Evidence map›Paper›PMID 31831092›Full record

ArticleGenetics research2019

A permutation method for detecting trend correlations in rare variant association studies.

Lifeng Liu, Pengfei Wang, Jingbo Meng, Lili Chen, Wensheng Zhu, Weijun Ma

Open access · goldAbstract read
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Article in Genetics research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 34% of its field
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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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 at 2 institutions in 1 country.

Lifeng LiuSchool of Mathematical Sciences, Heilongjiang University, Harbin150080, China.
Pengfei WangKey Laboratory for Applied Statistics of MOE, School of Mathematics and Statistics, Northeast Normal University, Changchun130024, China.
Jingbo MengKey Laboratory for Applied Statistics of MOE, School of Mathematics and Statistics, Northeast Normal University, Changchun130024, China.
Lili ChenSchool of Mathematical Sciences, Heilongjiang University, Harbin150080, China.
Wensheng ZhuKey Laboratory for Applied Statistics of MOE, School of Mathematics and Statistics, Northeast Normal University, Changchun130024, China.ORCID 0000-0002-0156-3222
Weijun MaSchool of Mathematical Sciences, Heilongjiang University, Harbin150080, China.
Heilongjiang University · CNNortheast Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, there has been an increasing interest in detecting disease-related rare variants in sequencing studies. Numerous studies have shown that common variants can only explain a small proportion of the phenotypic variance for complex diseases. More and more evidence suggests that some of this missing heritability can be explained by rare variants. Considering the importance of rare variants, researchers have proposed a considerable number of methods for identifying the rare variants associated with complex diseases. Extensive research has been carried out on testing the association between rare variants and dichotomous, continuous or ordinal traits. So far, however, there has been little discussion about the case in which both genotypes and phenotypes are ordinal variables. This paper introduces a method based on the γ-statistic, called OV-RV, for examining disease-related rare variants when both genotypes and phenotypes are ordinal. At present, little is known about the asymptotic distribution of the γ-statistic when conducting association analyses for rare variants. One advantage of OV-RV is that it provides a robust estimation of the distribution of the γ-statistic by employing the permutation approach proposed by Fisher. We also perform extensive simulations to investigate the numerical performance of OV-RV under various model settings. The simulation results reveal that OV-RV is valid and efficient; namely, it controls the type I error approximately at the pre-specified significance level and achieves greater power at the same significance level. We also apply OV-RV for rare variant association studies of diastolic blood pressure.

Indexed as

Computational BiologyComputer SimulationData Interpretation, StatisticalGenetic Predisposition to DiseaseGenetic VariationGenome-Wide Association StudyGenotypeHumansMathematical ComputingModels, GeneticPhenotypeSequence Analysis, DNAcontingency tablesordinal variablesrare variantsγ-statistic

Identifiers

PMID31831092
PMCPMC7044977
OpenAlexW2996194139

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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.