Evidence map›Paper›PMID 41959340›Full record

ArticlebioRxiv : the preprint server for biology2026

Cell type-specific gene regulatory network inference from single cell transcriptomics with ctOTVelo.

Seowon Chang, Wenjun Zhao, Ying Ma, Bjorn Sandstede, Ritambhara Singh

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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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0cells of the map it votes in
0citing papers in PubMed
–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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Seowon ChangCenter for Computational Molecular Biology, Brown University, Providence, RI 02912.
Wenjun ZhaoDepartment of Mathematics, Wake Forest University, Winston-Salem, NC 27109.ORCID 0000-0001-7499-0084
Ying MaDepartment of Biostatistics, Center for Computational Molecular Biology, Brown University, Providence, RI 02912.ORCID 0000-0003-3791-7018
Bjorn SandstedeDepartment of Applied Mathematics, Brown University, Providence, RI 02912.
Ritambhara SinghCenter for Computational Molecular Biology, Brown University, Providence, RI 02912.

Funding

Predoctoral Training Program in Biological Data Science at Brown UniversityT32GM149433 · NIGMS · BROWN UNIVERSITY · PI Emilia Huerta-Sanchez, Sohini Ramachandran · 2024 to 2026
$976k
NIGMS NIH HHS T32 GM149433
6 · The paper itself

Abstract

Inferring gene regulatory networks (GRNs) from gene expression is a crucial task for understanding functional relationships. Gene expression data (transcriptomics) provide a snapshot of gene activity, encoding information about gene regulatory relationships. However, gene regulation is a dynamic process, modulating across time and with different cell types. Temporal GRN inference methods aim to capture these dynamics by utilizing time-stamped transcriptomics, gene expression data of similar samples captured across discrete timepoints, or pseudotime transcriptomics, computationally ordering cells based on an inferred trajectory. These methods can estimate constant or temporal gene regulatory relationships, but may not capture finer, cell type specific relationships. We propose ctOTVelo, an extension to our previous work to account for cell type specificity during GRN inference. ctOTVelo incorporates cell type labels or proportions when inferring the GRN from single cell transcriptomics data. Our methods achieve state-of-the-art performance in GRN prediction in time-stamped and pseudotime-stamped transcriptomics. Furthermore, ctOTVelo is able to generate cell type specific GRNs, allowing cell type resolution analysis of gene regulatory relationships.

Identifiers

PMID41959340
PMCPMC13060787

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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.