1. Differential expression analysis

load packages

library(DESeq2)
library(tidyverse)
library(ggsci)
library(matrixStats)
library(piano)
library(reshape2)
library(genefilter)
library(Biobase)
library(ComplexHeatmap)
library(ggplot2)
library(gtable)
library(grid)
library(circlize)
library(gridExtra)
library(ggpubr)
library(RColorBrewer)
library(clusterProfiler)
library(msigdbr)
library(org.Hs.eg.db)
library(enrichplot)
library(here)

load data

data_dir <- here("data")
output_dir <- here("output")
figure_dir <- here("output/figures")

#dds data set. gene expression data + patmetadata
load(paste0(data_dir, "/ddsrnaCLL_150218.RData"))

variant <- "SF3B1"
#filter for patients without NA in variant
ddsCLL <- ddsCLL[, !is.na(colData(ddsCLL)[,variant])]

#differentially expressed genes between SF3B1 groups (see differential expression.html)
diff_all <- read.csv(file=paste0(output_dir, "/diff_genes/", variant, "_diffGenes.csv"))


rownames(diff_all) <- diff_all$X
diff_all <- diff_all[which(diff_all$padj < 0.01 ),-1]
diff <- diff_all[which( abs(diff_all$stat) > 5),]


mutStatus <- data.frame(colData(ddsCLL)) %>% arrange(SF3B1)
colnames(ddsCLL) <-colData(ddsCLL)$PatID
ddsCLL <- ddsCLL[, mutStatus$PatID]

#expression data
ddsCLL <- estimateSizeFactors(ddsCLL)
RNAnorm <- varianceStabilizingTransformation(ddsCLL, blind = T)

Expression matrix

#filter for sign. genes in variant
exprMat <- assay(RNAnorm)
exprVariant <- exprMat[rownames(diff),]
colnames(exprVariant) <- colData(ddsCLL)$PatID
exprVariant.new <- log2(exprVariant)
exprVariant.new <- t(scale(t(exprVariant.new)))
exprVariant.new[exprVariant.new > 4] <- 4
exprVariant.new[exprVariant.new < -4] <- -4
rownames(exprVariant.new) <- rowData(RNAnorm[rownames(diff),])$symbol

Expression signature

#colors
colors = colorRamp2(c(-4,-1,0,1,4), c("#2166ac","#4393c3", "#f7f7f7", "#d6604d","#b2182b"))
annocol <- get_palette("jco", 10)
annocolor <- list(SF3B1 = c("1" = annocol[8], "0" = annocol[9]))
rowcolors <-colorRampPalette(brewer.pal(5, "Set1"))(5)
rowcolors[6] <- "white"


feature <- as.data.frame(colData(ddsCLL)[,c(variant)])
colnames(feature) <- c(variant)  

ha_col <- HeatmapAnnotation(df = feature, col = annocolor, annotation_height = unit(c(rep(1.9, 1)), "cm"), 
                            simple_anno_size = unit(1, "cm"),
                            annotation_name_gp = gpar(fontsize = 22, fontface = "bold"),
                            annotation_legend_param = list(title_gp = gpar(fontsize = 23), 
                                                           labels_gp = gpar(fontsize = 18),  
                                                           grid_height = unit(1.2, "cm"), 
                                                           grid_width = unit(1.2, "cm")))


#Annotate top 50 genes
diff <- diff_all[which(abs(diff_all$stat) > 6),]
sub_names <- unique(diff$Symbol)
geneIDs <- which(rownames(exprVariant.new) %in% sub_names)
rownames(exprVariant.new)[-geneIDs] <- ""

h1 <- Heatmap(exprVariant.new ,                                                     
              km = 2,
              gap = unit(0.5, "cm"),
              cluster_columns = F,
              clustering_distance_rows = "pearson",
              clustering_method_rows = "ward.D2",
              column_title = paste0("Gene signature: ", variant),                      
              col = colors,
              column_title_gp = gpar(fontsize = 25, fontface = "bold"), 
              heatmap_legend_param = list(title = "expr", 
                                          title_gp = gpar(fontsize = 23), 
                                          grid_height = unit(1.5, "cm"), 
                                          grid_width = unit(1.2, "cm"), 
                                          gap = unit(2, "cm"), 
                                          labels_gp = gpar(fontsize = 18)), 
              column_dend_height = unit(1, "cm"),
              show_row_dend = FALSE, 
              show_column_names = FALSE , 
              show_row_names = TRUE, 
              row_names_gp = gpar(fontsize = 17),
              top_annotation = ha_col)


#svg(filename=paste0(figure_dir, "/", variant, "_gene_expr.svg"), width=30, height=45)
#pdf(file=paste0(figure_dir, "/", variant, "_gene_expr.pdf"), width=22, height=25)

draw(h1) 

