Evidence map›Paper›PMID 28993617›Full record

ArticleScientific reports2017

A Bivariate Hypothesis Testing Approach for Mapping the Trait-Influential Gene.

Garrett Saunders, Guifang Fu, John R Stevens

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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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

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Garrett SaundersDepartment of Mathematics, Brigham Young University-Idaho, Rexburg, ID, 83460, USA.
Guifang FuDepartment of Mathematics and Statistics, Utah State University, Logan, UT, 84322, USA. Guifang.fu@usu.edu.
John R StevensDepartment of Mathematics and Statistics, Utah State University, Logan, UT, 84322, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The linkage disequilibrium (LD) based quantitative trait loci (QTL) model involves two indispensable hypothesis tests: the test of whether or not a QTL exists, and the test of the LD strength between the QTaL and the observed marker. The advantage of this two-test framework is to test whether there is an influential QTL around the observed marker instead of just having a QTL by random chance. There exist unsolved, open statistical questions about the inaccurate asymptotic distributions of the test statistics. We propose a bivariate null kernel (BNK) hypothesis testing method, which characterizes the joint distribution of the two test statistics in two-dimensional space. The power of this BNK approach is verified by three different simulation designs and one whole genome dataset. It solves a few challenging open statistical questions, closely separates the confounding between 'linkage' and 'QTL effect', makes a fine genome division, provides a comprehensive understanding of the entire genome, overcomes limitations of traditional QTL approaches, and connects traditional QTL mapping with the newest genotyping technologies. The proposed approach contributes to both the genetics literature and the statistics literature, and has a potential to be extended to broader fields where a bivariate test is needed.

Indexed as

Chromosome MappingModels, GeneticComputer SimulationData AnalysisGenome-Wide Association StudyLinkage DisequilibriumQuantitative Trait Loci

Identifiers

PMID28993617
PMCPMC5634470

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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.