Evidence map›Paper›PMID 41996577›Full record

ArticleBriefings in bioinformatics2026

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

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

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 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

4 authors.

Yunshan GuoDepartment of Biostatistics, School of Public Health, Yale University, 300 George Street, Ste 503, New Haven, CT 06511, United States.ORCID 0009-0008-8246-1359
Jia ZhaoDepartment of Biostatistics, School of Public Health, Yale University, 300 George Street, Ste 503, New Haven, CT 06511, United States.
Rui B ChangDepartment of Neuroscience, School of Medicine, Yale University, 200 S Frontage Rd, New Haven, CT 06510, United States.
Hongyu ZhaoDepartment of Biostatistics, School of Public Health, Yale University, 300 George Street, Ste 503, New Haven, CT 06511, United States.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 HG012108NIH HHS U01 HG013840NIH 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 single-cell informed Gene Panel Design (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 competitive and robust cell-type classification performance, 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.

Indexed as

Deep LearningGene Expression ProfilingSingle-Cell AnalysisTranscriptomeAnimalsHumansSingle-Cell Gene Expression AnalysisSpatial Transcriptomicsdeep learninggene panel designspatial transcriptomics

Identifiers

PMID41996577
PMCPMC13089504

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.