Evidence map›Paper›PMID 31368479›Full record

ArticleBioinformatics (Oxford, England)2020

Bayesian estimation of genetic regulatory effects in high-throughput reporter assays.

William H Majoros, Young-Sook Kim, Alejandro Barrera, Fan Li, Xingyan Wang, Sarah J Cunningham, Graham D Johnson, Cong Guo, William L Lowe, Denise M Scholtens and 3 more

Open access · greenAbstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2020. 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, top 90% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

13 authors at 3 institutions in 3 countries.

William H MajorosDuke Center for Statistical Genetics and Genomics, Duke University.
Young-Sook KimCenter for Genomic and Computational Biology, Duke University Medical School.
Alejandro BarreraCenter for Genomic and Computational Biology, Duke University Medical School.
Fan LiDepartment of Biostatistics, Yale University, New Haven, CT 06520.
Xingyan WangMasters Program in Biostatistics, Department of Biostatistics and Bioinformatics, Duke University Medical School, Durham, NC 27710.
Sarah J CunninghamUniversity Program in Genetics and Genomics, Duke University.
Graham D JohnsonCenter for Genomic and Computational Biology, Duke University Medical School.
Cong GuoUniversity Program in Genetics and Genomics, Duke University.
William L LoweDivision of Endocrinology Metabolism and Molecular Medicine, Northwestern University Feinberg School of Medicine, Chicago.
Denise M ScholtensDivision of Biostatistics, Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
M Geoffrey HayesDivision of Endocrinology Metabolism and Molecular Medicine, Northwestern University Feinberg School of Medicine, Chicago.
Timothy E ReddyDuke Center for Statistical Genetics and Genomics, Duke University.
Andrew S AllenDuke Center for Statistical Genetics and Genomics, Duke University.
Duke University · USNorthwestern University · USYale University · US

Funding

Genetics Training Grant-Year 26T32GM007754 · NIGMS · DUKE UNIVERSITY · PI HAASE, STEVEN B · 1985 to 2019
$8.3M
Decoding and Reprogramming the Corticosteroid Transcriptional Regulatory NetworkU01HG007900 · NHGRI · DUKE UNIVERSITY · PI REDDY, TIMOTHY E · 2015 to 2017
$5.9M
Regulatory Mechanisms of CD4+ T Cell DifferentiationUM1HG009428 · NHGRI · DUKE UNIVERSITY · PI CIOFANI, MARIA, CRAWFORD, GREGORY E · 2017 to 2021
$4.6M
Genetics and Genomics of Maternal Glycemia During PregnancyR01DK097534 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LOWE, WILLIAM L · 2013 to 2017
$2.1M
Genetics and Evolution of Fetal Human Fat Accretion During DevelopmentR01DK099820 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LOWE, WILLIAM L · 2013 to 2017
$2.0M
Functional characterization of regulatory variants associated with maternal hyperglycemiaF32DK115188 · NIDDK · DUKE UNIVERSITY · PI JOHNSON, GRAHAM · 2017 to 2019
$184k
NHGRI NIH HHS U01 HG007900NHGRI NIH HHS UM1 HG009428NIDDK NIH HHS F32 DK115188NIDDK NIH HHS R01 DK097534NIDDK NIH HHS R01 DK099820NIGMS NIH HHS T32 GM007754
6 · The paper itself

Abstract

motivationHigh-throughput reporter assays dramatically improve our ability to assign function to noncoding genetic variants, by measuring allelic effects on gene expression in the controlled setting of a reporter gene. Unlike genetic association tests, such assays are not confounded by linkage disequilibrium when loci are independently assayed. These methods can thus improve the identification of causal disease mutations. While work continues on improving experimental aspects of these assays, less effort has gone into developing methods for assessing the statistical significance of assay results, particularly in the case of rare variants captured from patient DNA.

resultsWe describe a Bayesian hierarchical model, called Bayesian Inference of Regulatory Differences, which integrates prior information and explicitly accounts for variability between experimental replicates. The model produces substantially more accurate predictions than existing methods when allele frequencies are low, which is of clear advantage in the search for disease-causing variants in DNA captured from patient cohorts. Using the model, we demonstrate a clear tradeoff between variant sequencing coverage and numbers of biological replicates, and we show that the use of additional biological replicates decreases variance in estimates of effect size, due to the properties of the Poisson-binomial distribution. We also provide a power and sample size calculator, which facilitates decision making in experimental design parameters. AVAILABILITY AND IMPLEMENTATION: The software is freely available from www.geneprediction.org/bird. The experimental design web tool can be accessed at http://67.159.92.22:8080. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

SoftwareAllelesBayes TheoremGene FrequencyHumansLinkage Disequilibrium

Identifiers

PMID31368479
PMCPMC7999138
OpenAlexW2966631770

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.