Evidence map›Paper›PMID 42461016›Full record

ArticleBioinformatics (Oxford, England)2026

BatchSVG: identifying batch-biased genes in the application of spatially variable gene detection.

Kinnary Shah, Christine Hou, Jacqueline R Thompson, Stephanie C Hicks

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Kinnary ShahDepartment of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, United States.ORCID 0000-0001-7098-2116
Christine HouDepartment of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, United States.ORCID 0009-0001-5350-0629
Jacqueline R ThompsonDepartment of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, United States.ORCID 0000-0002-1365-8536
Stephanie C HicksDepartment of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, United States.ORCID 0000-0002-7858-0231

Funding

Computational Methods for Emerging Spatially-resolved Transcriptomics with Multiple SamplesR35GM150671 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI Stephanie Carinne Hicks · 2023 to 2026
$1.2M
National Institutes of Health/National Institute of General Medical Sciences R35GM150671NIGMS NIH HHS R35 GM150671
6 · The paper itself

Abstract

summaryA standard task in the analysis of spatially resolved transcriptomics (SRT) data is to identify spatially variable genes (SVGs). This is most commonly done within one tissue section at a time because the spatial relationships between the tissue sections are typically unknown. However, large-scale spatial atlases are being generated, for example across hundreds of donors, where the goal is to identify a common set of SVGs to use for downstream analyses. One challenge is how to identify and remove SVGs that are associated with a known bias or technical artifact, such as the slide, which can lead to poor performance in downstream analyses, such as spatial domain detection. Here, we introduce BatchSVG, a tool to identify batch-biased genes SVGs. Our approach compares the rank of per-gene deviance under a binomial model (i) with and (ii) without including a covariate in the model that is associated with the known bias or technical artifact. If the rank of a gene changes significantly between these models, then we infer that this gene is likely associated with the bias or technical artifact and should be removed from the downstream analyses. We consider two SRT datasets and show how our model can improve the results of downstream analyses. AVAILABILITY AND IMPLEMENTATION: The BatchSVG package is freely available at https://bioconductor.org/packages/BatchSVG, and the code to reproduce the figures is publicly available at https://github.com/kinnaryshah/BatchSVG-analyses.

Indexed as

Computational BiologyGene Expression ProfilingSoftwareAlgorithmsAnimalsSpatial Transcriptomics

Identifiers

PMID42461016
PMCPMC13412158

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.