Chapter 3 🌱 Tumor Microenviroment Analysis
3.2 Derive the Proportions of Different TME Cell Types
You can use the function deconv_TME() to derive the proportions of different tumor microenvironment cell types from gene expression data with these tools.
3.3 Visualization and Comparing the Cell Proportions
cell1 <- c("T cells CD4","Neutrophil", "Macrophage","mDCs","B cells", "T cells CD8")
pie1 <- fraction_pie(cell_name_filter(frac1),feature=factor(cell1, levels = cell1))
cell2 <- c("DCs resting", "T cells CD8", "T cells CD4 naive", "Macrophages M2", "Yd T cells", "Monocytes","Mast cells resting", "Neutrophils", "Tregs","B cells naive")
pie2 <- fraction_pie(cell_name_filter(frac2[[1]][1:22,]),feature=factor(cell2, levels = cell2))
3.4 Searching for Key Cell Types Influencing Immune Therapy Response
## TIMER
TM <- deconv_TME(MEL_GSE91061,method = "TIMER")
TM_SE <- SummarizedExperiment(assays=SimpleList(TM),
colData=colData(MEL_GSE91061))
browse_biomk(SE=TM_SE)
📝 More Details about TME Analysis
TIMER is a comprehensive tool for systematical analysis of immune infiltrates across diverse cancer types.
CIBERSORT is an analytical tool from the Alizadeh Lab and Newman Lab to impute gene expression profiles and provide an estimation of the abundances of member cell types in a mixed cell population, using gene expression data.
xCell is a gene signatures-based method learned from thousands of pure cell types from various sources. xCell applies a novel technique for reducing associations between closely related cell types.
ConsensusTME a consensus approach to generating cancer specific signatures for multiple cell types found within the tumour microenvironment.