ArticleBioinformatics (Oxford, England)2017
Conditional asymptotic inference for the kernel association test.
Article in Bioinformatics (Oxford, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00000125 (Ocular Hypertension Treatment Study), which is not on this map. Cited by 2 papers.
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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.
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.
Ocular Hypertension Treatment Study (OHTS)
Who cites it
2 citing papers in PubMed.
- Excalibur: A new ensemble method based on an optimal combination of aggregation tests for rare-variant association testing for sequencing data.PLoS computational biology · 2023Article
- Integration of methylation QTL and enhancer-target gene maps with schizophrenia GWAS summary results identifies novel genes.Bioinformatics (Oxford, England) · 2019Article
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1 author.
Funding
Abstract
motivationThe kernel association test (KAT) is popular in biological studies for its ability to combine weak effects potentially of opposite direction. Its P-value is typically assessed via its (unconditional) asymptotic distribution. However, such an asymptotic distribution is known only for continuous traits and for dichotomous traits. Furthermore, the derived P-values are known to be conservative when sample size is small, especially for the important case of dichotomous traits. One alternative is the permutation test, a widely accepted approximation to the exact finite sample conditional inference. But it is time-consuming to use in practice due to stringent significance criteria commonly seen in these analyses.
resultsBased on a previous theoretical result a conditional asymptotic distribution for the KAT is introduced. This distribution provides an alternative approximation to the exact distribution of the KAT. An explicit expression of this distribution is provided from which P-values can be easily computed. This method applies to any type of traits. The usefulness of this approach is demonstrated via extensive simulation studies using real genotype data and an analysis of genetic data from the Ocular Hypertension Treatment Study. Numerical results showed that the new method can control the type I error rate and is a bit conservative when compared to the permutation method. Nevertheless the proposed method may be used as a fast screening method. A time-consuming permutation procedure may be conducted at locations that show signals of association. AVAILABILITY AND IMPLEMENTATION: An implementation of the proposed method is provided in the R package iGasso. CONTACT: kai-wang@uiowa.edu.
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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.