## Abstract Nextβgeneration sequencing technology allows investigation of both common and rare variants in humans. Exomes are sequenced on the population level or in families to further study the genetics of human diseases. Genetic Analysis Workshop 17 (GAW17) provided exomic data from the 1000 Gen
Statistical analysis of rare sequence variants: an overview of collapsing methods
β Scribed by Carmen Dering; Claudia Hemmelmann; Elizabeth Pugh; Andreas Ziegler
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 99 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0741-0395
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β¦ Synopsis
Abstract
With the advent of novel sequencing technologies, interest in the identification of rare variants that influence common traits has increased rapidly. Standard statistical methods, such as the CochraneβArmitage trend test or logistic regression, fail in this setting for the analysis of unrelated subjects because of the rareness of the variants. Recently, various alternative approaches have been proposed that circumvent the rareness problem by collapsing rare variants in a defined genetic region or sets of regions. We provide an overview of these collapsing methods for association analysis and discuss the use of permutation approaches for significance testing of the dataβadaptive methods. Genet. Epidemiol. 35:S12βS17, 2011. Β© 2011 Wiley Periodicals, Inc.
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