Past versions of “complex heatmap-1.png”

#dev.off()
saveRDS(h1, file = paste0(output_dir, "/figures/r_objects/SF3B1/SF3B1_heatmap.rds"))

Gene set enrichment analysis

Gene sets

#load gene set collection
#Hallmark
gsc <- loadGSC("/home/almut/Dokumente/masterarbeit/data/h.all.v6.0.symbols.gmt", type="gmt")
#Kegg
gsc_Kegg <- loadGSC("/home/almut/Dokumente/masterarbeit/data/c2.cp.kegg.v6.0.symbols.gmt", type="gmt")


#get all de outputs
load(paste0(output_dir,"/desRes_250720.RData"))
difftab <- function(condition){
  dataTab <- data.frame(res_list[[condition]])
  dataTab$ID <- rownames(dataTab)
  #filter using pvalues
  dataTab <- dataTab %>%
    arrange(padj) %>%
    mutate(Symbol = rowData(ddsCLL[ID,])$symbol)# %>%
    #filter(abs(log2FoldChange) > 2)
  dataTab <- dataTab[!duplicated(dataTab$Symbol),]
  dataTab <- dataTab[!is.na(dataTab$Symbol),]
  rownames(dataTab) <- dataTab$ID
   dataTab
}

diff_res <- difftab(variant)

#clusterProfiler
diff_res <- diff_res[-which(diff_res$Symbol %in% c("", NA)),]
gene_list <- diff_res$stat %>% set_names(diff_res$Symbol)
gene_list <- sort(gene_list, decreasing = TRUE)
gene_lfc <- diff_res$log2FoldChange %>% set_names(diff_res$Symbol)
gene_lfc <- sort(gene_lfc, decreasing = TRUE)
de_gene <- diff_res %>% filter(padj < 0.01) 
de_gene <- de_gene$Symbol

de_ens <- diff_res %>% filter(padj < 0.01)
de_ens <- de_ens$ID
#Get Gene IDs
gene_id <- bitr(de_ens, fromType = "ENSEMBL",
        toType = c("ENTREZID", "SYMBOL"),
        OrgDb = org.Hs.eg.db)

'select()' returned 1:many mapping between keys and columns

Warning in bitr(de_ens, fromType = "ENSEMBL", toType = c("ENTREZID",
"SYMBOL"), : 11.89% of input gene IDs are fail to map...

gene_list_id <- bitr(diff_res$ID, fromType = "ENSEMBL",
        toType = c("ENTREZID", "SYMBOL"),
        OrgDb = org.Hs.eg.db)

'select()' returned 1:many mapping between keys and columns

Warning in bitr(diff_res$ID, fromType = "ENSEMBL", toType = c("ENTREZID", :
18.07% of input gene IDs are fail to map...

names(gene_list_id) <- c("ID", "ENTREZID", "Symbol")
diff_id <- left_join(gene_list_id, diff_res)

Joining, by = c("ID", "Symbol")

gene_list_id <- diff_id$stat %>% set_names(diff_id$ENTREZID)
gene_list_id <- sort(gene_list_id, decreasing = TRUE)
gene_lfc_id <- diff_id$log2FoldChange %>% set_names(diff_id$ENTREZID)
gene_lfc_id <- sort(gene_lfc_id, decreasing = TRUE)

#convert gsc
m_t2g <- msigdbr(species = "Homo sapiens", category = "H") %>% 
  dplyr::select(gs_name, human_gene_symbol)

#Hallmark
em2 <- GSEA(gene_list, TERM2GENE = m_t2g, pvalueCutoff = 0.1)

preparing geneSet collections...

GSEA analysis...

Warning in fgsea(pathways = geneSets, stats = geneList, nperm = nPerm, minSize = minGSSize, : There are ties in the preranked stats (0% of the list).
The order of those tied genes will be arbitrary, which may produce unexpected results.

leading edge analysis...

done...

em <- enricher(de_gene, TERM2GENE = m_t2g)

#Kegg
kk <- enrichKEGG(gene_id$ENTREZID,
                 organism     = 'hsa',
                 pvalueCutoff = 0.2)

kk2 <- gseKEGG(geneList     = gene_list_id,
               organism     = 'hsa',
               nPerm        = 1000,
               minGSSize    = 50,
               pvalueCutoff = 0.2,
               verbose      = FALSE)

kk2x <- setReadable(kk2, 'org.Hs.eg.db', 'ENTREZID')

