Evidence map›Paper›PMID 41219206›Full record

ArticleNature communications2025

ELLA: modeling subcellular spatial variation of gene expression within cells in high-resolution spatial transcriptomics.

Jade Xiaoqing Wang, Xiang Zhou

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Jade Xiaoqing WangDepartment of Statistics, Texas A&M University, College Station, TX, USA.
Xiang ZhouDepartment of Statistics and Data Science, Yale University, New Haven, CT, USA. xiang.zhou.xz735@yale.edu.ORCID http://orcid.org/0000-0002-4331-7599

Funding

Statistical Methods for Modeling Polygenic Architecture in Association and Re-sequencing StudiesR01HG009124 · NHGRI · YALE UNIVERSITY · PI Xiang Zhou · 2017 to 2026
$3.0M
New directions in single cell genomics method developmentR01GM126553 · NIGMS · UNIVERSITY OF CHICAGO · PI Mengjie Chen · 2017 to 2026
$2.9M
Develop new bioinformatics infrastructures and computational tools for epitranscriptomics dataR01HG012927 · NHGRI · UNIVERSITY OF CHICAGO · PI Mengjie Chen · 2023 to 2026
$1.6M
Developing new computational tools for spatial transcriptomics dataR01HG011883 · NHGRI · UNIVERSITY OF CHICAGO · PI CHEN, MENGJIE, ZHOU, XIANG · 2021 to 2024
$1.5M
DMS/NIGMS 2: Advanced Statistical Methods for Spatially Resolved Transcriptomics StudiesR01GM144960 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZHOU, XIANG · 2021 to 2024
$1.3M
NHGRI NIH HHS R01 HG009124NHGRI NIH HHS R01 HG011883NHGRI NIH HHS R01 HG012927NIGMS NIH HHS R01 GM126553NIGMS NIH HHS R01 GM144960U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI) R01HG009124U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI) R01HG011883U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R01GM126553U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R01GM144960
6 · The paper itself

Abstract

Spatial transcriptomics technologies are becoming increasingly high-resolution, enabling gene expression measurement at the subcellular level. Here, we present subcellular expression localization analysis (ELLA), a statistical framework for modeling subcellular mRNA localization and detecting spatially variable genes within cells. ELLA uses an over-dispersed nonhomogeneous Poisson process to model spatial count data with a unified cellular coordinate system to anchor diverse cellular morphologies, demonstrating effective type I error control and high power in simulations. In real data applications, ELLA identifies genes with distinct subcellular localization and associate these patterns to key mRNA characteristics: nuclear-enriched genes exhibit an abundance of long noncoding RNAs or protein-coding mRNAs, while cytoplasmic- or membrane-enriched genes frequently encode ribosomal proteins or contain signal peptides. ELLA also uncovers dynamic subcellular localization changes across the cell cycle. Overall, ELLA is a powerful, robust, and scalable tool for subcellular spatial expression analysis across high-resolution spatial transcriptomics platforms.

Indexed as

Gene Expression ProfilingTranscriptomeCell CycleCell NucleusHumansRNA, Long NoncodingRNA, MessengerRNA, Long NoncodingRNA, Messenger

Identifiers

PMID41219206
PMCPMC12606177

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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 OpenQuestion graph.