Evidence map›Paper›PMID 41397970›Full record

ArticleNature communications2025

Accurate imputation of pathway-specific gene expression in spatial transcriptomics with PASTA.

Ruoxing Li, Peng Yang, Mauro Di Pilato, Jianjun Zhang, Christopher R Flowers, Lulu Shang, Ziyi Li

Abstract read
In one paragraph

Article in Nature communications, 2025. 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. Article
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  3. Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Ruoxing LiDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0003-4258-6321
Peng YangDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0002-0630-9506
Mauro Di PilatoDepartment of Immunology, The Unviersity of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0003-3902-7406
Jianjun ZhangDepartment of Thoracic/Head and Neck Medical Oncology, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0001-7872-3477
Christopher R FlowersDepartment of Lymphoma - Myeloma, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Lulu ShangDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. LShang@mdanderson.org.ORCID http://orcid.org/0000-0002-2480-3065
Ziyi LiDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. Zli16@mdanderson.org.ORCID http://orcid.org/0000-0001-8359-0533

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
UNIVERSITY OF TEXAS--SPORE IN LUNG CANCERP50CA070907 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI GIBBONS, DON LYNN · 1996 to 2024
$57.4M
The University of Texas MD Anderson Cancer Center SPORE in MelanomaP50CA221703 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DAVIES, MICHAEL · 2019 to 2023
$10.3M
Coordinating and Data Management Center for Translational and Basic Science Research in Early LesionsU24CA274212 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Liang Li, Ying Yuan · 2022 to 2026
$3.5M
Statistical methods to delineate the spatial and temporal pattern of cell-cell interactions in Spatial Transcriptomics dataR35GM159819 · NIGMS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Ziyi Li · 2025 to 2026
$899k
NCI NIH HHS P30 CA008748NCI NIH HHS P50 CA070907NCI NIH HHS P50 CA221703NCI NIH HHS U24 CA274212NIGMS NIH HHS R35 GM159819
6 · The paper itself

Abstract

Mapping the entire transcriptome at single-cell resolution under its natural spatial context is essential for investigating the oncogenesis and progression of diseases. The recently emerged targeted in-situ technologies retain the spatial organization of cells at high resolution, although they remain limited in the number of genes that can be simultaneously measured. To overcome this obstacle, numerous computational methods have been developed to predict unmeasured gene expression in spatial transcriptomics data by leveraging scRNA-seq data. Most of these methods focus on the expression of individual genes and usually generate highly variable predictions. In this study, we introduce PASTA (PAthway-oriented Spatial gene impuTAtion), a spatial pathway expression imputation method that leverages cell type and spatial proximity to enhance prediction accuracy. PASTA assumes that nearby cells and cells of the same type exhibit similar expression patterns, along with pathway information integrated into the imputation process, which improves prediction robustness and enhances biological relevance in spatial transcriptomics data. We demonstrate PASTA's superior performance across both simulated and real-world datasets, highlighting its ability to impute pathway gene expression with improved stability and biological significance.

Indexed as

Computational BiologyGene Expression ProfilingSingle-Cell AnalysisTranscriptomeAlgorithmsHumansRNA-Seq

Identifiers

PMID41397970
PMCPMC12820036

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Registered trials

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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.