Visualize ClusterProfiler results

barplot(kk, showCategory=5)

barplot(em, showCategory=5)

dot1 <- clusterProfiler::dotplot(em2, showCategory=10) + ggtitle("GSEA for SF3B1") +
  theme_pubr() +
  theme(legend.position="right") + 
  theme(plot.title = element_text(face = "bold")) 

wrong orderBy parameter; set to default `orderBy = "x"`

dot1

dotplot(em, showCategory=10) + ggtitle("Enrichment for SF3B1")

wrong orderBy parameter; set to default `orderBy = "x"`

dotplot(kk2, showCategory=10) + ggtitle("GSEA for SF3B1")

wrong orderBy parameter; set to default `orderBy = "x"`

dot2 <- clusterProfiler::dotplot(kk, showCategory=10) + ggtitle("Enrichment for SF3B1") +
  theme_pubr() +
  theme(legend.position="right") +
  theme(plot.title = element_text(face = "bold"))

wrong orderBy parameter; set to default `orderBy = "x"`

dot2

ridgeplot(em2)

Picking joint bandwidth of 0.366

ridgeplot(kk2)

Picking joint bandwidth of 0.306

gseaplot2(em2, geneSetID = 3, title = em2$Description[3])

gseaplot2(kk2, geneSetID = 2, title = kk2$Description[2])

saveRDS(dot1, file = paste0(output_dir, "/figures/r_objects/SF3B1/enrich_dot_hm.rds"))
saveRDS(dot2, file = paste0(output_dir, "/figures/r_objects/SF3B1/enrich_dot2.rds"))

network plot

# Networks Hallmark
 em2_sub <- em2
 em2_sub@result <- em2@result[which(em2@result$Description %in% c("HALLMARK_TNFA_SIGNALING_VIA_NFKB",
                                                                    "HALLMARK_INTERFERON_ALPHA_RESPONSE",
                                                                    "HALLMARK_APOPTOSIS")),]
p_net <- cnetplot(em2_sub, categorySize="pvalue", foldChange=gene_lfc) + 
  scale_colour_gradientn(colors = c("#581845", "#900C3F", "#C70039", "#FF5733", "#FFC300", "#DAF7A6")) + 
  guides(size = FALSE) + 
  labs(color = "logFC")

Scale for 'colour' is already present. Adding another scale for
'colour', which will replace the existing scale.

p_net  

# Networks KEGG
 kk2_sub <- kk2x
 kk2_sub@result <- kk2x@result[which(kk2x@result$Description %in% c("Cytokine-cytokine receptor interaction",
                                                                    "Phosphatidylinositol signaling system"
                                                                    )),]

pnet_kegg <- cnetplot(kk2_sub, categorySize="pvalue", foldChange=gene_lfc) + 
  scale_color_gradient(high="blue", low="red") +
  guides(size = FALSE) + 
  labs(color = "logFC")

Scale for 'colour' is already present. Adding another scale for
'colour', which will replace the existing scale.

pnet_kegg

saveRDS(pnet_kegg, file = paste0(output_dir, "/figures/r_objects/SF3B1/enrich_net_kegg.rds"))
saveRDS(p_net, file = paste0(output_dir, "/figures/r_objects/SF3B1/enrich_net_hm.rds"))

heatplot

heatplot(em2, foldChange=gene_lfc, showCategory = 3)

heatplot(kk2x, foldChange=gene_lfc, showCategory = 3 ) 

Session information

sessionInfo()

R version 3.6.3 (2020-02-29)
Platform: x86_64-pc-linux-gnu (64-bit)
Running under: Ubuntu 16.04.7 LTS

Matrix products: default
BLAS:   /usr/lib/libblas/libblas.so.3.6.0
LAPACK: /usr/lib/lapack/liblapack.so.3.6.0

locale:
 [1] LC_CTYPE=de_DE.UTF-8       LC_NUMERIC=C              
 [3] LC_TIME=de_DE.UTF-8        LC_COLLATE=de_DE.UTF-8    
 [5] LC_MONETARY=de_DE.UTF-8    LC_MESSAGES=de_DE.UTF-8   
 [7] LC_PAPER=de_DE.UTF-8       LC_NAME=C                 
 [9] LC_ADDRESS=C               LC_TELEPHONE=C            
[11] LC_MEASUREMENT=de_DE.UTF-8 LC_IDENTIFICATION=C       

attached base packages:
 [1] grid      parallel  stats4    stats     graphics  grDevices utils    
 [8] datasets  methods   base     

other attached packages:
 [1] here_0.1                    enrichplot_1.4.0           
 [3] org.Hs.eg.db_3.8.2          AnnotationDbi_1.46.0       
 [5] msigdbr_7.0.1               clusterProfiler_3.12.0     
 [7] RColorBrewer_1.1-2          ggpubr_0.2                 
 [9] magrittr_1.5                gridExtra_2.3              
[11] circlize_0.4.6              gtable_0.3.0               
[13] ComplexHeatmap_2.0.0        genefilter_1.66.0          
[15] reshape2_1.4.3              piano_2.0.2                
[17] ggsci_2.9                   forcats_0.4.0              
[19] stringr_1.4.0               dplyr_0.8.1                
[21] purrr_0.3.2                 readr_1.3.1                
[23] tidyr_0.8.3                 tibble_2.1.3               
[25] ggplot2_3.1.1               tidyverse_1.2.1            
[27] DESeq2_1.24.0               SummarizedExperiment_1.14.0
[29] DelayedArray_0.10.0         BiocParallel_1.18.0        
[31] matrixStats_0.54.0          Biobase_2.44.0             
[33] GenomicRanges_1.36.0        GenomeInfoDb_1.20.0        
[35] IRanges_2.18.1              S4Vectors_0.22.0           
[37] BiocGenerics_0.30.0        

