Evidence map›Paper›PMID 31883325›Full record

SynthesisBiostatistics (Oxford, England)2021

Trans-ethnic meta-analysis of rare variants in sequencing association studies.

Jingchunzi Shi, Michael Boehnke, Seunggeun Lee

Abstract readMeta-Analysis
In one paragraph

Synthesis in Biostatistics (Oxford, England), 2021. 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

3 authors.

Jingchunzi ShiThomas Francis, Jr. School of Public Health II, 1420 Washington Heights, Ann Arbor, MI 48109, USA.
Michael BoehnkeThomas Francis, Jr. School of Public Health II, 1420 Washington Heights, Ann Arbor, MI 48109, USA.
Seunggeun LeeThomas Francis, Jr. School of Public Health II, 1420 Washington Heights, Ann Arbor, MI 48109, USA.

Funding

Design and Analysis of Human Gene Mapping StudiesR01HG009976 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BOEHNKE, MICHAEL L · 2018 to 2022
$2.5M
Statistical and computational methods for rare variant association analysisR01HG008773 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MUKHERJEE, BHRAMAR · 2016 to 2020
$1.9M
NHGRI NIH HHS R01 HG008773NHGRI NIH HHS R01 HG009976
6 · The paper itself

Abstract

Trans-ethnic meta-analysis is a powerful tool for detecting novel loci in genetic association studies. However, in the presence of heterogeneity among different populations, existing gene-/region-based rare variants meta-analysis methods may be unsatisfactory because they do not consider genetic similarity or dissimilarity among different populations. In response, we propose a score test under the modified random effects model for gene-/region-based rare variants associations. We adapt the kernel regression framework to construct the model and incorporate genetic similarities across populations into modeling the heterogeneity structure of the genetic effect coefficients. We use a resampling-based copula method to approximate asymptotic distribution of the test statistic, enabling efficient estimation of p-values. Simulation studies show that our proposed method controls type I error rates and increases power over existing approaches in the presence of heterogeneity. We illustrate our method by analyzing T2D-GENES consortium exome sequence data to explore rare variant associations with several traits.

Indexed as

Genome-Wide Association StudyModels, GeneticComputer SimulationGenetic Association StudiesGenetic VariationHumansPhenotypeEffect-size heterogeneitygenome-wide association studyKernel regressionRandom effect modelRare variantsTrans-ethnic meta-analysis

Identifiers

PMID31883325
PMCPMC8511946

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.