Evidence map›Paper›PMID 41920506›Full record

ArticleInterdisciplinary sciences, computational life sciences2026

KGLAR: Deconvoluting Spatial Transcriptomics Data with Single-cell Transcriptomes through Knowledge-guided NMF and Least Angle Regression.

Lihong Peng, Feixiang Wang, Wei Wu, Xinhuai Peng, Wei Xiong, Yan Jiang, Libo Nie, Xing Chen

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

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Lihong Peng *School of Computer, Hunan University of Technology, Zhuzhou, 412007, China.ORCID http://orcid.org/0000-0002-2321-3901
Feixiang Wang *School of Computer, Hunan University of Technology, Zhuzhou, 412007, China.
Wei WuSchool of Biological Science and Medical Engineering, Hunan University of Technology, Zhuzhou, 412007, China.
Xinhuai PengSchool of Computer, Hunan University of Technology, Zhuzhou, 412007, China.
Wei XiongSchool of Computer, Hunan University of Technology, Zhuzhou, 412007, China.
Yan JiangSchool of Information Engineering, Changsha Medical University, Changsha, 410219, China.
Libo NieSchool of Biological Science and Medical Engineering, Hunan University of Technology, Zhuzhou, 412007, China. nielibo@hut.edu.cn.
Xing ChenSchool of Science, Jiangnan University, Wuxi, 214122, China. xingchen@amss.ac.cn.

Funding

National Natural Science Foundation of China 61803151National Natural Science Foundation of China 92370131Natural Science Foundation of Hunan Province 2023JJ50201Natural Science Foundation of Hunan Province 2024JJ7133
6 · The paper itself

Abstract

The advance in spatial transcriptomics (ST) technologies has brought great opportunities to unlock cellular heterogeneity in cancers. However, most of current spatially resolved transcriptomic technologies provide the mean gene expression of spots and do not still have single-cell resolution in breadth and depth. The deconvolution technique can efficiently integrate gene expression and spatial location to annotate cell types. Here, we report KGLAR, a novel deconvolution framework for cell type annotation by integrating single-cell RNA sequencing and ST data. KGLAR incorporates topic identification through knowledge-guided non-negative matrix factorization, topic distribution analysis with least angle regression, cell type annotation based on non-negative least squares, and label refinement by combining spatial information. Using 4 different evaluation metrics, KGLAR is compared with other 10 state-of-the-art deconvolution methods on 2 gridded and 17 pseudo-ST datasets. KGLAR surpassed the 10 cell-type deconvolution methods under different sequencing depths, different sequencing platforms and different tissues within a relatively short period of time. Furthermore, KGLAR is capable of precisely mapping subtle cortical layers and the hippocampus architectures in mouse brain, and accurately annotating tumor-specific immune cell types with different spatial distributions in the pancreatic ductal adenocarcinoma tissue. KGLAR provides a publicly available R package and facilitates to dissect spatial and cellular heterogeneity.

Indexed as

DeconvolutionLeast angle regressionNon-negative least squaresNon-negative matrix factorizationSingle-cell RNA sequencingSpatial transcriptomics

Identifiers

PMID41920506

What OpenQuestion holds

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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.