Evidence map›Paper›PMID 40093202›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Efficient count-based models improve power and robustness for large-scale single-cell eQTL mapping.

Zixuan Eleanor Zhang, Artem Kim, Noah Suboc, Nicholas Mancuso, Steven Gazal

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. 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

5 authors.

Zixuan Eleanor ZhangCenter for Genetic Epidemiology, Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California.ORCID 0000-0001-7193-8694
Artem KimCenter for Genetic Epidemiology, Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California.ORCID 0000-0001-8824-2853
Noah SubocCenter for Genetic Epidemiology, Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California.
Nicholas MancusoCenter for Genetic Epidemiology, Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California.ORCID 0000-0002-9352-5927
Steven GazalCenter for Genetic Epidemiology, Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California.ORCID 0000-0003-4510-5730

Funding

Statistical Methods for Integrative Genomics in CancerP01CA196569 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI David V Conti · 2016 to 2026
$25.5M
Characterizing the evolutionary architecture of complex disease within and across diverse populationsR01HG012133 · NHGRI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MANCUSO, NICHOLAS · 2021 to 2025
$3.6M
Haplotype-aware models of gene and isoform expression with application to genetic studies of disease in diverse populationsR01GM140287 · NIGMS · SEATTLE CHILDREN'S HOSPITAL · PI GAMAZON, ERIC R, MOHAMMADI, PEJMAN · 2021 to 2024
$2.8M
An integrative multi-omics approach to characterize prostate cancer risk in diverse populationsR01CA258808 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Nicholas Mancuso · 2021 to 2026
$2.5M
Characterizing genetic signatures of natural selection to understand human diseasesR35GM147789 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Steven Gazal · 2022 to 2026
$2.0M
Computational Genomics Summer Institute and Mentoring NetworkR25GM135043 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ESKIN, ELEAZAR · 2020 to 2025
$1.6M
From common to rare variant functional architectures of human diseasesR00HG010160 · NHGRI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI GAZAL, STEVEN · 2020 to 2022
$727k
NCI NIH HHS P01 CA196569NCI NIH HHS R01 CA258808NHGRI NIH HHS R00 HG010160NHGRI NIH HHS R01 HG012133NIGMS NIH HHS R01 GM140287NIGMS NIH HHS R25 GM135043NIGMS NIH HHS R35 GM147789
6 · The paper itself

Abstract

Population-scale single-cell transcriptomic technologies (scRNA-seq) enable characterizing variant effects on gene regulation at the cellular level (e.g., single-cell eQTLs; sc-eQTLs). However, existing sc-eQTL mapping approaches are either not designed for analyzing sparse counts in scRNA-seq data or can become intractable in extremely large datasets. Here, we propose jaxQTL, a flexible and efficient sc-eQTL mapping framework using highly efficient count-based models given pseudobulk data. Using extensive simulations, we demonstrated that jaxQTL with a negative binomial model outperformed other models in identifying sc-eQTLs, while maintaining a calibrated type I error. We applied jaxQTL across 14 cell types of OneK1K scRNA-seq data (

Identifiers

PMID40093202
PMCPMC11908335

What OpenQuestion holds

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LicenceCC BY-NC
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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.