Evidence map›Paper›PMID 38422960›Full record

ArticleComputers in biology and medicine2024

Multiscale differential geometry learning of networks with applications to single-cell RNA sequencing data.

Hongsong Feng, Sean Cottrell, Yuta Hozumi, Guo-Wei Wei

Abstract read
In one paragraph

Article in Computers in biology and medicine, 2024. 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. Multiscale Cell-Cell Interactive Spatial Transcriptomics Analysis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  2. DeepAtlas: a tool for effective manifold learning.bioRxiv : the preprint server for biology · 2025
    Article
  3. Article
  4. Hodge Decomposition of Single-Cell RNA Velocity.Journal of chemical information and modeling · 2024
    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.

Hongsong FengDepartment of Mathematics, Michigan State University, East Lansing, MI 48824, USA.
Sean CottrellDepartment of Mathematics, Michigan State University, East Lansing, MI 48824, USA.
Yuta HozumiDepartment of Mathematics, Michigan State University, East Lansing, MI 48824, USA.
Guo-Wei WeiDepartment of Mathematics, Michigan State University, East Lansing, MI 48824, USA; Department of Electrical and Computer Engineering, Michigan State University, East Lansing, MI 48824, USA; Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, MI 48824, USA. Electronic address: weig@msu.edu.

Funding

AI-based platform for predicting emerging vaccine-escape variants and designing mutation-proof antibodiesR01AI164266 · NIAID · UNIVERSITY OF GEORGIA · PI Guowei Wei, YONG-HUI ZHENG · 2022 to 2026
$2.7M
Discovery-Driven Mathematics and Artificial Intelligence for Biosciences and Drug DiscoveryR35GM148196 · NIGMS · UNIVERSITY OF GEORGIA · PI Guowei Wei · 2023 to 2026
$1.5M
Synergistic integration of topology and machine learning for the predictions of protein-ligand binding affinities and mutation impactsR01GM126189 · NIGMS · MICHIGAN STATE UNIVERSITY · PI WEI, GUOWEI · 2018 to 2021
$1.4M
NIAID NIH HHS R01 AI164266NIGMS NIH HHS R01 GM126189NIGMS NIH HHS R35 GM148196
6 · The paper itself

Abstract

Single-cell RNA sequencing (scRNA-seq) has emerged as a transformative technology, offering unparalleled insights into the intricate landscape of cellular diversity and gene expression dynamics. scRNA-seq analysis represents a challenging and cutting-edge frontier within the field of biological research. Differential geometry serves as a powerful mathematical tool in various applications of scientific research. In this study, we introduce, for the first time, a multiscale differential geometry (MDG) strategy for addressing the challenges encountered in scRNA-seq data analysis. We assume that intrinsic properties of cells lie on a family of low-dimensional manifolds embedded in the high-dimensional space of scRNA-seq data. Multiscale cell-cell interactive manifolds are constructed to reveal complex relationships in the cell-cell network, where curvature-based features for cells can decipher the intricate structural and biological information. We showcase the utility of our novel approach by demonstrating its effectiveness in classifying cell types. This innovative application of differential geometry in scRNA-seq analysis opens new avenues for understanding the intricacies of biological networks and holds great potential for network analysis in other fields.

Indexed as

Data AnalysisGene Expression ProfilingCluster AnalysisSequence Analysis, RNACell interactive manifoldCell type classificationDimensionality reductionMachine learningMultiscale differential geometryscRNA-seq data

Identifiers

PMID38422960
PMCPMC10965033

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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.