Table 2 Strengths and weaknesses of immune cells quantification algorithms

From: Technological advances in cancer immunity: from immunogenomics to single-cell analysis and artificial intelligence

Algorithm

Category

Strengths

Weakness

ESTIMATE

G

Available for tumor purity and global immune status

Only a stromal score and an immune score are output. The information is limited27

xCell

G

Available for inference of 64 immune and stromal cell

The definitions of the cell subtypes are sometimes not clear

Accuracy of prediction of some cell types is uncertain26

MCP-counter

G

Available for inference of fibroblasts and endothelial cells

Available for an absolute quantification of specific cell population across samples

Available for between-sample comparison

Relatively less cell types included in the inference (8 types)

CIBERSORT

D

Available for inference of 22 immune cell subtypes

Available for between-cell-type comparison

Relative proportion of distinct cell types in a single sample

Trained on microarray rather than RNA-seq data30

EPIC

D

Available for inference of fibroblasts, endothelial cells, and uncharacterized cells

Enabling inference of tumor purity from uncharacterized cell proportion

Available for both between-sample and between-cell-type comparison

Only 6 immune cell types available

Not available for discrimination of cell types with transcriptional similarity

quanTIseq

D

Available for inference of 10 immune cell subtypes

Available for both between-sample and between-cell-type comparison

Not available for quantification of stromal cells (e.g., cancer-associated fibroblasts)

TIMER

D

A user-friendly analytic web tool for cancer immunology research

Only 6 immune cell types and no stromal cells available

Relative proportion of distinct cell types in a single sample

CIBERSORTx

D

Adopting a more convincing gene expression reference from single-cell sequencing

Suitability for some tumor types needs further validation

MuSiC

D

Adopting a more convincing gene expression reference from single-cell sequencing

Available for tissues with intensively correlated cell types

Suitability for some tumor types needs further validation

Not available for TPM data as input33

FARDEEP

D

A robust machine learning tool eliminating outliers in the dataset

Suitable for deconvolution of noisy datasets

Different signature matrix should be adopted according to the type of gene expression data32

  1. G GSEA-based method, D deconvolution method