Evidence map›Paper›PMID 38898015›Full record

ArticleNature communications2024

A robust model for cell type-specific interindividual variation in single-cell RNA sequencing data.

Minhui Chen, Andy Dahl

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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  5. Commentary: Lactylation-related geneFrontiers in immunology · 2025
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Minhui ChenSection of Genetic Medicine, University of Chicago, Chicago, IL, 60637, USA. minhuic@uchicago.edu.ORCID http://orcid.org/0000-0001-5684-2504
Andy DahlSection of Genetic Medicine, University of Chicago, Chicago, IL, 60637, USA. andywdahl@uchicago.edu.ORCID http://orcid.org/0000-0001-6520-4766

Funding

The Institute for Translational MedicineUL1TR002389 · NCATS · UNIVERSITY OF CHICAGO · PI Joshua J Jacobs, DAVID O MELTZER · 2017 to 2026
$71.6M
Novel statistical genetics methods to unravel polygenic interactions in complex traitsR35GM150822 · NIGMS · UNIVERSITY OF CHICAGO · PI Andrew Dahl · 2023 to 2026
$1.6M
Characterizing individual- and subtype-specific risk factors and treatments in asthmaK25HL157603 · NHLBI · UNIVERSITY OF CHICAGO · PI DAHL, ANDREW · 2021 to 2023
$519k
NCATS NIH HHS UL1 TR002389NHLBI NIH HHS K25 HL157603NIGMS NIH HHS R35 GM150822U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) K25HL157603
6 · The paper itself

Abstract

Single-cell RNA sequencing (scRNA-seq) has been widely used to characterize cell types based on their average gene expression profiles. However, most studies do not consider cell type-specific variation across donors. Modelling this cell type-specific inter-individual variation could help elucidate cell type-specific biology and inform genes and cell types underlying complex traits. We therefore develop a new model to detect and quantify cell type-specific variation across individuals called CTMM (Cell Type-specific linear Mixed Model). We use extensive simulations to show that CTMM is powerful and unbiased in realistic settings. We also derive calibrated tests for cell type-specific interindividual variation, which is challenging given the modest sample sizes in scRNA-seq. We apply CTMM to scRNA-seq data from human induced pluripotent stem cells to characterize the transcriptomic variation across donors as cells differentiate into endoderm. We find that almost 100% of transcriptome-wide variability between donors is differentiation stage-specific. CTMM also identifies individual genes with statistically significant stage-specific variability across samples, including 85 genes that do not have significant stage-specific mean expression. Finally, we extend CTMM to partition interindividual covariance between stages, which recapitulates the overall differentiation trajectory. Overall, CTMM is a powerful tool to illuminate cell type-specific biology in scRNA-seq.

Indexed as

Cell DifferentiationInduced Pluripotent Stem CellsSequence Analysis, RNASingle-Cell AnalysisTranscriptomeEndodermGene Expression ProfilingHumansRNA-Seq

Identifiers

PMID38898015
PMCPMC11186839

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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.