Evidence map›Paper›PMID 41633767›Full record

ArticleGenome research2026

spRefine denoises and imputes spatial transcriptomic data with a reference-free framework powered by genomic language model.

Tianyu Liu, Tinglin Huang, Wengong Jin, Tinyi Chu, Rex Ying, Hongyu Zhao

Abstract read
In one paragraph

Article in Genome research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. SpaGene: A Deep Adversarial Framework for Spatial Gene Imputation.Computational and structural biotechnology journal · 2026
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Tianyu LiuInterdepartmental Program in Computational Biology & Bioinformatics, Yale University, New Haven, Connecticut 06511, USA.
Tinglin HuangDepartment of Computer Science, Yale University, New Haven, Connecticut 06511, USA.
Wengong JinDepartment of Computer Science, Northeastern University, Boston, Massachusetts 02115, USA.
Tinyi ChuDepartment of Biostatistics, Yale University, New Haven, Connecticut 06511, USA.
Rex YingDepartment of Computer Science, Yale University, New Haven, Connecticut 06511, USA.
Hongyu ZhaoInterdepartmental Program in Computational Biology & Bioinformatics, Yale University, New Haven, Connecticut 06511, USA; hongyu.zhao@yale.edu.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
Computational Modeling of the Interplay between External Signaling and Transcription Rewiring using Spatial Transcriptomics and Single Cell Multiome DataK99HG013429 · NHGRI · YALE UNIVERSITY · PI CHU, TIN YI · 2024 to 2025
$284k
NHGRI NIH HHS K99 HG013429NHGRI NIH HHS U01 HG013840NHGRI NIH HHS U24 HG012108
6 · The paper itself

Abstract

The analysis of spatial transcriptomic data is hindered by high noise levels and missing gene measurements, challenges that are further compounded by the higher cost of spatial data compared to traditional single-cell data. To overcome this challenge, we introduce spRefine, a deep learning framework that leverages genomic language models to jointly denoise and impute spatial transcriptomic data. Our results demonstrate that spRefine yields more robust cell- and spot-level representations after denoising and imputation, substantially improving data integration. In addition, spRefine serves as a strong framework for model pretraining and the discovery of novel biological signals, as highlighted by multiple downstream applications across data sets of varying scales. Notably, spRefine enhances the accuracy of spatial aging clock estimations and uncovers new aging-related relationships associated with key biological processes, such as neuronal function loss, which offers new insights for analyzing aging effect with spatial transcriptomics.

Indexed as

Deep LearningGenomicsTranscriptomeAgingAnimalsGene Expression ProfilingHumansSpatial Transcriptomics

Identifiers

PMID41633767
PMCPMC13138011

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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.