Evidence map›Paper›PMID 40627366›Full record

ArticleGigaScience2025

SeuratExtend: streamlining single-cell RNA-seq analysis through an integrated and intuitive framework.

Yichao Hua, Linqian Weng, Fang Zhao, Florian Rambow

Abstract read
In one paragraph

Article in GigaScience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

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

39 citing papers in PubMed.

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  12. bioRxiv : the preprint server for biology · 2026
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  17. Rational redesign of antigen binding domain improves in vivo efficacy of the CD22-CAR.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
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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

4 authors.

Yichao HuaDepartment of Applied Computational Cancer Research, Institute for AI in Medicine (IKIM), University Hospital Essen, Essen 45131, Germany.ORCID 0000-0002-1695-172X
Linqian WengDepartment of Oncology, KU Leuven, Leuven 3000, Belgium.ORCID 0000-0003-0965-4994
Fang ZhaoUniversity Duisburg-Essen, Essen 45141, Germany.ORCID 0000-0002-2746-9242
Florian RambowDepartment of Applied Computational Cancer Research, Institute for AI in Medicine (IKIM), University Hospital Essen, Essen 45131, Germany.ORCID 0000-0002-9727-8986

Funding

Melanoma Research Alliance
6 · The paper itself

Abstract

Single-cell RNA sequencing (scRNA-seq) has revolutionized the study of cellular heterogeneity, but the rapid expansion of analytical tools has proven to be both a blessing and a curse, presenting researchers with significant challenges. Here, we present SeuratExtend, a comprehensive R package built upon the widely adopted Seurat framework, which streamlines scRNA-seq data analysis by strategically integrating essential tools and databases. SeuratExtend offers a user-friendly and intuitive interface for performing a wide range of analyses, including functional enrichment, trajectory inference, gene regulatory network reconstruction, and denoising. The package integrates multiple databases, such as Gene Ontology and Reactome, and incorporates popular Python tools like scVelo, Palantir, and SCENIC through a unified R interface. We illustrate SeuratExtend's capabilities through case studies investigating tumor-associated high-endothelial venules and autoinflammatory diseases, as well as showcase its novel applications in pathway-level analysis and cluster annotation. SeuratExtend enhances data visualization with optimized plotting functions and carefully curated color schemes, ensuring both aesthetic appeal and scientific rigor. The package's effectiveness has been demonstrated through successful workshops and training programs, establishing its value in both research and educational contexts. SeuratExtend empowers researchers to harness the full potential of scRNA-seq data, making complex analyses accessible to a wider audience. The package, along with comprehensive documentation, tutorials, and educational resources, is freely available at GitHub, providing a valuable resource for the single-cell genomics community.

Indexed as

Computational BiologyRNA-SeqSequence Analysis, RNASingle-Cell AnalysisSoftwareGene Regulatory NetworksHumansSingle-Cell Gene Expression Analysisbioinformaticseducationmultitool integrationpathway analysisR packageSeurat frameworksingle-cell RNA-seqvisualization

Identifiers

PMID40627366
PMCPMC12236070

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.