Evidence map›Paper›PMID 40581358›Full record

ArticleBioinformatics (Oxford, England)2025

SeuratIntegrate: an R package to facilitate the use of integration methods with Seurat.

Florian Specque, Aurélien Barré, Macha Nikolski, Domitille Chalopin

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
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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.

Florian SpecqueCNRS UMR 5095, IBGC, Biological and Medical Sciences Department, University of Bordeaux, Bordeaux F-33000, France.ORCID 0000-0002-4449-6381
Aurélien BarréBordeaux Bioinformatics Center (CBiB), University of Bordeaux, Bordeaux 33076, France.ORCID 0009-0006-4773-3369
Macha NikolskiCNRS UMR 5095, IBGC, Biological and Medical Sciences Department, University of Bordeaux, Bordeaux F-33000, France.ORCID 0000-0001-6059-577X
Domitille ChalopinCNRS UMR 5095, IBGC, Biological and Medical Sciences Department, University of Bordeaux, Bordeaux F-33000, France.ORCID 0000-0003-0588-9630

Funding

Agence Nationale de la RechercheInstitut National du Cancer
6 · The paper itself

Abstract

motivationIntegrating multiple datasets has become an increasingly common task in scRNA-seq analysis. The advent of single-cell atlases adds further complexity, as they often involve combining data with nested batch effects. While common tools such as Seurat offer access to batch-correction methods, the diversity of available options remains limited. With growing evidence that integration method performance varies significantly between datasets, making an informed decision in selecting the most appropriate integration approach is not trivial. A broader range of accessible methods combined with a comprehensive toolbox for comparative integration analysis, would support more effective and flexible single-cell data integration workflows.

resultsBuilt on Seurat's foundations, we developed SeuratIntegrate, an open source R package that expands integration methods available to Seurat users, including Python-based approaches, while operating entirely within the R environment. The package enables integration benchmarking using well-established performance metrics, and provides automated Python environment management, cross-language object conversion, and tools for score handling and visualization. All features are designed for ease of use and extensibility. AVAILABILITY AND IMPLEMENTATION: The source code, installation process and vignettes demonstrating usage are freely available on GitHub: https://github.com/cbib/Seurat-Integrate. A Zenodo deposit contains a copy of the package code along with the data to reproduce the results presented above (accession 10.5281/zenodo.14288360). The package is released under the MIT License.

Indexed as

Computational BiologyRNA-SeqSingle-Cell AnalysisSoftware

Identifiers

PMID40581358
PMCPMC12206523

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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.