Literature DB >> 27147090

Association Tests for Rare Variants.

Dan L Nicolae1.   

Abstract

Over the past few years, interest in the identification of rare variants that influence human phenotype has led to the development of many statistical methods for testing for association between sets of rare variants and binary or quantitative traits. Here, I review some of the most important ideas that underlie these methods and the most relevant issues when choosing a method for analysis. In addition to the tests for association, I review crucial issues in performing a rare variant study, from experimental design to interpretation and validation. I also discuss the many challenges of these studies, some of their limitations, and future research directions.

Entities:  

Keywords:  burden test; effect size; exome sequencing; genetic association studies; rare variants; study design; variance components; variant annotation; whole-genome sequencing

Mesh:

Year:  2016        PMID: 27147090     DOI: 10.1146/annurev-genom-083115-022609

Source DB:  PubMed          Journal:  Annu Rev Genomics Hum Genet        ISSN: 1527-8204            Impact factor:   8.929


  14 in total

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Authors:  Zhengdong D Zhang; Sofiya Milman; Jhih-Rong Lin; Shayne Wierbowski; Haiyuan Yu; Nir Barzilai; Vera Gorbunova; Warren C Ladiges; Laura J Niedernhofer; Yousin Suh; Paul D Robbins; Jan Vijg
Journal:  Nat Metab       Date:  2020-07-27

2.  FGWAS: Functional genome wide association analysis.

Authors:  Chao Huang; Paul Thompson; Yalin Wang; Yang Yu; Jingwen Zhang; Dehan Kong; Rivka R Colen; Rebecca C Knickmeyer; Hongtu Zhu
Journal:  Neuroimage       Date:  2017-07-20       Impact factor: 6.556

3.  The contribution of rare genetic variants to the pathogenesis of polycystic ovary syndrome.

Authors:  Matthew Dapas; Andrea Dunaif
Journal:  Curr Opin Endocr Metab Res       Date:  2020-04-03

4.  Integrated rare variant-based risk gene prioritization in disease case-control sequencing studies.

Authors:  Jhih-Rong Lin; Quanwei Zhang; Ying Cai; Bernice E Morrow; Zhengdong D Zhang
Journal:  PLoS Genet       Date:  2017-12-27       Impact factor: 5.917

Review 5.  The impact of rare and low-frequency genetic variants in common disease.

Authors:  Lorenzo Bomba; Klaudia Walter; Nicole Soranzo
Journal:  Genome Biol       Date:  2017-04-27       Impact factor: 13.583

6.  Cis-SNPs Set Testing and PrediXcan Analysis for Gene Expression Data using Linear Mixed Models.

Authors:  Ping Zeng; Ting Wang; Shuiping Huang
Journal:  Sci Rep       Date:  2017-11-10       Impact factor: 4.379

7.  Determining population stratification and subgroup effects in association studies of rare genetic variants for nicotine dependence.

Authors:  Ai-Ru Hsieh; Li-Shiun Chen; Ying-Ju Li; Cathy S J Fann
Journal:  Psychiatr Genet       Date:  2019-08       Impact factor: 2.458

8.  Rare protein-coding variants implicate genes involved in risk of suicide death.

Authors:  Emily DiBlasi; Andrey A Shabalin; Eric T Monson; Brooks R Keeshin; Amanda V Bakian; Anne V Kirby; Elliott Ferris; Danli Chen; Nancy William; Eoin Gaj; Michael Klein; Leslie Jerominski; W Brandon Callor; Erik Christensen; Ken R Smith; Alison Fraser; Zhe Yu; Douglas Gray; Nicola J Camp; Eli A Stahl; Qingqin S Li; Anna R Docherty; Hilary Coon
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2021-05-27       Impact factor: 3.358

9.  A non-threshold region-specific method for detecting rare variants in complex diseases.

Authors:  Ai-Ru Hsieh; Dao-Peng Chen; Amrita Sengupta Chattopadhyay; Ying-Ju Li; Chien-Ching Chang; Cathy S J Fann
Journal:  PLoS One       Date:  2017-11-30       Impact factor: 3.240

10.  IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes.

Authors:  Yukihide Momozawa; Julia Dmitrieva; Emilie Théâtre; Valérie Deffontaine; Souad Rahmouni; Benoît Charloteaux; François Crins; Elisa Docampo; Mahmoud Elansary; Ann-Stephan Gori; Christelle Lecut; Rob Mariman; Myriam Mni; Cécile Oury; Ilya Altukhov; Dmitry Alexeev; Yuri Aulchenko; Leila Amininejad; Gerd Bouma; Frank Hoentjen; Mark Löwenberg; Bas Oldenburg; Marieke J Pierik; Andrea E Vander Meulen-de Jong; C Janneke van der Woude; Marijn C Visschedijk; Mark Lathrop; Jean-Pierre Hugot; Rinse K Weersma; Martine De Vos; Denis Franchimont; Severine Vermeire; Michiaki Kubo; Edouard Louis; Michel Georges
Journal:  Nat Commun       Date:  2018-06-21       Impact factor: 14.919

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