Evidence map›Paper›PMID 42209442›Full record

ArticleBioinformatics (Oxford, England)2026

PathwayEmbed: a computational tool to quantify intracellular signaling transduction states from transcriptomic data.

Yaqing Huang, Sharon Gerecht, Themis Kyriakides, Micha Sam Brickman Raredon

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Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Yaqing HuangDepartment of Pathology, Yale University, New Haven, CT 06520, United States.
Sharon GerechtBiomedical Engineering, Duke University, Durham, NC 27705, United States.
Themis KyriakidesDepartment of Pathology, Yale University, New Haven, CT 06520, United States.
Micha Sam Brickman RaredonVascular Biology and Therapeutics Program, Yale University, New Haven, CT 06520, United States.ORCID 0000-0003-1441-6122

Funding

American Heart Association 26POST1553068National Institute of General Medical Sciences (NIGMS) T32GM086287NIGMS, NIHUnited States governmentYale School of Medicine and the Yale Department of Anesthesiology
6 · The paper itself

Abstract

motivationIntracellular signaling pathways regulate essential cellular functions and orchestrate complex biological processes, yet their dynamic activity remains challenging to quantify with precision. Advances in single-cell omics enable pathway activity inference at the transcriptional level; however, existing computational tools often overlook mechanistic features of signaling networks, failing to formally treat the expected directionality of transcriptional change due to signal transduction. To address this technological gap, we have engineered PathwayEmbed, an R-based computational framework for estimating intracellular signal transduction states from single-cell transcriptomic datasets.

resultsPathwayEmbed integrates KEGG pathway information with perturbation-derived RNA sequencing data to assign directional coefficients that capture gene-specific transcriptional responses to pathway activation, repression, and/or signal transduction. These coefficients, in combination with the input data, are used to compute hypothetic ON/OFF range for each pathway. Each cell is then mapped to a specific location between these ON/OFF states, and activity scores are then computed based on the distances to these reference states, providing a continuous and interpretable measure of signaling activity at single-cell resolution. This framework enables robust visualization and quantitative comparison of pathway activity across cell populations. Applied to spatial transcriptomic data, PathwayEmbed captures spatial variation in signaling transduction states and allows comparisons at both temporal and spatial scale. The framework takes tabular data as input and is broadly compatible with established single-cell analysis workflows, supports user-defined pathway ground-truths, and offers a flexible, mechanistically informed approach for quantifying and comparing intracellular signaling activity in a wide variety of contexts. AVAILABILITY: PathwayEmbed is an open-source R software under academic free license, and it is available at https://github.com/raredonlab/PathwayEmbed. Use-case vignettes are available at https://raredonlab.github.io/PathwayEmbed/.

Indexed as

Computational BiologySignal TransductionSingle-Cell Gene Expression AnalysisSoftwareTranscriptome

Identifiers

PMID42209442
PMCPMC13292150

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.