Evidence map›Paper›PMID 35561178›Full record

ArticleBioinformatics (Oxford, England)2022

EDClust: an EM-MM hybrid method for cell clustering in multiple-subject single-cell RNA sequencing.

Xin Wei, Ziyi Li, Hongkai Ji, Hao Wu

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2022. 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

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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

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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

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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.

Xin WeiDepartment of Biostatistics and Bioinformatics, Emory University, Atlanta, GA 30322, USA.
Ziyi LiDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Hongkai JiDepartment of Biostatistics, Johns Hopkins University, Baltimore, MD 21205, USA.
Hao WuDepartment of Biostatistics and Bioinformatics, Emory University, Atlanta, GA 30322, USA.ORCID 0000-0003-1269-7354

Funding

Statistical Methods for Single-Cell RNA-SeqR01GM122083 · NIGMS · EMORY UNIVERSITY · PI WU, HAO · 2016 to 2020
$1.7M
Computational tools for regulome mapping using single-cell genomic dataR01HG010889 · NHGRI · JOHNS HOPKINS UNIVERSITY · PI JI, HONGKAI · 2019 to 2022
$1.6M
Statistical models for intratumor heterogeneity of tumor-infiltrated leukocytes in lung cancerR03CA270725 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LI, ZIYI · 2022 to 2023
$162k
NCI NIH HHS R03 CA270725NHGRI NIH HHS R01 HG010889NIGMS NIH HHS R01 GM122083NIH HHS R01GM122083
6 · The paper itself

Abstract

motivationSingle-cell RNA sequencing (scRNA-seq) has revolutionized biological research by enabling the measurement of transcriptomic profiles at the single-cell level. With the increasing application of scRNA-seq in larger-scale studies, the problem of appropriately clustering cells emerges when the scRNA-seq data are from multiple subjects. One challenge is the subject-specific variation; systematic heterogeneity from multiple subjects may have a significant impact on clustering accuracy. Existing methods seeking to address such effects suffer from several limitations.

resultsWe develop a novel statistical method, EDClust, for multi-subject scRNA-seq cell clustering. EDClust models the sequence read counts by a mixture of Dirichlet-multinomial distributions and explicitly accounts for cell-type heterogeneity, subject heterogeneity and clustering uncertainty. An EM-MM hybrid algorithm is derived for maximizing the data likelihood and clustering the cells. We perform a series of simulation studies to evaluate the proposed method and demonstrate the outstanding performance of EDClust. Comprehensive benchmarking on four real scRNA-seq datasets with various tissue types and species demonstrates the substantial accuracy improvement of EDClust compared to existing methods. AVAILABILITY AND IMPLEMENTATION: The R package is freely available at https://github.com/weix21/EDClust. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

Gene Expression ProfilingSingle-Cell AnalysisAlgorithmsCluster AnalysisHumansSequence Analysis, RNA

Identifiers

PMID35561178
PMCPMC9113373

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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.