Evidence map›Paper›PMID 38844627›Full record

ArticleNature methods2024

Accurate and efficient integrative reference-informed spatial domain detection for spatial transcriptomics.

Ying Ma, Xiang Zhou

Abstract read
In one paragraph

Article in Nature methods, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 1 pooled it
–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

54 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

2 authors.

Ying MaDepartment of Biostatistics, Brown University, Providence, RI, USA.ORCID http://orcid.org/0000-0003-3791-7018
Xiang ZhouDepartment of Biostatistics, University of Michigan, Ann Arbor, MI, USA. xzhousph@umich.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) 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

Spatially resolved transcriptomics (SRT) studies are becoming increasingly common and large, offering unprecedented opportunities in mapping complex tissue structures and functions. Here we present integrative and reference-informed tissue segmentation (IRIS), a computational method designed to characterize tissue spatial organization in SRT studies through accurately and efficiently detecting spatial domains. IRIS uniquely leverages single-cell RNA sequencing data for reference-informed detection of biologically interpretable spatial domains, integrating multiple SRT slices while explicitly considering correlations both within and across slices. We demonstrate the advantages of IRIS through in-depth analysis of six SRT datasets encompassing diverse technologies, tissues, species and resolutions. In these applications, IRIS achieves substantial accuracy gains (39-1,083%) and speed improvements (4.6-666.0) in moderate-sized datasets, while representing the only method applicable for large datasets including Stereo-seq and 10x Xenium. As a result, IRIS reveals intricate brain structures, uncovers tumor microenvironment heterogeneity and detects structural changes in diabetes-affected testis, all with exceptional speed and accuracy.

Indexed as

Single-Cell AnalysisTranscriptomeAnimalsBrainComputational BiologyGene Expression ProfilingHumansMaleMiceSequence Analysis, RNATestis

Identifiers

PMID38844627
PMCPMC11831598

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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.