Evidence map›Paper›PMID 41469386›Full record

ArticleNature communications2025

CellScope: high-performance cell atlas workflow with tree-structured representation.

Bingjie Li, Runyu Lin, Tianhao Ni, Guanao Yan, Mannix Burns, Jingyi Jessica Li, Zhigang Yao

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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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.

Bingjie Li *Department of Statistics and Data Science, National University of Singapore, Singapore, Singapore.
Runyu Lin *Department of Statistics and Data Science, National University of Singapore, Singapore, Singapore.
Tianhao Ni *Department of Statistics and Data Science, National University of Singapore, Singapore, Singapore.
Guanao YanDepartment of Statistics, University of California, Los Angeles, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0002-6861-1882
Mannix BurnsDepartment of Molecular, Cell and Developmental Biology, University of California, Los Angeles, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0001-6091-3010
Jingyi Jessica LiBiostatistics Program, Public Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, WA, USA. lijy03@fredhutch.org.ORCID http://orcid.org/0000-0002-9288-5648
Zhigang YaoDepartment of Statistics and Data Science, National University of Singapore, Singapore, Singapore. zhigang.yao@nus.edu.sg.ORCID http://orcid.org/0000-0001-5927-6958

Funding

Ministry of Education - Singapore (MOE) A-0008520-00-00Ministry of Education - Singapore (MOE) A-8001562-00-00Ministry of Education - Singapore (MOE) A-8002931-00-00
6 · The paper itself

Abstract

Single-cell sequencing enables comprehensive profiling of individual cells, revealing cellular heterogeneity and function with unprecedented resolution. However, current analysis frameworks lack the ability to simultaneously explore and visualize cellular hierarchies at multiple biological levels. To address these limitations, we present CellScope, a promising framework for constructing high-resolution cell atlases at multiple clustering levels. CellScope employs a two-stage manifold fitting process for gene selection and noise reduction, followed by agglomerative clustering, and integrates UMAP visualization with hierarchical clustering to intuitively represent cellular relationships simultaneously at multiple levels-such as cell lineage, cell type, and cell subtype levels. Compared to established pipelines such as Seurat and Scanpy, CellScope comprehensively improves clustering performance, visualization clarity, computational efficiency, and algorithm interpretability, while reducing dependence on hyperparameters across a multitude of single-cell datasets. Most importantly, it can reveal biological insights that other contemporary methods are unable to detect, thereby deepening our understanding of cellular heterogeneity and function, and potentially informing disease research.

Indexed as

Computational BiologySingle-Cell AnalysisSoftwareAlgorithmsAnimalsCell LineageCluster AnalysisGene Expression ProfilingHumansWorkflow

Identifiers

PMID41469386
PMCPMC12855844

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.