Evidence map›Paper›PMID 38809943›Full record

ArticlePLoS computational biology2024

Clustering and visualization of single-cell RNA-seq data using path metrics.

Andriana Manousidaki, Anna Little, Yuying Xie

Abstract read
In one paragraph

Article in PLoS computational biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Andriana ManousidakiDepartment of Statistics and Probability, Michigan State University, East Lansing, Michigan, United States of America.ORCID 0000-0001-9213-795X
Anna LittleDepartment of Mathematics, University of Utah, Salt Lake City, Utah, United States of America.
Yuying XieDepartment of Statistics and Probability, Michigan State University, East Lansing, Michigan, United States of America.ORCID 0000-0002-1049-2219

Funding

Restoring the Immunogenicity of Head and Neck CancerR01DE026728 · NIDCR · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Yu Leo Lei, James J. Moon · 2018 to 2026
$4.3M
Robust Immuno-prevention Strategies for High-Risk Oral Epithelial DysplasiaU01DE029255 · NIDCR · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BRENNER, JOHN CHADWICK, LEI, YU LEO · 2019 to 2021
$4.2M
Mathematical Model-Based Optimization of CRT Response in IschemiaR01HL166508 · NHLBI · CALIFORNIA MEDICAL INNOVATIONS INSTITUTE · PI GHASSAN S KASSAB, Lik Chuan Lee · 2023 to 2026
$3.1M
Advancing On-Slide and Optical Biopsy Tools to Detect High-Risk Oral PremalignancyU01DE033330 · NIDCR · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Steven Bennett Chinn, Yu Leo Lei · 2023 to 2026
$2.7M
Development of a Prognostic Compound Immunoscore for Head and Neck CancerR03DE027399 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LEI, YU LEO, XIE, YUYING · 2018 to 2019
$338k
NHLBI NIH HHS R01 HL166508NIDCR NIH HHS R01 DE026728NIDCR NIH HHS R03 DE027399NIDCR NIH HHS U01 DE029255NIDCR NIH HHS U01 DE033330
6 · The paper itself

Abstract

Recent advances in single-cell technologies have enabled high-resolution characterization of tissue and cancer compositions. Although numerous tools for dimension reduction and clustering are available for single-cell data analyses, these methods often fail to simultaneously preserve local cluster structure and global data geometry. To address these challenges, we developed a novel analyses framework, Single-Cell Path Metrics Profiling (scPMP), using power-weighted path metrics, which measure distances between cells in a data-driven way. Unlike Euclidean distance and other commonly used distance metrics, path metrics are density sensitive and respect the underlying data geometry. By combining path metrics with multidimensional scaling, a low dimensional embedding of the data is obtained which preserves both the global data geometry and cluster structure. We evaluate the method both for clustering quality and geometric fidelity, and it outperforms current scRNAseq clustering algorithms on a wide range of benchmarking data sets.

Indexed as

AlgorithmsComputational BiologySingle-Cell AnalysisCluster AnalysisGene Expression ProfilingHumansRNA-SeqSequence Analysis, RNASingle-Cell Gene Expression Analysis

Identifiers

PMID38809943
PMCPMC11164391

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.