Last updated: 2019-10-29
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library(Seurat)
library(WGCNA)
library(cluster)
library(parallelDist)
library(ggsci)
library(emmeans)
library(lme4)
library(ggbeeswarm)
library(genefilter)
library(tidyverse)
library(reshape2)
library(igraph)
library(gProfileR)
library(ggpubr)
library(princurve)
library(here)
library(cowplot)
pcembed <- as.matrix(Embeddings(ventric, reduction = "pca")[,c(1:2)])
y <- principal_curve(pcembed)
color <- as.factor(ventric$predicted.id)
levels(color) <- c("#E41A1C", "#377EB8", "#4DAF4A", "#984EA3")
df = data.frame(y$s[order(y$lambda), ])
colnames(df) = c("x", "y")
points <- data.frame(id = ventric$predicted.id, Embeddings(ventric, reduction = "pca")[,c(1:2)])
rand <- sample(nrow(points), 3000)
princ_plot <- ggplot(data = df, aes(x, y)) +
geom_point(data = points[rand,], aes(x=PC_1, y=PC_2, colour=factor(id)), size = 2, inherit.aes = F, alpha=0.5) +
geom_line(size = 2, color = "black") +
theme_pubr(legend = "none") +
xlim(c(-20,10)) + coord_flip() + xlab("PC_1") + ylab("PC_2") + theme( axis.text.x = element_text(angle=45, hjust=1))
ventric$height <- y$lambda
princ_plot
Warning: Removed 37 rows containing missing values (geom_point).
Warning: Removed 122 rows containing missing values (geom_path).
Version | Author | Date |
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3b5cbe7 | Full Name | 2019-10-28 |
enableWGCNAThreads()
Allowing parallel execution with up to 79 working processes.
datExpr<-as.matrix(t(ventric[["SCT"]]@scale.data[ventric[["SCT"]]@var.features,]))
gsg = goodSamplesGenes(datExpr, verbose = 3)
Flagging genes and samples with too many missing values...
..step 1
powers = c(c(1:10), seq(from = 12, to=40, by=2))
sft=pickSoftThreshold(datExpr,dataIsExpr = TRUE, powerVector = powers, corOptions = list(use = 'p'),
networkType = "signed")
Power SFT.R.sq slope truncated.R.sq mean.k. median.k. max.k.
1 1 0.25800 164.00 0.536 2.50e+03 2.50e+03 2.53e+03
2 2 0.19200 73.30 0.572 1.25e+03 1.25e+03 1.28e+03
3 3 0.12600 38.60 0.604 6.26e+02 6.26e+02 6.46e+02
4 4 0.09260 24.20 0.644 3.13e+02 3.13e+02 3.28e+02
5 5 0.04690 14.10 0.664 1.57e+02 1.57e+02 1.66e+02
6 6 0.02260 8.43 0.662 7.86e+01 7.85e+01 8.45e+01
7 7 0.00326 2.68 0.666 3.93e+01 3.93e+01 4.30e+01
8 8 0.01880 -5.74 0.627 1.97e+01 1.97e+01 2.19e+01
9 9 0.06610 -9.63 0.614 9.87e+00 9.85e+00 1.12e+01
10 10 0.20800 -14.80 0.560 4.94e+00 4.93e+00 5.74e+00
11 12 0.67700 -22.60 0.614 1.24e+00 1.24e+00 1.56e+00
12 14 0.54100 -27.90 0.410 3.12e-01 3.10e-01 4.66e-01
13 16 0.55300 -22.30 0.439 7.85e-02 7.79e-02 1.54e-01
14 18 0.48400 -15.00 0.398 1.98e-02 1.96e-02 5.76e-02
15 20 0.42200 -9.40 0.311 5.00e-03 4.92e-03 2.47e-02
16 22 0.44500 -7.06 0.311 1.27e-03 1.24e-03 1.19e-02
17 24 0.44300 -6.08 0.360 3.24e-04 3.11e-04 6.21e-03
18 26 0.44600 -4.65 0.291 8.42e-05 7.83e-05 3.43e-03
19 28 0.48400 -4.19 0.341 2.25e-05 1.97e-05 1.96e-03
20 30 0.49100 -3.41 0.370 6.36e-06 4.97e-06 1.15e-03
21 32 0.42700 -2.89 0.264 1.97e-06 1.25e-06 6.79e-04
22 34 0.46400 -2.72 0.320 7.00e-07 3.16e-07 4.07e-04
23 36 0.47200 -2.50 0.326 2.90e-07 7.98e-08 2.46e-04
24 38 0.47800 -2.29 0.355 1.38e-07 2.02e-08 1.49e-04
25 40 0.50000 -2.25 0.357 7.18e-08 5.10e-09 9.10e-05
cex1=0.9