loaded via a namespace (and not attached):
  [1] shinydashboard_0.7.1   tidyselect_0.2.5       RSQLite_2.1.1         
  [4] htmlwidgets_1.3        munsell_0.5.0          DT_0.7                
  [7] withr_2.1.2            colorspace_1.4-1       GOSemSim_2.10.0       
 [10] knitr_1.23             rstudioapi_0.10        DOSE_3.10.2           
 [13] labeling_0.3           git2r_0.25.2           slam_0.1-45           
 [16] urltools_1.7.3         GenomeInfoDbData_1.2.1 polyclip_1.10-0       
 [19] bit64_0.9-7            farver_2.0.3           rprojroot_1.3-2       
 [22] generics_0.0.2         xfun_0.7               sets_1.0-18           
 [25] R6_2.4.0               clue_0.3-57            graphlayouts_0.6.0    
 [28] locfit_1.5-9.1         bitops_1.0-6           fgsea_1.10.0          
 [31] gridGraphics_0.5-0     assertthat_0.2.1       promises_1.0.1        
 [34] scales_1.0.0           ggraph_2.0.2           nnet_7.3-14           
 [37] tidygraph_1.1.2        workflowr_1.4.0        rlang_0.3.4           
 [40] GlobalOptions_0.1.0    splines_3.6.3          lazyeval_0.2.2        
 [43] acepack_1.4.1          broom_0.5.2            europepmc_0.3         
 [46] checkmate_1.9.3        BiocManager_1.30.4     yaml_2.2.0            
 [49] modelr_0.1.4           backports_1.1.4        httpuv_1.5.1          
 [52] qvalue_2.16.0          Hmisc_4.2-0            tools_3.6.3           
 [55] relations_0.6-8        ggplotify_0.0.5        gplots_3.0.1.1        
 [58] ggridges_0.5.2         Rcpp_1.0.1             plyr_1.8.4            
 [61] base64enc_0.1-3        visNetwork_2.0.7       progress_1.2.2        
 [64] zlibbioc_1.30.0        RCurl_1.95-4.12        prettyunits_1.0.2     
 [67] rpart_4.1-15           GetoptLong_0.1.7       viridis_0.5.1         
 [70] cowplot_0.9.4          haven_2.1.0            ggrepel_0.8.1         
 [73] cluster_2.1.0          fs_1.3.1               data.table_1.12.2     
 [76] DO.db_2.9              triebeard_0.3.0        whisker_0.3-2         
 [79] hms_0.4.2              shinyjs_1.0            mime_0.7              
 [82] evaluate_0.14          xtable_1.8-4           XML_3.98-1.20         
 [85] readxl_1.3.1           shape_1.4.4            compiler_3.6.3        
 [88] KernSmooth_2.23-15     crayon_1.3.4           htmltools_0.3.6       
 [91] later_0.8.0            Formula_1.2-3          geneplotter_1.62.0    
 [94] lubridate_1.7.4        DBI_1.0.0              tweenr_1.0.1          
 [97] MASS_7.3-53            Matrix_1.3-0           cli_1.1.0             
[100] marray_1.62.0          gdata_2.18.0           igraph_1.2.4.1        
[103] pkgconfig_2.0.2        rvcheck_0.1.8          foreign_0.8-76        
[106] xml2_1.2.0             annotate_1.62.0        XVector_0.24.0        
[109] rvest_0.3.4            digest_0.6.19          rmarkdown_1.13        
[112] cellranger_1.1.0       fastmatch_1.1-0        htmlTable_1.13.1      
[115] shiny_1.3.2            gtools_3.8.1           rjson_0.2.20          
[118] nlme_3.1-151           jsonlite_1.6           viridisLite_0.3.0     
[121] limma_3.40.2           pillar_1.4.1           lattice_0.20-38       
[124] httr_1.4.0             survival_2.44-1.1      GO.db_3.8.2           
[127] glue_1.3.1             UpSetR_1.4.0           png_0.1-7             
[130] bit_1.1-14             ggforce_0.3.1          stringi_1.4.3         
[133] blob_1.1.1             latticeExtra_0.6-28    caTools_1.17.1.2      
[136] memoise_1.1.0