scholarly journals Power Analysis for Genetic Association Test (PAGEANT) provides insights to challenges for rare variant association studies

2017 ◽  
Vol 34 (9) ◽  
pp. 1506-1513 ◽  
Author(s):  
Andriy Derkach ◽  
Haoyu Zhang ◽  
Nilanjan Chatterjee
2016 ◽  
Vol 10 (S7) ◽  
Author(s):  
Huanhuan Zhu ◽  
Zhenchuan Wang ◽  
Xuexia Wang ◽  
Qiuying Sha

2020 ◽  
Vol 10 ◽  
Author(s):  
Anthony Piot ◽  
Julien Prunier ◽  
Nathalie Isabel ◽  
Jaroslav Klápště ◽  
Yousry A. El-Kassaby ◽  
...  

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

2016 ◽  
Vol 41 (3) ◽  
pp. 198-209 ◽  
Author(s):  
Selyeong Lee ◽  
Sungho Won ◽  
Young Jin Kim ◽  
Yongkang Kim ◽  
Bong-Jo Kim ◽  
...  

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.


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