plot(sft$fitIndices[,1], -sign(sft$fitIndices[,3])*sft$fitIndices[,2],xlab="Soft Threshold (power)",ylab="Scale Free Topology Model Fit, signed R^2",type="n", main = paste("Scale independence"))
text(sft$fitIndices[,1], -sign(sft$fitIndices[,3])*sft$fitIndices[,2],labels=powers ,cex=cex1,col="red")
abline(h=0.80,col="red")
Version | Author | Date |
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3b5cbe7 | Full Name | 2019-10-28 |
#Mean Connectivity Plot
plot(sft$fitIndices[,1], sft$fitIndices[,5],xlab="Soft Threshold (power)",ylab="Mean Connectivity", type="n",main = paste("Mean connectivity"))
text(sft$fitIndices[,1], sft$fitIndices[,5], labels=powers, cex=cex1,col="red")
Version | Author | Date |
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3b5cbe7 | Full Name | 2019-10-28 |
softPower <- 12
SubGeneNames <- colnames(datExpr)
adj <- adjacency(datExpr, type = "signed", power = softPower)
diag(adj) <- 0
TOM <- TOMsimilarityFromExpr(datExpr, networkType = "signed", TOMType = "signed", power = softPower, maxPOutliers = 0.05)
TOM calculation: adjacency..
..will use 79 parallel threads.
Fraction of slow calculations: 0.000000
..connectivity..
..matrix multiplication (system BLAS)..
..normalization..
..done.
colnames(TOM) <- rownames(TOM) <- SubGeneNames
dissTOM <- 1 - TOM
geneTree <- hclust(as.dist(dissTOM), method = "complete") # use complete for method rather than average (gives better results)
plot(geneTree, xlab = "", sub = "", cex = .5, main = "Gene clustering", hang = .001)
Version | Author | Date |
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3b5cbe7 | Full Name | 2019-10-28 |
minModuleSize = 15
x = 2
dynamicMods = cutreeDynamic(dendro = geneTree, distM = as.matrix(dissTOM),
method="hybrid", pamStage = F, deepSplit = x,
minClusterSize = minModuleSize)
..cutHeight not given, setting it to 1 ===> 99% of the (truncated) height range in dendro.
..done.
dynamicColors = labels2colors(dynamicMods) #label each module with a unique color
plotDendroAndColors(geneTree, dynamicColors, "Dynamic Tree Cut",
dendroLabels = FALSE, hang = 0.03, addGuide = TRUE, guideHang = 0.05,
main = "Gene dendrogram and module colors") #plot the modules with colors
Version | Author | Date |
---|---|---|
3b5cbe7 | Full Name | 2019-10-28 |
MEs = moduleEigengenes(datExpr, dynamicColors)$eigengenes #this matrix gives correlations between cells and module eigengenes (a high value indicates that the cell is highly correlated with the genes in that module)
ME1<-MEs
row.names(ME1)<-row.names(datExpr)
# Calculate dissimilarity of module eigengenes
MEDiss = 1-cor(MEs);
# Cluster module eigengenes
METree = hclust(as.dist(MEDiss), method = "average");
# Plot the result
plot(METree, main = "Clustering of module eigengenes",xlab = "", sub = "")
MEDissThres = 0.2
# Plot the cut line into the dendrogram
abline(h=MEDissThres, col = "red")
Version | Author | Date |
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3b5cbe7 | Full Name | 2019-10-28 |
merge = mergeCloseModules(datExpr, dynamicColors, cutHeight = MEDissThres, verbose = 3)
mergeCloseModules: Merging modules whose distance is less than 0.2
multiSetMEs: Calculating module MEs.
Working on set 1 ...
moduleEigengenes: Calculating 35 module eigengenes in given set.
Calculating new MEs...
multiSetMEs: Calculating module MEs.
