Language
English
Publication Date
12-15-2023
Journal
STAR Protocols
DOI
10.1016/j.xpro.2023.102742
PMID
38019649
PMCID
PMC10698325
PubMedCentral® Posted Date
11-27-2023
PubMedCentral® Full Text Version
Post-Print
Abstract
Exploring the clinical relevance of diverse immune cell types within the tumor microenvironment is pivotal for unraveling cancer intricacies and developing treatments. Here, we present a protocol for using tumor immune microenvironment illustration based on gene pairs, an R package to deduce cell-cell interactions, unveiling the association between immune cell relative abundance and patient prognoses from bulk gene expression and survival data. We describe steps for harnessing cell-type markers derived from single-cell RNA sequencing data to map the tumor immune microenvironment across a spectrum of cancer types. For complete details on the use and execution of this protocol, please refer to Li et al. (2023).
Keywords
Humans, Tumor Microenvironment, Gene Expression Profiling, Cell Communication, Neoplasms, Bioinformatics, Single Cell, Cancer, Genomics, RNA-seq, Immunology, Gene Expression, Systems biology
Published Open-Access
yes
Recommended Citation
Chenyang Li, Jianjun Zhang, and Chao Cheng, "TimiGP: An R Package to Depict the Tumor Microenvironment from Bulk Transcriptomics" (2023). Faculty and Staff Publications. 1195.
https://digitalcommons.library.tmc.edu/baylor_docs/1195
Graphical Abstract
Included in
Biomedical Informatics Commons, Diseases Commons, Epidemiology Commons, Medical Genetics Commons, Medical Immunology Commons, Oncology Commons