Evidence map›Paper›PMID 27857226›Full record

ArticleScientific reports2016

A Nonparametric Regression Approach to Control for Population Stratification in Rare Variant Association Studies.

Qiuying Sha, Kui Zhang, Shuanglin Zhang

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

3 authors.

Qiuying ShaDepartment of Mathematical Sciences, Michigan Technological University, Houghton, MI 49931, USA.
Kui ZhangDepartment of Mathematical Sciences, Michigan Technological University, Houghton, MI 49931, USA.
Shuanglin ZhangDepartment of Mathematical Sciences, Michigan Technological University, Houghton, MI 49931, USA.

Funding

GENETIC ANALYSIS OF COMMON DISEASES: AN EVALUATIONR01GM031575 · NIGMS · UNIVERSITY OF TEXAS RIO GRANDE VALLEY · PI ALMASY, LAURA A. · 1985 to 2016
$7.8M
Next-Generation Bioinformatics for Next-Generation SequencingR01HG008115 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI YU, FULI, ZHANG, KUI · 2014 to 2016
$1.4M
Statistical Methods for Rare Variant Association StudiesR15HG008209 · NHGRI · MICHIGAN TECHNOLOGICAL UNIVERSITY · PI SHA, QIUYING · 2016 to 2016
$437k
QUANTITATIVE TRAIT LOCUS MAPPING IN HUMAN PEDIGREESR01MH059490 · NIMH · SOUTHWEST FOUNDATION FOR BIOMEDICAL RES · PI BLANGERO, JOHN · 1998 to 2000
$426k
NHGRI NIH HHS R01 HG008115NHGRI NIH HHS R15 HG008209NIGMS NIH HHS R01 GM031575NIMH NIH HHS R01 MH059490
6 · The paper itself

Abstract

Recently, there is increasing interest to detect associations between rare variants and complex traits. Rare variant association studies usually need large sample sizes due to the rarity of the variants, and large sample sizes typically require combining information from different geographic locations within and across countries. Although several statistical methods have been developed to control for population stratification in common variant association studies, these methods are not necessarily controlling for population stratification in rare variant association studies. Thus, new statistical methods that can control for population stratification in rare variant association studies are needed. In this article, we propose a principal component based nonparametric regression (PC-nonp) approach to control for population stratification in rare variant association studies. Our simulations show that the proposed PC-nonp can control for population stratification well in all scenarios, while existing methods cannot control for population stratification at least in some scenarios. Simulations also show that PC-nonp's robustness to population stratification will not reduce power. Furthermore, we illustrate our proposed method by using whole genome sequencing data from genetic analysis workshop 18 (GAW18).

Indexed as

Genetic Predisposition to DiseaseModels, GeneticComputer SimulationGenetic Association StudiesGenetics, PopulationGenotypeHumansPhenotypePolymorphism, Single Nucleotide

Identifiers

PMID27857226
PMCPMC5114546

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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.