Working on set 1 ...
moduleEigengenes: Calculating 35 module eigengenes in given set.
mergedColors = merge$colors
mergedMEs = merge$newMEs
moduleColors = mergedColors
MEs = mergedMEs
modulekME = signedKME(datExpr,MEs)
plotDendroAndColors(geneTree, cbind(dynamicColors, mergedColors),
c("Dynamic Tree Cut", "Merged dynamic"),
dendroLabels = FALSE, hang = 0.03,
addGuide = TRUE, guideHang = 0.05)
Version | Author | Date |
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3b5cbe7 | Full Name | 2019-10-28 |
# Rename to moduleColors
moduleColors = mergedColors
# Construct numerical labels corresponding to the colors
# colorOrder = c("grey", standardColors(50));
# moduleLabels = match(moduleColors, colorOrder)-1
MEs = mergedMEs
modulekME = signedKME(datExpr,MEs)
#type gene name, prints out gene names also in that module
modules<-MEs
c_modules<-data.frame(moduleColors)
row.names(c_modules)<-colnames(datExpr) #assign gene names as row names
module.list.set1<-substring(colnames(modules),3) #removes ME from start of module names
index.set1<-0
Network=list() #create lists of genes for each module
for (i in 1:length(module.list.set1)){index.set1<-which(c_modules==module.list.set1[i])
Network[[i]]<-row.names(c_modules)[index.set1]}
names(Network)<-module.list.set1
lookup<-function(gene,network){return(network[names(network)[grep(gene,network)]])} #load function
nGenes = ncol(datExpr)
nSamples = nrow(datExpr)
MEs = orderMEs(MEs)
MEs %>% select(-MEgrey) -> MEs
var<-model.matrix(~0+ventric$trt)
moduleTraitCor <- cor(MEs, var, use="p")
cor<-moduleTraitCor[abs(moduleTraitCor[,1])>.2,]
moduleTraitPvalue = corPvalueStudent(moduleTraitCor, nSamples)
cor<-melt(cor)
ggplot(cor, aes(Var2, Var1)) + geom_tile(aes(fill = value),
colour = "white") + scale_fill_gradient2(midpoint = 0, low = "blue", mid = "white",
high = "red", space = "Lab", name="Correlation \nStrength") +
theme(axis.text.x = element_text(angle = 45, hjust = 1)) + xlab("Treatment") + ylab(NULL)
Version | Author | Date |
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3b5cbe7 | Full Name | 2019-10-28 |
hubgenes<-lapply(seq_len(length(Network)), function(x) {
dat<-modulekME[Network[[x]],]
dat<-dat[order(-dat[paste0("kME",names(Network)[x])]),]
gene<-rownames(dat)
return(gene)
})
names(hubgenes)<-names(Network)
d <- unlist(hubgenes)
d <- data.frame(gene = d,
vec = names(d))
write_csv(d, path=here("output/glia/wgcna/wc_tany_wgcna_genemodules.csv"))
#Function to calculate SEM and Average
summarySE <- function(data=NULL, measurevar, groupvars=NULL, na.rm=FALSE,
conf.interval=.95, .drop=TRUE) {
library(plyr)
# New version of length which can handle NA's: if na.rm==T, don't count them
length2 <- function (x, na.rm=FALSE) {
if (na.rm) sum(!is.na(x))
else length(x)
}
# This does the summary. For each group's data frame, return a vector with
# N, mean, and sd
datac <- ddply(data, groupvars, .drop=.drop,
.fun = function(xx, col) {
c(N = length2(xx[[col]], na.rm=na.rm),
mean = mean (xx[[col]], na.rm=na.rm),
sd = sd (xx[[col]], na.rm=na.rm)
)
},
measurevar
)
# Rename the "mean" column
datac$se <- datac$sd / sqrt(datac$N) # Calculate standard error of the mean
# Confidence interval multiplier for standard error
# Calculate t-statistic for confidence interval:
# e.g., if conf.interval is .95, use .975 (above/below), and use df=N-1
ciMult <- qt(conf.interval/2 + .5, datac$N-1)
datac$ci <- datac$se * ciMult
return(datac)
}
data<-data.frame(MEs, trt = ventric$trt,
sample = as.factor(ventric$sample),
batch = as.factor(ventric$batch),
height = ventric$height,
bin = cut(ventric$height, seq_len(max(ventric$height))),
type = ventric$predicted.id)
levels(data$bin) <- c(1:74)
data$bin <- as.numeric(as.character(data$bin))
data %>% filter(bin>=12 & bin <= 40) %>% mutate(bin=factor(bin)) -> data
