IRIS-FGM: an integrative single-cell RNA-Seq interpretation system for functional gene module analysis
Year: 2021
Type: article
Abstract: SUMMARY: Single-cell RNA-Seq (scRNA-Seq) data is useful in discovering cell heterogeneity and signature genes in specific cell populations in cancer and other complex diseases. Specifically, the investigation of condition-specific functional gene modules (FGM) can help to understand interactive gene networks and complex biological processes in different cell clusters. QUBIC2 is recognized as one of the most efficient and effective biclustering tools for condition-specific FGM identification from scRNA-Seq data. However, its limited availability to a C implementation restricted its application to only a few downstream analysis functionalities. We developed an R package named IRIS-FGM (Integrative scRNA-Seq Interpretation System for Functional Gene Module analysis) to support the investigation of FGMs and cell clustering using scRNA-Seq data. Empowered by QUBIC2, IRIS-FGM can effectively identify condition-specific FGMs, predict cell types/clusters, uncover differentially expressed genes and perform pathway enrichment analysis. It is noteworthy that IRIS-FGM can also take Seurat objects as input, facilitating easy integration with the existing analysis pipeline. AVAILABILITY AND IMPLEMENTATION: IRIS-FGM is implemented in the R environment (as of version 3.6) with the source code freely available at https://github.com/BMEngineeR/IRISFGM. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Source: Bioinformatics
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: green
Awards: G2041606102, G2971460396, Thrombocytes in Cancer Immunity, G3310236632, Statistical Models for Genetic Studies, Using Network and Integrative Analysis, G5536946990, Algorithms for Literature-Guided Multi-Platform Identification of Cancer Subtypes, G6422036449, Construction of cell specific gene co-regulations signatures based on single cell transcriptomics analysis, Endoplasmic Reticulum Chaperones in Cancer Biology and Therapy, The Genetic Basis of Opioid Dependence Vulnerablility in a Rodent Model, Cancer Center Support Grant
OpenAlex ID: W3096626728
