-8 viridisLite_0.3.0 crayon_1.3.4
# [43] withr_2.1.2 later_1.0.0 MASS_7.3-51.4
# [46] grid_3.6.2 jsonlite_1.6 gtable_0.3.0
# [49] lifecycle_0.1.0 git2r_0.26.1 magrittr_1.5
# [52] scales_1.1.0 RcppParallel_4.4.4 stringi_1.4.3
# [55] farver_2.0.1 fs_1.3.1 promises_1.1.0
# [58] vctrs_0.2.1 tools_3.6.2 glue_1.3.1
# [61] purrr_0.3.3 hms_0.5.2 yaml_2.2.0
# [64] colorspace_1.4-1 plotly_4.9.2 knitr_1.26
# [67] quantreg_5.54 MCMCpack_1.4-5