Evidence map›Paper›PMID 40057378›Full record

ArticleNucleic acids research2025

stAI: a deep learning-based model for missing gene imputation and cell-type annotation of spatial transcriptomics.

Guangsheng Zou, Qunlun Shen, Limin Li, Shuqin Zhang

Abstract read
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Article in Nucleic acids research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

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0cells of the map it votes in
13citing 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

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3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Article
  2. Review
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  7. Article
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  9. Applications and development of in situ nucleic acid visualization techniques.Frontiers in bioengineering and biotechnology · 2026
    Review
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  11. Article
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Guangsheng ZouSchool of Mathematical Sciences, Fudan University, Shanghai 200433, China.
Qunlun ShenSchool of Mathematical Sciences, Fudan University, Shanghai 200433, China.
Limin LiSchool of Mathematics and Statistics, Xi'an Jiaotong University, Xi'an 710049, China.ORCID 0000-0003-3572-6832
Shuqin ZhangSchool of Mathematical Sciences, Fudan University, Shanghai 200433, China.ORCID 0000-0001-8223-844X

Funding

National Key Research and Development Program of China 2021YFC2701601National Natural Science Foundation of China 12222115Science and Technology Innovation Plan of Shanghai Science and Technology Commission 23JC1401000
6 · The paper itself

Abstract

Spatial transcriptomics technology has revolutionized our understanding of cellular systems by capturing RNA transcript levels in their original spatial context. Single-cell spatial transcriptomics (scST) offers single-cell resolution expression level and precise spatial information of RNA transcripts, while it has a limited capacity for simultaneously detecting a wide range of RNA transcripts, hindering its broader applications. Characterizing the whole transcriptome level and comprehensively annotating cell types represent two significant challenges in scST applications. Despite several proposed methods for one or both tasks, their performance remains inadequate. In this work, we introduce stAI, a deep learning-based model designed to address both missing gene imputation and cell-type annotation for scST data. stAI leverages a joint embedding for the scST and the reference scRNA-seq data with two separate encoder-decoder modules. Both the imputation and annotation are performed within the latent space in a supervised manner, utilizing scRNA-seq data to guide the processes. Experiments for datasets generated from diverse platforms with varying numbers of measured genes were conducted and compared with the updated methods. The results demonstrate that stAI can predict the unmeasured genes, especially the marker genes, with much higher accuracy, and annotate the cell types, including those of small size, with high precision.

Indexed as

Deep LearningGene Expression ProfilingMolecular Sequence AnnotationSingle-Cell AnalysisTranscriptomeAnimalsHumansRNA-SeqSequence Analysis, RNASoftware

Identifiers

PMID40057378
PMCPMC11890069

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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.