plot <- lapply(colnames(MEs), function(x) {
x <- data.frame(scale(data[,x]))
x$bin<-data$bin
x$trt<-as.factor(data$trt)
x$type<-as.factor(data$type)
x<-melt(x, id.vars=c("trt","bin","type"))
x<-x[complete.cases(x),]
plotval <- summarySE(x, measurevar="value", groupvars = c("trt","bin"))
return(plotval)
})
names(plot) <- colnames(MEs)
plot_df <- bind_rows(plot, .id="id")
mod <- lapply(colnames(MEs)[grepl("^ME", colnames(MEs))], function(me) {
tryCatch({
mod <- lmer(data[[me]] ~ trt*bin + (1 | batch) + (1 | sample), data = data)
pairwise <- emmeans(mod, pairwise ~ trt|bin)
plot <- data.frame(plot(pairwise, plotIt = F)$data)
sig <- as.data.frame(pairwise$contrasts)
return(sig) }, error = function(err) {
print(err)
}
)
})
Warning in checkConv(attr(opt, "derivs"), opt$par, ctrl =
control$checkConv, : Model failed to converge with max|grad| = 0.0025552
(tol = 0.002, component 1)
Warning in checkConv(attr(opt, "derivs"), opt$par, ctrl =
control$checkConv, : Model failed to converge with max|grad| = 0.00659419
(tol = 0.002, component 1)
Warning in checkConv(attr(opt, "derivs"), opt$par, ctrl =
control$checkConv, : Model failed to converge with max|grad| = 0.00506122
(tol = 0.002, component 1)
Warning in checkConv(attr(opt, "derivs"), opt$par, ctrl =
control$checkConv, : Model failed to converge with max|grad| = 0.00202572
(tol = 0.002, component 1)
Warning in checkConv(attr(opt, "derivs"), opt$par, ctrl =
control$checkConv, : Model failed to converge with max|grad| = 0.00372838
(tol = 0.002, component 1)
Warning in checkConv(attr(opt, "derivs"), opt$par, ctrl =
control$checkConv, : Model failed to converge with max|grad| = 0.00204838
(tol = 0.002, component 1)
names(mod) <- colnames(MEs)
mod_df <- bind_rows(mod, .id="id")
mod_df$p.adj<-p.adjust(mod_df$p.value)
plot_df %>% filter(trt=="FGF") %>% mutate(p.adj = mod_df$p.adj) -> plot_f_df
plot_df %>% filter(trt=="PF") %>% mutate(p.adj = mod_df$p.adj) -> plot_p_df
plot_df <- rbind(plot_f_df, plot_p_df)
plot_df%>%mutate(signif=ifelse(p.adj>.05, "ns",
ifelse(p.adj<.05&p.adj>.01, "*",
ifelse(p.adj<.01&p.adj>.001, "**",
"***")))) -> plotval_frame
plotval_frame$signif[plotval_frame$signif=="ns"]<-NA
plotval_frame$signif[plotval_frame$trt!="FGF"]<-NA
detach("package:here", unload = T)
library(here)
write_csv(as.data.frame(plotval_frame), path = here("output/glia/wgcna/wc_tany_pseudovent_linmod.csv"))
mod_df %>% filter(p.adj<0.05) -> sig_df
sig_mods <- names(which(table(sig_df$id) > 5))
height_type <- ggplot() + geom_density(data=data, aes(x=(-height), fill=type), inherit.aes = F, alpha=0.25) + coord_flip() +
theme_pubr(legend = "none") + xlab("Pseudo-ventrivcle Height") + ylab(NULL) + theme(axis.text.x = element_blank(), axis.text.y = element_blank())
mod <- ggplot(plotval_frame[plotval_frame$id%in%c(sig_mods),], aes(x=(-as.numeric(as.character(bin))), y=mean, color=trt, label=signif)) +
geom_errorbar(aes(ymin=mean-se, ymax=mean+se, width=.1)) +
geom_line() + geom_point() + scale_color_manual(values=c("#000000","#999999")) +
geom_text(color="black",size=3,aes(y= mean + .5), position=position_dodge(.9), angle=90) + coord_flip() +
facet_wrap(vars(id), scales="free", nrow=1) + theme_pubr() + ylab("Scaled ME Expression") + xlab(NULL) +
theme(legend.position="none", axis.text.y = element_blank(), axis.text.x = element_text(angle=45, hjust=1))
ventric_umap <- as.data.frame(Embeddings(ventric, reduction="umap"))
ventric_umap$`Cell Type` <- ventric$predicted.id
umap <- ggplot(ventric_umap, aes(x=UMAP_1, y=UMAP_2, color=`Cell Type`)) + geom_point(alpha=0.5) + theme_void() + theme(legend.position = "top")
tany_day5 <- plot_grid(umap, princ_plot, height_type, mod, rel_widths = c(2,1,1,2.5), align = "hv", axis="tb", nrow=1, scale=0.9)
Warning: Removed 37 rows containing missing values (geom_point).
