Evidence map›Paper›PMID 40515599›Full record

ArticleBiostatistics (Oxford, England)2025

Addressing the mean-variance relationship in spatially resolved transcriptomics data with spoon.

Kinnary Shah, Boyi Guo, Stephanie C Hicks

Abstract read
In one paragraph

Article in Biostatistics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Kinnary ShahDepartment of Biostatistics, Johns Hopkins Bloomberg School of Public Health, 615 N Wolfe Street, Baltimore, MD 21205, United States.ORCID 0000-0001-7098-2116
Boyi GuoDepartment of Biostatistics, Johns Hopkins Bloomberg School of Public Health, 615 N Wolfe Street, Baltimore, MD 21205, United States.ORCID 0000-0003-2950-2349
Stephanie C HicksDepartment of Biostatistics, Johns Hopkins Bloomberg School of Public Health, 615 N Wolfe Street, Baltimore, MD 21205, United States.ORCID 0000-0002-7858-0231

Funding

Laminar dissection of cortical human brain gene expression in neuropsychiatric disordersR01MH126393 · NIMH · LIEBER INSTITUTE, INC. · PI MARTINOWICH, KERI · 2021 to 2025
$3.9M
Registration of spatial gene expression in key nodes of reward-related circuitry in the human brainR01DA053581 · NIDA · LIEBER INSTITUTE, INC. · PI MARTINOWICH, KERI · 2021 to 2025
$3.7M
Characterization of high-grade serous ovarian cancer subtypes via single-cell profilingR01CA237170 · NCI · UNIVERSITY OF PENNSYLVANIA · PI DOHERTY, JENNIFER A., GREENE, CASEY S · 2019 to 2024
$3.0M
Chan ZuckerbergNCI NIH HHS R01 CA237170NIDA NIH HHS R01 DA053581NIH HHS R01CA237170NIH HHS R01DA053581NIH HHS R01MH126393NIMH NIH HHS R01 MH126393Silicon Valley Community Foundation CZF2019-002443
6 · The paper itself

Abstract

An important task in the analysis of spatially resolved transcriptomics (SRT) data is to identify spatially variable genes (SVGs), or genes that vary in a 2D space. Current approaches rank SVGs based on either $ P $-values or an effect size, such as the proportion of spatial variance. However, previous work in the analysis of RNA-sequencing data identified a technical bias with log-transformation, violating the "mean-variance relationship" of gene counts, where highly expressed genes are more likely to have a higher variance in counts but lower variance after log-transformation. Here, we demonstrate the mean-variance relationship in SRT data. Furthermore, we propose spoon, a statistical framework using empirical Bayes techniques to remove this bias, leading to more accurate prioritization of SVGs. We demonstrate the performance of spoon in both simulated and real SRT data. A software implementation of our method is available at https://bioconductor.org/packages/spoon.

Indexed as

Gene Expression ProfilingSoftwareTranscriptomeBayes TheoremData Interpretation, StatisticalHumansSequence Analysis, RNAempirical BayesGaussian process regressionmean–variance biasspatially variable genespatial transcriptomics

Identifiers

PMID40515599
PMCPMC12166475

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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.