Evidence map›Paper›PMID 32270270›Full record

ArticleHuman genetics2020

Joint modeling of eQTLs and parent-of-origin effects using an orthogonal framework with RNA-seq data.

Shirong Deng, James Hardin, Christopher I Amos, Feifei Xiao

Abstract readEvaluation Study
PubMed Publisher
In one paragraph

Article in Human genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 51% of its field
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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Abundant Parent-of-origin Effect eQTL: The Framingham Heart Study.bioRxiv : the preprint server for biology · 2025
    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 at 3 institutions in 2 countries.

Shirong DengSchool of Mathematics and Statistics, Wuhan University, Wuhan, China.
James HardinDepartment of Epidemiology and Biostatistics, Arnold School of Public Health, University of South Carolina, Room 449, 915 Greene St., Columbia, SC, 29201, USA.
Christopher I AmosDepartment of Quantitative Sciences, Baylor College of Medicine, Houston, TX, 77030, USA.
Feifei XiaoDepartment of Epidemiology and Biostatistics, Arnold School of Public Health, University of South Carolina, Room 449, 915 Greene St., Columbia, SC, 29201, USA. xiaof@mailbox.sc.edu.ORCID http://orcid.org/0000-0002-1597-4719
University of South Carolina · USBaylor College of Medicine · USWuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extensive studies have been conducted on the analysis of genome function, especially on the expression quantitative trait loci (eQTL). These studies offered promising results for characterization of the functional sequencing variation and understanding of the basic processes of gene regulation. Parent of origin effect (POE) is an important epigenetic phenomenon describing that the expression of certain genes depends on their allelic parent-of-origin and it is known to play important roles in human complex diseases. However, traditional eQTL mapping approaches do not allow for the detection of imprinting, or they focus on modeling the additive genetic effect thereby ignoring the estimation of the dominance genetic effect. In this study, we proposed a statistical framework to test the additive and dominance genetic effects of the candidate eQTLs along with detection of the POE with a functional model and an orthogonal model for RNA-seq data. We demonstrated the desirable power and preserved Type I errors of the methods in most scenarios, especially the orthogonal model with un-biased estimation of the genetic effects and over-dispersion of the RNA-seq data. The application to a HapMap project trio dataset validated existing imprinting genes and discovered two novel imprinting genes with potential dominance genetic effect and RB1 and IGF1R genes. This study provides new insights into the next generation statistical modeling of eQTL mapping for better understanding of the genetic architecture underlying the mechanisms of gene expression regulation.

Indexed as

Models, GeneticModels, StatisticalAllelesChildComputer SimulationFamilyFemaleGene Expression RegulationGenes, DominantGenomic ImprintingGenotypeHapMap ProjectHumansMaleParentsPolymorphism, Single Nucleotide

Identifiers

PMID32270270
OpenAlexW3015791675

What OpenQuestion holds

Textmetadata
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.