Evidence map›Paper›PMID 33161601›Full record

ArticleGenetic epidemiology2021

Novel score test to increase power in association test by integrating external controls.

Yatong Li, Seunggeun Lee

Abstract read
In one paragraph

Article in Genetic epidemiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
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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

2 authors.

Yatong LiDepartment of Biostatistics, University of Michigan, Ann Arbor, Michigan, USA.
Seunggeun LeeDepartment of Biostatistics, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0000-0002-8097-3878

Funding

University of Michigan Training Program in Genomic ScienceT32HG000040 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Sebastian Zoellner · 1995 to 2026
$16.4M
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 T32 HG000040NIH HHS R01-HG008773
6 · The paper itself

Abstract

Recent advances in genotyping and sequencing technologies have enabled genetic association studies to leverage high-quality genotyped data to identify variants accounting for a substantial portion of disease risk. The usage of external controls, whose genomes have already been genotyped and are publicly available, could be a cost-effective approach to increase the power of association testing. There has been recent effort to integrate external controls while adjusting for possible batch effects, such as the integrating External Controls into Association Test (iECAT). The original iECAT test, however, cannot adjust for covariates such as age, gender, and so forth. Hence, based on the insight of iECAT, we propose a novel score-based test that allows for covariate adjustment and constructs a shrinkage score statistic that is a weighted sum of the score statistics using exclusively internal samples and uses both internal and external control samples. We assess the existence of batch effect at a variant by comparing control samples of internal and external sources. We show by simulation studies that our method has increased power over the original iECAT while controlling for type I error rates. We present the application of our method to the association studies of age-related macular degeneration (AMD) utilizing data from the International AMD Genomics Consortium and Michigan Genomics Initiative. Through the incorporation of the score test approach, we extend the use of iECAT to adjust for covariates and improve power, further honing the statistical methods needed to identify disease-causing variants within the human genome.

Indexed as

Macular DegenerationPolymorphism, Single NucleotideGenetic Association StudiesGenotypeHumansModels, Geneticcase-control studyexternal controlsGWASsaddlepoint approximation

Identifiers

PMID33161601
PMCPMC9424128

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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.