Evidence map›Paper›PMID 41105729›Full record

ArticlePLoS computational biology2025

Stabilized marker gene identification and functional annotation from single-cell transcriptomic data.

Sandesh Acharya, Pathum Kossinna, Qingrun Zhang, Jiami Guo

Abstract read
In one paragraph

Article in PLoS computational biology, 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. Review
  2. 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

4 authors.

Sandesh AcharyaDepartment of Cell Biology and Anatomy, University of Calgary, Calgary, Alberta, Canada.
Pathum KossinnaAlberta Children's Hospital Research Institute, University of Calgary, Calgary, Alberta, Canada.
Qingrun ZhangAlberta Children's Hospital Research Institute, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0003-2701-0711
Jiami GuoDepartment of Cell Biology and Anatomy, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0002-1031-8798

Funding

NSERC DiscoveryThe New York Stem Cell Foundation
6 · The paper itself

Abstract

With the rapid emergence of single-cell transcriptomics datasets, reproducible marker genes and functional annotation of cell type or state is becoming increasingly important. Conventional methods that rely on differential gene expression (DEG) analysis lack both consistency across datasets and functional annotations of selected markers. Here, we present scSCOPE, an R-based platform that utilizes stabilized LASSO (Least Absolute Shrinkage and Selection Operator) feature selection, bootstrapped co-expression networks, and pathway enrichments to identify reproducible and functionally relevant marker genes and associated pathways in scRNAseq datasets. Using 9 scRNAseq datasets from human and mouse immune cells generated by different sequencing technologies, we show that scSCOPE outperforms other conventional methods by automatically identifying cell type-specific marker genes and pathways with the highest consistency across all datasets. scSCOPE's gene co-expression and pathway analyses also provide in-depth molecular insights into the functionality of identified marker genes. We anticipate that scSCOPE will greatly improve cell type annotation and accelerate the design of experimental validation and functional investigations on cell heterogeneity.

Indexed as

Gene Expression ProfilingMolecular Sequence AnnotationSingle-Cell AnalysisTranscriptomeAnimalsComputational BiologyDatabases, GeneticGenetic MarkersHumansMiceSequence Analysis, RNAGenetic Markers

Identifiers

PMID41105729
PMCPMC12533881

What OpenQuestion holds

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LicenceCC BY
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.