Evidence map›Paper›PMID 42635227›Full record

ArticleBioinformatics (Oxford, England)2026

Sensitivity analysis of cell fate trajectories from single-cell transcriptomics.

Abdullah Al Noman, Palash Sashittal

Abstract read
In one paragraph

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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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Abdullah Al NomanDepartment of Computer Science, Virginia Tech, Blacksburg, VA 24060, United States.ORCID 0000-0003-3738-264X
Palash SashittalDepartment of Computer Science, Virginia Tech, Blacksburg, VA 24060, United States.ORCID 0000-0001-6581-4839

Funding

Virginia Tech
6 · The paper itself

Abstract

summaryCell differentiation is a dynamic process in which cells traverse through high-dimensional gene expression space under the influence of gene regulatory networks and environmental cues. Recent advances in single-cell RNA sequencing (scRNA-seq) have enabled us to measure high-resolution snapshots of this dynamic process. Several computational methods have been developed to reconstruct cellular flow maps from these snapshots, revealing the trajectories taken by cells in gene expression space. While existing methods provide increasingly detailed descriptions of cellular trajectories, the stability of these trajectories to perturbations is largely unexplored. As such, it remains unclear how robust inferred trajectories are to perturbations, which genes most strongly influence long-term fate outcomes, and where instability arises between competing fate commitments. While sensitivity and stability analysis tools from dynamical systems theory provide a principled way to study the stability of differentiation trajectories, existing approaches are not designed for the high-dimensionality and sparsity of scRNA-seq data. Here, we introduce FateSens, a sensitivity-based computational framework for analyzing gene regulatory dynamics using flow maps derived from scRNA-seq data. FateSens performs sensitivity analysis of differentiation trajectories derived from scRNA-seq data to identify regulatory genes and fate boundaries. To demonstrate its utility, we applied FateSens to study neutrophil-monocyte differentiation using scRNA-seq data of mouse hematopoiesis. While FateSens relies only on transcriptomic measurements, this dataset also contains lineage tracing barcodes that provide ground-truth fate relationships. Our results show that FateSens accurately recovers regulators consistent with known biology and identifies fate boundaries that are supported by lineage tracing data. AVAILABILITY AND IMPLEMENTATION: We implement FateSens in Python 3, with an open-source implementation available at: https://github.com/sashittal-group/FateSens.

Indexed as

Cell DifferentiationComputational BiologyGene Expression ProfilingSingle-Cell AnalysisTranscriptomeAnimalsGene Regulatory NetworksMiceSequence Analysis, RNASingle-Cell Gene Expression Analysis

Identifiers

PMID42635227
PMCPMC13501315

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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.