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

2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Qiuying Sha ◽  
Kui Zhang ◽  
Shuanglin Zhang
2021 ◽  
Author(s):  
Jimmy Mullaert ◽  
Matthieu Bouaziz ◽  
Yoann Seeleuthner ◽  
Benedetta Bigio ◽  
Jean‐Laurent Casanova ◽  
...  

Author(s):  
J. Mullaert ◽  
M. Bouaziz ◽  
Y. Seeleuthner ◽  
B. Bigio ◽  
J-L. Casanova ◽  
...  

AbstractMany methods for rare variant association studies require permutations to assess the significance of tests. Standard permutations assume that all individuals are exchangeable and do not take population stratification (PS), a known confounding factor in genetic studies, into account. We propose a novel strategy, LocPerm, in which individuals are permuted only with their closest ancestry-based neighbors. We performed a simulation study, focusing on small samples, to evaluate and compare LocPerm with standard permutations and classical adjustment on first principal components. Under the null hypothesis, LocPerm was the only method providing an acceptable type I error, regardless of sample size and level of stratification. The power of LocPerm was similar to that of standard permutation in the absence of PS, and remained stable in different PS scenarios. We conclude that LocPerm is a method of choice for taking PS and/or small sample size into account in rare variant association studies.


2016 ◽  
Vol 10 (S7) ◽  
Author(s):  
Huanhuan Zhu ◽  
Zhenchuan Wang ◽  
Xuexia Wang ◽  
Qiuying Sha

2015 ◽  
pp. btv457
Author(s):  
Na Zhu ◽  
Verena Heinrich ◽  
Thorsten Dickhaus ◽  
Jochen Hecht ◽  
Peter N. Robinson ◽  
...  

2019 ◽  
Vol 44 (1) ◽  
pp. 104-116
Author(s):  
Tianzhong Yang ◽  
Junghi Kim ◽  
Chong Wu ◽  
Yiding Ma ◽  
Peng Wei ◽  
...  

2016 ◽  
Vol 24 (9) ◽  
pp. 1344-1351 ◽  
Author(s):  
Jianping Sun ◽  
◽  
Karim Oualkacha ◽  
Vincenzo Forgetta ◽  
Hou-Feng Zheng ◽  
...  

2019 ◽  
Author(s):  
George Kanoungi ◽  
Michael Nothnagel ◽  
Tim Becker ◽  
Dmitriy Drichel

AbstractRegion-based genome-wide scans are usually performed by use of a priori chosen analysis regions. Such an approach will likely miss the region comprising the strongest signal and, thus, may result in increased type II error rates and decreased power. Here, we propose a genomic exhaustive scan approach that analyzes all possible subsequences and does not rely on a prior definition of the analysis regions. As a prime instance, we present a computationally ultra-efficient implementation using the rare-variant collapsing test for phenotypic association, the genomic exhaustive collapsing scan (GECS). Our implementation allows for the identification of regions comprising the strongest signals in large, genome-wide rare-variant association studies while controlling the family-wise error rate via permutation. Application of GECS to two genomic data sets revealed several novel significantly associated regions for age-related macular degeneration and for schizophrenia. Our approach also offers a high potential for genome-wide scans for selection, methylation and other analyses.


Sign in / Sign up

Export Citation Format

Share Document