Evidence map›Paper›PMID 40968359›Full record

ArticleGenome biology2025

Systematic benchmarking of computational methods to identify spatially variable genes.

Zhijian Li, Zain M Patel, Dongyuan Song, Sai Nirmayi Yasa, Robrecht Cannoodt, Guanao Yan, Jingyi Jessica Li, Luca Pinello

Abstract read
In one paragraph

Article in Genome biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

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  10. Artificial Intelligence Revolution in Transcriptomics: From Single Cells to Spatial Atlases.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Zhijian Li *Gene Regulatory Observatory, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Zain M Patel *Gene Regulatory Observatory, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Dongyuan SongDepartment of Genetics and Genome Sciences, University of Connecticut Health Center, Farmington, CT, USA.
Sai Nirmayi YasaData Intuitive, Lebbeke, Belgium.
Robrecht CannoodtData Intuitive, Lebbeke, Belgium.
Guanao YanDepartment of Statistics and Data Science, University of California, Los Angeles, CA, USA.
Jingyi Jessica LiDepartment of Statistics and Data Science, University of California, Los Angeles, CA, USA.
Luca PinelloGene Regulatory Observatory, Broad Institute of MIT and Harvard, Cambridge, MA, USA. lpinello@mgh.harvard.edu.

Funding

Multiscale exploration of the functional non-coding genomeR35HG010717 · NHGRI · MASSACHUSETTS GENERAL HOSPITAL · PI PINELLO, LUCA · 2019 to 2023
$2.6M
National Human Genome Research Institute (NHGRI) 1R35HG010717-01NHGRI NIH HHS R35 HG010717
6 · The paper itself

Abstract

backgroundSpatially resolved transcriptomics offers unprecedented insight by enabling the profiling of gene expression within the intact spatial context of cells, effectively adding a new and essential dimension to data interpretation. To efficiently detect spatial structure of interest, an essential step in analyzing such data involves identifying spatially variable genes (SVGs). Despite researchers having developed several computational methods to accomplish this task, the lack of a comprehensive benchmark evaluating their performance remains a considerable gap in the field.

resultsHere, we systematically evaluate 14 methods using 96 spatial datasets and 6 metrics. We compare the methods regarding gene ranking and classification based on real spatial variation, statistical calibration, and computation scalability and investigate the impact of identified SVGs on downstream applications such as spatial domain detection. Finally, we explore the applicability of the methods to spatial ATAC-seq data to examine their effectiveness in identifying spatially variable peaks (SVPs). Overall, SPARK-X outperforms other benchmarked methods and Moran's I achieves a competitive performance, representing a strong baseline for future method development. Moreover, our results reveal that most methods are poorly calibrated, and more specialized algorithms are needed to identify spatially variable peaks.

conclusionsOur benchmarking provides a detailed comparison of SVG detection methods and serves as a reference for both users and method developers.

Indexed as

BenchmarkingComputational BiologyGene Expression ProfilingAlgorithmsHumansTranscriptomeBenchmarkingMERFISHSimulationSpatially variable genesSpatial omicsVisium

Identifiers

PMID40968359
PMCPMC12445034

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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.