SCIG: Machine learning uncovers cell identity genes in single cells by genetic sequence codes

Deciphering cell identity genes is pivotal to understanding cell differentiation, development, and cell identity dysregulation involving diseases. Here, we introduce SCIG, a machine-learning method to uncover cell identity genes in single cells. In alignment with recent reports that cell identity genes (CIGs) are regulated with unique epigenetic signatures, we found CIGs exhibit distinctive genetic sequence signatures, e.g. unique enrichment patterns of cis-regulatory elements. Using these genetic sequence signatures, along with gene expression information from single-cell RNA-seq data, SCIG uncovers the identity genes of a cell without a need for comparison to other cells. CIG score defined by SCIG surpassed expression value in network analysis to reveal the master transcription factors (TFs) regulating cell identity. Applying SCIG to the human endothelial cell atlas revealed that the tissue microenvironment is a critical supplement to master TFs for cell identity refinement. SCIG is publicly available at https://doi.org/10.5281/zenodo.14726426 , offering a valuable tool for advancing cell differentiation, development, and regenerative medicine research.

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Publication Details

Journal
Nucleic Acids Research
Published
2025-05-22
DOI
https://doi.org/10.1093/nar/gkaf431
Citations
2
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
1.61

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article

SCIG: Machine learning uncovers cell identity genes in single cells by genetic sequence codes

Yang Yu, Kaifu Chen, A. Kulandaisamy, Hong Chen et al.
2 citations
Nucleic Acids Research
Single-cell and spatial transcriptomics
1.61
article

SCIG: Machine learning uncovers cell identity genes in single cells by genetic sequence codes

Yang Yu, Kaifu Chen, A. Kulandaisamy, Hong Chen, William T. Pu, Lili Zhang, Bo Xia
article en
2 citations

Abstract

Deciphering cell identity genes is pivotal to understanding cell differentiation, development, and cell identity dysregulation involving diseases. Here, we introduce SCIG, a machine-learning method to uncover cell identity genes in single cells. In alignment with recent reports that cell identity genes (CIGs) are regulated with unique epigenetic signatures, we found CIGs exhibit distinctive genetic sequence signatures, e.g. unique enrichment patterns of cis-regulatory elements. Using these genetic sequence signatures, along with gene expression information from single-cell RNA-seq data, SCIG uncovers the identity genes of a cell without a need for comparison to other cells. CIG score defined by SCIG surpassed expression value in network analysis to reveal the master transcription factors (TFs) regulating cell identity. Applying SCIG to the human endothelial cell atlas revealed that the tissue microenvironment is a critical supplement to master TFs for cell identity refinement. SCIG is publicly available at https://doi.org/10.5281/zenodo.14726426 , offering a valuable tool for advancing cell differentiation, development, and regenerative medicine research.

Nucleic Acids ResearchVol. 53(10)
Boston Children's Hospital (US), Harvard University (US), Boston Children's Museum (US), Clemson University (US)
National Institutes of Health
Openalex Percentile: Top 17%
Single-cell and spatial transcriptomics
1.61
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SCIG: Machine learning uncovers cell identity genes in single cells by genetic sequence codes — Yang Yu, Kaifu Chen, et al. · Nucleic Acids Research (2025) | TGRS Research Map | TGRS