Evidence map›Paper›PMID 41256660›Full record

ArticlebioRxiv : the preprint server for biology2025

scGPD: single-cell informed gene panel design for targeted spatial transcriptomics.

Yunshan Guo, Jia Zhao, Rui B Chang, Hongyu Zhao

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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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0citing papers 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

The trial behind it

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3 · Its place in the literature

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Yunshan GuoDepartment of Biostatistics, School of Public Health, Yale University, New Haven, CT, USA.
Jia ZhaoDepartment of Biostatistics, School of Public Health, Yale University, New Haven, CT, USA.ORCID 0000-0002-9107-8852
Rui B ChangDepartment of Neuroscience, School of Medicine, Yale University, New Haven, CT, USA.
Hongyu ZhaoDepartment of Biostatistics, School of Public Health, Yale University, New Haven, CT, USA.ORCID 0000-0003-1195-9607

Funding

Laboratory, Data Analysis, and Coordinating Center (LDACC) for the Developmental Human Genotype-Tissue Expression ProjectU24HG012108 · NHGRI · YALE UNIVERSITY · PI GERSTEIN, MARK BENDER, HUTTNER, ANITA JULIANE · 2021 to 2025
$8.7M
Computational and Statistical Methods to determine variant effect across cell types and development stagesU01HG013840 · NHGRI · YALE UNIVERSITY · PI GERSTEIN, MARK BENDER, ZHAO, HONGYU · 2024 to 2024
$1.9M
NHGRI NIH HHS U01 HG013840NHGRI NIH HHS U24 HG012108
6 · The paper itself

Abstract

In targeted spatial transcriptomics technologies, a key challenge is to select an informative gene panel that captures the complexity of cellular and spatial heterogeneity within tissues. Many existing methods use prior knowledge or heuristic selection rules, such as selecting highly variable genes, which overlook gene-gene correlations and may consequently result in suboptimal coverage. To address the limitations of the existing methods, we introduce scGPD, a deep learning-based framework for gene panel design that leverages single-cell RNA-seq data to identify compact, nonredundant sets of genes for spatial profiling. scGPD uses a gene-gene correlation-aware gating mechanism to extract informative features from data, encouraging diversity among selected genes and eliminating redundancy. Across diverse single-cell datasets, scGPD outperforms existing gene panel design methods in recovering transcriptome-wide expression using a limited number of genes. When applied to spatial transcriptomics data, it achieves superior cell type classification accuracy, demonstrating strong generalization across modalities. The gene panels selected by scGPD further exhibit well-defined spatial expression patterns, highlighting their robustness and relevance for spatial analysis. The scGPD framework is flexible and can be adapted to multiple use cases, enabling the prioritization of genes relevant to specific diseases or phenotypes. Together, these results demonstrate that scGPD provides a robust and adaptable solution to design efficient gene panels for spatial transcriptomics, with broad applicability to tissue mapping and disease characterization.

Identifiers

PMID41256660
PMCPMC12621718

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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.