Evidence map›Paper›PMID 38940176›Full record

ArticleBioinformatics (Oxford, England)2024

Deciphering high-order structures in spatial transcriptomes with graph-guided Tucker decomposition.

Charles Broadbent, Tianci Song, Rui Kuang

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. 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

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

3 citing papers in PubMed.

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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

3 authors.

Charles BroadbentDepartment of Computer Science and Engineering, University of Minnesota Twin Cities, Minneapolis, MN, 55455, United States.
Tianci SongDepartment of Computer Science and Engineering, University of Minnesota Twin Cities, Minneapolis, MN, 55455, United States.
Rui KuangDepartment of Computer Science and Engineering, University of Minnesota Twin Cities, Minneapolis, MN, 55455, United States.

Funding

National Science FoundationNSF #2042159
6 · The paper itself

Abstract

Spatial transcripome (ST) profiling can reveal cells' structural organizations and functional roles in tissues. However, deciphering the spatial context of gene expressions in ST data is a challenge-the high-order structure hiding in whole transcriptome space over 2D/3D spatial coordinates requires modeling and detection of interpretable high-order elements and components for further functional analysis and interpretation. This paper presents a new method GraphTucker-graph-regularized Tucker tensor decomposition for learning high-order factorization in ST data. GraphTucker is based on a nonnegative Tucker decomposition algorithm regularized by a high-order graph that captures spatial relation among spots and functional relation among genes. In the experiments on several Visium and Stereo-seq datasets, the novelty and advantage of modeling multiway multilinear relationships among the components in Tucker decomposition are demonstrated as opposed to the Canonical Polyadic Decomposition and conventional matrix factorization models by evaluation of detecting spatial components of gene modules, clustering spatial coefficients for tissue segmentation and imputing complete spatial transcriptomes. The results of visualization show strong evidence that GraphTucker detect more interpretable spatial components in the context of the spatial domains in the tissues. AVAILABILITY AND IMPLEMENTATION: https://github.com/kuanglab/GraphTucker.

Indexed as

AlgorithmsTranscriptomeComputational BiologyGene Expression ProfilingHumans

Identifiers

PMID38940176
PMCPMC11256919

What OpenQuestion holds

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LicenceCC BY
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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.