Warning: Removed 122 rows containing missing values (geom_path).
Warning: Removed 174 rows containing missing values (geom_text).
tany_day5
Version | Author | Date |
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3b5cbe7 | Full Name | 2019-10-28 |
goterms<-lapply(hubgenes[gsub(sig_mods,pattern = "ME",replacement = "")], function(x) {
x<-gprofiler(x, ordered_query = T, organism = "mmusculus", significant = T, custom_bg = colnames(datExpr),
src_filter = c("GO:BP","REAC","KEGG"), hier_filtering = "strong",
min_isect_size = 2,
sort_by_structure = T,exclude_iea = T,
min_set_size = 10, max_set_size = 300,correction_method = "fdr")
x<-x[order(x$p.value),]
return(x)
})
goterms %>% bind_rows(.id="id") %>%
mutate(padj=p.adjust(p.value, "fdr")) -> godat
write_csv(godat, path=here("output/glia/wgcna/wc_wgcna_tany_goterms.csv"))
save.image(file = here("output/glia/wgcna/wc_tany_results.RData"))
sessionInfo()
R version 3.5.3 (2019-03-11)
Platform: x86_64-pc-linux-gnu (64-bit)
Running under: Storage
Matrix products: default
BLAS/LAPACK: /usr/lib64/libopenblas-r0.3.3.so
locale:
[1] LC_CTYPE=en_DK.UTF-8 LC_NUMERIC=C
[3] LC_TIME=en_DK.UTF-8 LC_COLLATE=en_DK.UTF-8
[5] LC_MONETARY=en_DK.UTF-8 LC_MESSAGES=en_DK.UTF-8
[7] LC_PAPER=en_DK.UTF-8 LC_NAME=C
[9] LC_ADDRESS=C LC_TELEPHONE=C
[11] LC_MEASUREMENT=en_DK.UTF-8 LC_IDENTIFICATION=C
attached base packages:
[1] stats graphics grDevices utils datasets methods base
other attached packages:
[1] here_0.1 plyr_1.8.4 cowplot_1.0.0
[4] princurve_2.1.4 ggpubr_0.2.1 magrittr_1.5
[7] gProfileR_0.6.7 igraph_1.2.4.1 reshape2_1.4.3
[10] forcats_0.4.0 stringr_1.4.0 dplyr_0.8.3
[13] purrr_0.3.2 readr_1.3.1.9000 tidyr_0.8.3
[16] tibble_2.1.3 tidyverse_1.2.1 genefilter_1.64.0
[19] ggbeeswarm_0.6.0 ggplot2_3.2.1 lme4_1.1-21
[22] Matrix_1.2-17 emmeans_1.3.5.1 ggsci_2.9
[25] parallelDist_0.2.4 cluster_2.1.0 WGCNA_1.68
[28] fastcluster_1.1.25 dynamicTreeCut_1.63-1 Seurat_3.0.3.9036
loaded via a namespace (and not attached):
[1] reticulate_1.13 R.utils_2.9.0 tidyselect_0.2.5
[4] robust_0.4-18.1 RSQLite_2.1.1 AnnotationDbi_1.44.0
[7] htmlwidgets_1.3 grid_3.5.3 Rtsne_0.15
[10] munsell_0.5.0 codetools_0.2-16 ica_1.0-2
[13] preprocessCore_1.44.0 future_1.14.0 withr_2.1.2
