Evidence map›Paper›PMID 39788105›Full record

ArticleCell genomics2025

CSI-GEP: A GPU-based unsupervised machine learning approach for recovering gene expression programs in atlas-scale single-cell RNA-seq data.

Xueying Liu, Richard H Chapple, Declan Bennett, William C Wright, Ankita Sanjali, Erielle Culp, Yinwen Zhang, Min Pan, Paul Geeleher

Abstract read
In one paragraph

Article in Cell genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

9 authors.

Xueying LiuDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Richard H ChappleDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Declan BennettDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
William C WrightDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Ankita SanjaliDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Erielle CulpDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA; Department of Genetics, Genomics, and Informatics, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Yinwen ZhangDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Min PanDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Paul GeeleherDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA. Electronic address: paul.geeleher@stjude.org.

Funding

Developing new therapeutic strategies for pediatric tumors that lack clinically actionable mutationsR01CA260060 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Paul Geeleher · 2021 to 2026
$3.0M
Computational tools for estimating cell-type-specific effects in bulk RNA-seq and spatial transcriptomics data, using reference single-cell RNA-seq datasetsR35GM138293 · NIGMS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI GEELEHER, PAUL · 2020 to 2024
$2.2M
Novel computational approaches for pharmacogenomic discoveryR00HG009679 · NHGRI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI GEELEHER, PAUL · 2019 to 2021
$739k
NCI NIH HHS R01 CA260060NHGRI NIH HHS R00 HG009679NIGMS NIH HHS R35 GM138293
6 · The paper itself

Abstract

Exploratory analysis of single-cell RNA sequencing (scRNA-seq) typically relies on hard clustering over two-dimensional projections like uniform manifold approximation and projection (UMAP). However, such methods can severely distort the data and have many arbitrary parameter choices. Methods that can model scRNA-seq data as non-discrete "gene expression programs" (GEPs) can better preserve the data's structure, but currently, they are often not scalable, not consistent across repeated runs, and lack an established method for choosing key parameters. Here, we developed a GPU-based unsupervised learning approach, "consensus and scalable inference of gene expression programs" (CSI-GEP). We show that CSI-GEP can recover ground truth GEPs in real and simulated atlas-scale scRNA-seq datasets, significantly outperforming cutting-edge methods, including GPT-based neural networks. We applied CSI-GEP to a whole mouse brain atlas of 2.2 million cells, disentangling endothelial cell types missed by other methods, and to an integrated scRNA-seq atlas of human tumors and cell lines, discovering mesenchymal-like GEPs unique to cancer cells growing in culture.

Indexed as

RNA-SeqSingle-Cell AnalysisUnsupervised Machine LearningAnimalsBrainGene Expression ProfilingHumansMiceSequence Analysis, RNASingle-Cell Gene Expression Analysissingle-cell genomicssingle-cell RNA-sequnsupervised machine learning

Identifiers

PMID39788105
PMCPMC11770216

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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.