Evidence map›Paper›PMID 38580861›Full record

ArticleNature biotechnology2025

Gene trajectory inference for single-cell data by optimal transport metrics.

Rihao Qu, Xiuyuan Cheng, Esen Sefik, Jay S Stanley Iii, Boris Landa, Francesco Strino, Sarah Platt, James Garritano, Ian D Odell, Ronald Coifman and 3 more

Abstract read
In one paragraph

Article in Nature biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Rihao Qu *Computational Biology & Bioinformatics Program, Yale University, New Haven, CT, USA.
Xiuyuan Cheng *Department of Mathematics, Duke University, Durham, NC, USA.
Esen SefikDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0002-6807-3498
Jay S Stanley IiiProgram in Applied Mathematics, Yale University, New Haven, CT, USA.
Boris LandaProgram in Applied Mathematics, Yale University, New Haven, CT, USA.
Francesco StrinoPCMGF Limited, Watford, UK.ORCID http://orcid.org/0000-0002-9310-4794
Sarah PlattDepartment of Pathology, Yale University School of Medicine, New Haven, CT, USA.
James GarritanoProgram in Applied Mathematics, Yale University, New Haven, CT, USA.
Ian D OdellDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT, USA.
Ronald CoifmanProgram in Applied Mathematics, Yale University, New Haven, CT, USA.
Richard A FlavellDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0003-4461-0778
Peggy MyungDepartment of Pathology, Yale University School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0002-2970-4170
Yuval KlugerComputational Biology & Bioinformatics Program, Yale University, New Haven, CT, USA. yuval.kluger@yale.edu.ORCID http://orcid.org/0000-0002-3035-071X

Funding

Yale SPORE in Skin CancerP50CA121974 · NCI · YALE UNIVERSITY · PI MARCUS W BOSENBERG, Harriet M. Kluger · 2006 to 2026
$43.9M
The Y-SCORCH Data Generation Center at Yale for Single-Cell Opioid Responses in the Context of HIVUM1DA051410 · NIDA · YALE UNIVERSITY · PI GERSTEIN, MARK BENDER, KLUGER, YUVAL · 2020 to 2025
$15.3M
M-SCORCH: Methamphetamine use disorder data generation center for Single Cell Opioid Responses in the Context of HIVU01DA053628 · NIDA · YALE UNIVERSITY · PI HO, YA-CHI, SESTAN, NENAD · 2021 to 2025
$9.5M
Yale TMC for Cellular Senescence in Lymphoid OrgansU54AG076043 · NIA · YALE UNIVERSITY · PI HALENE, STEPHANIE · 2021 to 2025
$7.0M
Yale Murine-TMC on Immune Cell Senescence Derived InflammationU54AG079759 · NIA · YALE UNIVERSITY · PI DIXIT, VISHWA DEEP, MONTGOMERY, RUTH R · 2022 to 2025
$6.5M
Role of clonal expansion in HIV-1 persistenceR01AI141009 · NIAID · YALE UNIVERSITY · PI Ya-Chi Ho · 2018 to 2026
$5.3M
Delineating spatiotemporal dynamics of hair follicle dermal niche specification at the single-cell levelR01AR076420 · NIAMS · YALE UNIVERSITY · PI MYUNG, PEGGY S · 2020 to 2024
$1.8M
EFFICIENT METHODS FOR CALIBRATION, CLUSTERING, VISUALIZATION AND IMPUTATION OF LARGE scRNA-seq DATAR01GM131642 · NIGMS · YALE UNIVERSITY · PI KLUGER, YUVAL · 2019 to 2022
$1.6M
Epidermal Growth Factor Receptor Signaling in Fibrotic Skin DiseaseK08AR077689 · NIAMS · YALE UNIVERSITY · PI ODELL, IAN D · 2021 to 2025
$861k
Interrogation of T cell Bystander Activation in SclerodermaR03AR083454 · NIAMS · YALE UNIVERSITY · PI ODELL, IAN D · 2024 to 2024
$147k
NCI NIH HHS P50 CA121974NIAID NIH HHS R01 AI141009NIAMS NIH HHS K08 AR077689NIAMS NIH HHS R01 AR076420NIAMS NIH HHS R03 AR083454NIA NIH HHS U54 AG076043NIA NIH HHS U54 AG079759NIDA NIH HHS U01 DA053628NIDA NIH HHS UM1 DA051410NIGMS NIH HHS R01 GM131642NSF | Directorate for Mathematical & Physical Sciences | Division of Mathematical Sciences (DMS) DMS-223784U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) P50CA121974U.S. Department of Health & Human Services | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) R01AR076420U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R01GM131642U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) U54AG076043U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) U54AG079759U.S. Department of Health & Human Services | NIH | National Institute on Drug Abuse (NIDA) U01DA053628U.S. Department of Health & Human Services | NIH | National Institute on Drug Abuse (NIDA) UM1DA051410
6 · The paper itself

Abstract

Single-cell RNA sequencing has been widely used to investigate cell state transitions and gene dynamics of biological processes. Current strategies to infer the sequential dynamics of genes in a process typically rely on constructing cell pseudotime through cell trajectory inference. However, the presence of concurrent gene processes in the same group of cells and technical noise can obscure the true progression of the processes studied. To address this challenge, we present GeneTrajectory, an approach that identifies trajectories of genes rather than trajectories of cells. Specifically, optimal transport distances are calculated between gene distributions across the cell-cell graph to extract gene programs and define their gene pseudotemporal order. Here we demonstrate that GeneTrajectory accurately extracts progressive gene dynamics in myeloid lineage maturation. Moreover, we show that GeneTrajectory deconvolves key gene programs underlying mouse skin hair follicle dermal condensate differentiation that could not be resolved by cell trajectory approaches. GeneTrajectory facilitates the discovery of gene programs that control the changes and activities of biological processes.

Indexed as

Sequence Analysis, RNASingle-Cell AnalysisAlgorithmsAnimalsCell DifferentiationCell LineageGene Expression ProfilingHair FollicleMice

Identifiers

PMID38580861
PMCPMC11452571

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Registered trials

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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.