Association Analysis and Meta-Analysis of Multi-allelic Variants for Large Scale Sequence Data
Xiaowei ZhaniD, Sai CheniD, Yu JiangiD, Mengzhen LiuiD, William G. IaconoiD, John K. HewittiD, John E. HokansoniD, Kenneth S. KrauteriD, Markku LaaksoiD, Kevin W. Li, Sharon Marie LutziD, Matthew McGue, Anita PanditiD, Gregory J. M. ZajaciD, Michael BoehnkeiD, Gonçalo R. AbecasisiD, Bibo JiangiD, Scott I. VriezeiD, Dajiang J. LiuiD
Abstract
MotivationThere is great interest to understand the impact of rare variants in human diseases using large sequence datasets. In deep sequences datasets of >10,000 samples, [~]10% of the variant sites are observed to be multi-allelic. Many of the multi-allelic variants have been shown to be functional and disease relevant. Proper analysis of multi-allelic variants is critical to the success of a sequencing study, but existing methods do not properly handle multi-allelic variants and can produce highly misleading association results.\n\nResultsWe propose novel methods to encode multi-allelic sites, conduct single variant and gene-level association analyses, and perform meta-analysis for multi-allelic variants. We evaluated these methods through extensive simulations and the study of a large meta-analysis of [~]18,000 samples on the cigarettes-per-day phenotype. We showed that our joint modeling approach provided an unbiased estimate of genetic effects, greatly improved the power of single variant association tests, and enhanced gene-level tests over existing approaches.\n\nAvailabilitySoftware packages implementing these methods are available at (https://github.com/zhanxw/rvtests http://genome.sph.umich.edu/wiki/RareMETAL).\n\nContactxiaowei.zhan@utsouthwestem.edu; dajiang.liu@psu.edu
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 2
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Inferring Disease Risk Genes from Sequencing Data in Multiplex Pedigrees Through Sharing of Rare Variants
Alexandre Bureau, Ferdouse Begum, … Ingo Ruczinski·Genetic EpidemiologyPeer-reviewed·Sep 24, 2018
- Testing an Optimally Weighted Combination of Common and/or Rare Variants with Multiple Traits
Zhenchuan Wang, Qiuying Sha, … Shuanglin Zhang·PLoS ONEPeer-reviewed·Jul 26, 2018
- Meta-MultiSKAT: Multiple phenotype meta-analysis for region-based association test
Diptavo Dutta, Sarah A. Gagliano Taliun, … Seunggeun Lee·Genetic EpidemiologyPeer-reviewed·Aug 21, 2019
- Multi-SKAT: General framework to test multiple phenotype associations of rare variants
Diptavo Dutta, Laura Scott, … Seunggeun Lee·bioRxiv·Jul 30, 2018
- Computationally efficient meta-analysis of gene-based tests using summary statistics in large-scale genetic studies
Tyler Joseph, Joelle S. Mbatchou, … Jonathan Marchini·Nature GeneticsPeer-reviewed·Nov 12, 2025
- Bayesian mixture model for clustering rare-variant effects in human genetic studies
Guhan Ram Venkataraman, Yosuke Tanigawa, … Manuel A. Rivas·bioRxiv·Aug 3, 2021