Evidence map›Paper›PMID 35205424›Full record

ArticleGenes2022

Leveraging Gene-Level Prediction as Informative Covariate in Hypothesis Weighting Improves Power for Rare Variant Association Studies.

Ying Ji, Rui Chen, Quan Wang, Qiang Wei, Ran Tao, Bingshan Li

Abstract read
In one paragraph

Article in Genes, 2022. 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
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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

6 authors.

Ying JiDepartment of Molecular Physiology & Biophysics, Vanderbilt University, Nashville, TN 37232, USA.
Rui ChenDepartment of Molecular Physiology & Biophysics, Vanderbilt University, Nashville, TN 37232, USA.
Quan WangDepartment of Molecular Physiology & Biophysics, Vanderbilt University, Nashville, TN 37232, USA.
Qiang WeiDepartment of Molecular Physiology & Biophysics, Vanderbilt University, Nashville, TN 37232, USA.
Ran TaoDepartment of Molecular Physiology & Biophysics, Vanderbilt University, Nashville, TN 37232, USA.
Bingshan LiDepartment of Molecular Physiology & Biophysics, Vanderbilt University, Nashville, TN 37232, USA.

Funding

Polygenic Risk Scores for Diverse Populations - Bridging Research and Clinical CareR01HL151152 · NHLBI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Christy Leigh Avery, Jennifer Below · 2020 to 2026
$12.3M
Analysis, Validation and Resource Creation for Genome Sequencing of Complex DiseasesU01HG009086 · NHGRI · VANDERBILT UNIVERSITY · PI COX, NANCY J, LI, BINGSHAN · 2016 to 2020
$4.3M
NHGRI NIH HHS U01 HG009086NHLBI NIH HHS R01 HL151152
6 · The paper itself

Abstract

Gene-based rare variant association studies (RVASs) have low power due to the infrequency of rare variants and the large multiple testing burden. To correct for multiple testing, traditional false discovery rate (FDR) procedures which depend solely on P-values are often used. Recently, Independent Hypothesis Weighting (IHW) was developed to improve the detection power while maintaining FDR control by leveraging prior information for each hypothesis. Here, we present a framework to increase power of gene-based RVASs by incorporating prior information using IHW. We first build supervised machine learning models to assign each gene a prediction score that measures its disease risk, using the input of multiple biological features, fed with high-confidence risk genes and local background genes selected near GWAS significant loci as the training set. Then we use the prediction scores as covariates to prioritize RVAS results via IHW. We demonstrate the effectiveness of this framework through applications to RVASs in schizophrenia and autism spectrum disorder. We found sizeable improvements in the number of significant associations compared to traditional FDR approaches, and independent evidence supporting the relevance of the genes identified by our framework but not traditional FDR, demonstrating the potential of our framework to improve power of gene-based RVASs.

Indexed as

Autism Spectrum DisorderSchizophreniaHumansfalse discovery rategene prioritizationGWASmachine learningmultiple hypothesis testingneuropsychiatric disordersrare variant association study

Identifiers

PMID35205424
PMCPMC8872452

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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.