IRIS-FGM

IRIS-FGM analyzes single-cell RNA sequencing (scRNA-Seq) data to identify and interpret functional gene modules (FGMs) and to derive co-expression/co-regulation patterns, cell-type clusters, differential expression, and functional enrichment.


Key Features:

  • Functional Gene Module Analysis: Identifies functional gene modules (FGMs) from scRNA-Seq data using QUBIC2.
  • Integration with Analysis Pipelines: Implemented in R (version 3.6) and accepts Seurat objects as input for integration with Seurat-based workflows.
  • Co-expression and Co-regulation Detection: Detects co-expressed and co-regulated FGMs to reveal gene interaction structures.
  • Cell Type Prediction and Clustering: Predicts cell types and performs cell clustering to characterize cellular heterogeneity.
  • Differential Expression Analysis: Identifies differentially expressed genes across clusters or cell types.
  • Functional Enrichment Analysis: Performs functional enrichment to interpret the biological significance of FGMs and gene sets.

Scientific Applications:

  • Cancer Research: Dissects tumor cellular heterogeneity and gene-module–level programs relevant to cancer biology.
  • Complex Disease Studies: Characterizes cell-type–specific gene modules and regulatory patterns in complex diseases.
  • Signature Gene and Biomarker Discovery: Supports discovery of signature genes and differentially expressed candidates for downstream validation.

Methodology:

IRIS-FGM uses QUBIC2 for FGM identification, operates in R (version 3.6) with Seurat objects as input, and implements analyses for co-expression/co-regulation detection, cell clustering and type prediction, differential expression, and functional enrichment.

Topics

Details

Tool Type:
command-line tool
Programming Languages:
C++, R, C
Added:
1/18/2021
Last Updated:
2/11/2021

Operations

Publications

Chang Y, Allen C, Wan C, Chung D, Zhang C, Li Z, Ma Q. IRIS-FGM: an integrative single-cell RNA-Seq interpretation system for functional gene module analysis. Unknown Journal. 2020. doi:10.1101/2020.11.04.369108.