[16] colorspace_1.4-1 Biobase_2.42.0 highr_0.8
[19] knitr_1.23 rstudioapi_0.10 stats4_3.5.3
[22] ROCR_1.0-7 robustbase_0.93-5 ggsignif_0.5.0
[25] gbRd_0.4-11 listenv_0.7.0 labeling_0.3
[28] Rdpack_0.11-0 git2r_0.25.2 bit64_0.9-7
[31] rprojroot_1.3-2 vctrs_0.2.0 coda_0.19-3
[34] generics_0.0.2 TH.data_1.0-10 xfun_0.8
[37] R6_2.4.0 doParallel_1.0.14 rsvd_1.0.2
[40] bitops_1.0-6 assertthat_0.2.1 SDMTools_1.1-221.1
[43] scales_1.0.0 multcomp_1.4-10 nnet_7.3-12
[46] beeswarm_0.2.3 gtable_0.3.0 npsurv_0.4-0
[49] globals_0.12.4 sandwich_2.5-1 workflowr_1.4.0
[52] rlang_0.4.0 zeallot_0.1.0 splines_3.5.3
[55] lazyeval_0.2.2 acepack_1.4.1 impute_1.56.0
[58] broom_0.5.2 checkmate_1.9.4 modelr_0.1.4
[61] yaml_2.2.0 backports_1.1.4 Hmisc_4.2-0
[64] tools_3.5.3 gplots_3.0.1.1 RColorBrewer_1.1-2
[67] BiocGenerics_0.28.0 ggridges_0.5.1 Rcpp_1.0.2
[70] base64enc_0.1-3 RCurl_1.95-4.12 rpart_4.1-15
[73] pbapply_1.4-1 S4Vectors_0.20.1 zoo_1.8-6
[76] haven_2.1.0 ggrepel_0.8.1 fs_1.3.1
[79] data.table_1.12.2 lmtest_0.9-37 RANN_2.6.1
[82] mvtnorm_1.0-11 whisker_0.3-2 fitdistrplus_1.0-14
[85] matrixStats_0.54.0 hms_0.5.0 lsei_1.2-0
[88] evaluate_0.14 xtable_1.8-4 XML_3.98-1.20
[91] readxl_1.3.1 IRanges_2.16.0 gridExtra_2.3
[94] compiler_3.5.3 KernSmooth_2.23-15 crayon_1.3.4
[97] minqa_1.2.4 R.oo_1.22.0 htmltools_0.3.6
[100] pcaPP_1.9-73 Formula_1.2-3 rrcov_1.4-7
[103] RcppParallel_4.4.3 lubridate_1.7.4 DBI_1.0.0
[106] MASS_7.3-51.4 boot_1.3-22 cli_1.1.0
[109] R.methodsS3_1.7.1 gdata_2.18.0 parallel_3.5.3
[112] metap_1.1 pkgconfig_2.0.2 fit.models_0.5-14
[115] foreign_0.8-71 plotly_4.9.0 xml2_1.2.0
[118] foreach_1.4.4 annotate_1.60.1 vipor_0.4.5
[121] estimability_1.3 rvest_0.3.4 bibtex_0.4.2
[124] digest_0.6.20 sctransform_0.2.0 RcppAnnoy_0.0.12
[127] tsne_0.1-3 cellranger_1.1.0 rmarkdown_1.13
[130] leiden_0.3.1 htmlTable_1.13.1 uwot_0.1.3
[133] gtools_3.8.1 nloptr_1.2.1 nlme_3.1-140
[136] jsonlite_1.6 viridisLite_0.3.0 pillar_1.4.2
[139] lattice_0.20-38 httr_1.4.1 DEoptimR_1.0-8
[142] survival_2.44-1.1 GO.db_3.7.0 glue_1.3.1
[145] png_0.1-7 iterators_1.0.10 bit_1.1-14
[148] stringi_1.4.3 blob_1.1.1 latticeExtra_0.6-28
[151] caTools_1.17.1.2 memoise_1.1.0 irlba_2.3.3
[154] future.apply_1.3.0 ape_5.3