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Abstract

Single-cell RNA-seq allows building cell atlases of any given tissue and infer the dynamics of cellular state transitions during developmental or disease trajectories. Both the maintenance and transitions of cell states are encoded by regulatory programs in the genome sequence. However, this regulatory code has not yet been exploited to guide the identification of cellular states from single-cell RNA-seq data. Here we describe a computational resource, called SCENIC (Single Cell rEgulatory Network Inference and Clustering), for the simultaneous reconstruction of gene regulatory networks (GRNs) and the identification of stable cell states, using single-cell RNA-seq data. SCENIC outperforms existing approaches at the level of cell clustering and transcription factor identification. Importantly, we show that cell state identification based on GRNs is robust towards batch-effects and technical-biases. We applied SCENIC to a compendium of single-cell data from the mouse and human brain and demonstrate that the proper combinations of transcription factors, target genes, enhancers, and cell types can be identified. Moreover, we used SCENIC to map the cell state landscape in melanoma and identified a gene regulatory network underlying a proliferative melanoma state driven by MITF and STAT and a contrasting network controlling an invasive state governed by NFATC2 and NFIB. We further validated these predictions by showing that two transcription factors are predominantly expressed in early metastatic sentinel lymph nodes. In summary, SCENIC is the first method to analyze scRNA-seq data using a network-centric, rather than cell-centric approach. SCENIC is generic, easy to use, and flexible, and allows for the simultaneous tracing of genomic regulatory programs and the mapping of cellular identities emerging from these programs. Availability: SCENIC is available as an R workflow based on three new R/Bioconductor packages: GENIE3, RcisTarget and AUCell. As scalable alternative to GENIE3, we also provide GRNboost, paving the way towards the network analysis across millions of single cells.

Abstract summary

Claude Opus 5.5 · max effort · 17 Oct 2026 · from the abstract

Building gene regulatory networks from scRNA-seq and clustering cells on them identifies stable states robustly to batch effects, applied to mouse and human brain and to melanoma.

Cell states are set by regulatory programs written in the genome, yet scRNA-seq clustering has ignored that code and grouped cells on expression alone. SCENIC reconstructs transcription factor networks and uses them as the basis for defining cell states, a network-centric rather than cell-centric way of analysing scRNA-seq.

Key results

  1. ClaimedClustering cells on inferred regulatory networks beats existing approaches at both cell clustering and transcription factor identification, and the resulting states resist batch effects and technical bias.

    Stated as an outcome of comparisons in the abstract, which names no competing methods, metrics or benchmark datasets. · Abstract

  2. SuggestedOn a compendium of mouse and human brain single-cell data, the method recovered coherent sets of transcription factors, target genes, enhancers and cell types.

    Reported as a demonstration; the abstract gives no cell numbers, dataset names or accuracy measures for the recovered combinations. · Abstract

  3. SuggestedIn melanoma the method separated a proliferative and an invasive state with distinct regulatory networks, and, as validation, two transcription factors were shown to be mainly expressed in early metastatic sentinel lymph nodes.

    The proliferative network is driven by MITF and STAT, the invasive one by NFATC2 and NFIB; the abstract does not name the two transcription factors shown to be mainly expressed in early metastatic sentinel lymph nodes or say how this was measured. · Abstract

Methods, data and reproducibility

A workflow that infers gene regulatory networks linking transcription factors to target genes from scRNA-seq and simultaneously uses those networks to identify stable cell states, shifting clustering from a cell-centric to a network-centric basis.

  • Compendium of brain single-cell RNA-seq data · mouse and human
  • Melanoma single-cell data used to map the cell state landscape
  • Early metastatic sentinel lymph nodes used to check transcription factor expression
Methods & tools
SCENIC, GENIE3, RcisTarget, AUCell, GRNboost, R/Bioconductor
Reagents & environment
An R workflow built on three R/Bioconductor packages, GENIE3, RcisTarget and AUCell, with GRNboost offered as a scalable alternative to GENIE3.
Reproducibility gaps
No repository link, package version or dataset accession appears in the abstract.
Limitations (2)
  • The claimed advantage over existing clustering and transcription factor identification methods comes without named baselines, metrics or benchmark datasets. · noted in this summary
  • Validation covers the expression of two transcription factors in sentinel lymph nodes, which does not test the inferred network edges themselves. · noted in this summary

Read this if you want cell states defined by transcription factor regulatory networks, or need cell state identification that is robust to batch effects and technical biases.

Citations
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