Evidence map›Paper›PMID 42386773›Full record

ArticleNature communications2026

Interpretable spatial multi-omics data integration and dimensionality reduction with SpaMV.

Yang Liu, Kexin Ma, Haoran Xu, Ke Xu, Yunfei Hu, Zhenhan Lin, Jiangli Lin, Bo Han, Shuaicheng Li, Zhixiang Lin and 2 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Yang LiuDepartment of Computer Science, Hong Kong Baptist University, Hong Kong SAR, China.ORCID http://orcid.org/0009-0008-0319-7239
Kexin MaCollege of Biomedical Engineering, Sichuan University, Chengdu, China.
Haoran XuCollege of Biomedical Engineering, Sichuan University, Chengdu, China.
Ke XuDepartment of Computer Science, Hong Kong Baptist University, Hong Kong SAR, China.
Yunfei HuDepartment of Computer Science, Vanderbilt University, Nashville, TN, USA.ORCID http://orcid.org/0009-0003-7167-9620
Zhenhan LinDepartment of Computer Science, Vanderbilt University, Nashville, TN, USA.ORCID http://orcid.org/0009-0005-6061-3348
Jiangli LinCollege of Biomedical Engineering, Sichuan University, Chengdu, China.ORCID http://orcid.org/0000-0003-2030-9681
Bo HanDepartment of Computer Science, Hong Kong Baptist University, Hong Kong SAR, China.ORCID http://orcid.org/0000-0002-6338-0958
Shuaicheng LiDepartment of Computer Science, City University of Hong Kong, Hong Kong SAR, China.ORCID http://orcid.org/0000-0002-0620-9353
Zhixiang LinDepartment of Statistics, Chinese University of Hong Kong, Hong Kong SAR, China.ORCID http://orcid.org/0000-0001-9301-947X
Xin Maizie ZhouDepartment of Computer Science, Vanderbilt University, Nashville, TN, USA. maizie.zhou@vanderbilt.edu.ORCID http://orcid.org/0000-0003-4015-4787
Lu ZhangDepartment of Computer Science, Hong Kong Baptist University, Hong Kong SAR, China. ericluzhang@hkbu.edu.hk.ORCID http://orcid.org/0000-0002-2794-7371

Funding

Detecting structural variants in a large population of samples through high-throughput sequencing dataR35GM146960 · NIGMS · VANDERBILT UNIVERSITY · PI Xin Maizie Zhou · 2022 to 2026
$2.1M
Food and Health Bureau of the Government of the Hong Kong Special Administrative Region | Health and Medical Research Fund (HMRF) 11221026Hong Kong Baptist University (HKBU) RCMS/24-25/0NIEHS NIH HHS 27306C2005NIGMS NIH HHS R35 GM146960Research Grants Council, University Grants Committee (RGC, UGC) C2025-24Y
6 · The paper itself

Abstract

Spatial multi-omics technologies revolutionized our understanding of biological systems by providing spatially resolved molecular profiles from multiple perspectives. Existing spatial multi-omics integration methods often assume that data from different omics share a common underlying distribution and aim to project them into a single unified latent space. This assumption, however, obscures the unique insights offered by each omics, thereby limiting the full potential of multi-omics analyses. To address this limitation, we develop the Spatial Multi-View (SpaMV) representation learning algorithm, which explicitly captures both shared information across omics and the distinct, omics-specific information, enabling a more comprehensive and interpretable representation of spatial multi-omics data. Through extensive evaluation on both simulated and real-world datasets, SpaMV demonstrates superior spatial domain clustering performance and offers topic modeling with more interpretable dimensionality reduction for downstream analysis. Moreover, our method more effectively discovers interpretable omics-specific biomarkers than existing approaches, highlighting its strength in disentangling multi-omics signals.

Indexed as

Computational BiologyMultiomicsAlgorithmsClustering AlgorithmsComputer SimulationDimensionality ReductionGenomicsHumans

Identifiers

PMID42386773
PMCPMC13462975

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.