Literature DB >> 22128052

Statistical analysis of rare sequence variants: an overview of collapsing methods.

Carmen Dering1, Claudia Hemmelmann, Elizabeth Pugh, Andreas Ziegler.   

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 Cochrane-Armitage 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 data-adaptive methods.
© 2011 Wiley Periodicals, Inc.

Entities:  

Mesh:

Year:  2011        PMID: 22128052      PMCID: PMC3277891          DOI: 10.1002/gepi.20643

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  29 in total

1.  SIFT: Predicting amino acid changes that affect protein function.

Authors:  Pauline C Ng; Steven Henikoff
Journal:  Nucleic Acids Res       Date:  2003-07-01       Impact factor: 16.971

2.  Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data.

Authors:  Bingshan Li; Suzanne M Leal
Journal:  Am J Hum Genet       Date:  2008-08-07       Impact factor: 11.025

3.  Personal genomes: The case of the missing heritability.

Authors:  Brendan Maher
Journal:  Nature       Date:  2008-11-06       Impact factor: 49.962

4.  A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST).

Authors:  Stephan Morgenthaler; William G Thilly
Journal:  Mutat Res       Date:  2006-11-13       Impact factor: 2.433

5.  Human non-synonymous SNPs: server and survey.

Authors:  Vasily Ramensky; Peer Bork; Shamil Sunyaev
Journal:  Nucleic Acids Res       Date:  2002-09-01       Impact factor: 16.971

6.  A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes.

Authors:  Douglas F Easton; Amie M Deffenbaugh; Dmitry Pruss; Cynthia Frye; Richard J Wenstrup; Kristina Allen-Brady; Sean V Tavtigian; Alvaro N A Monteiro; Edwin S Iversen; Fergus J Couch; David E Goldgar
Journal:  Am J Hum Genet       Date:  2007-09-06       Impact factor: 11.025

7.  A groupwise association test for rare mutations using a weighted sum statistic.

Authors:  Bo Eskerod Madsen; Sharon R Browning
Journal:  PLoS Genet       Date:  2009-02-13       Impact factor: 5.917

8.  SNAP predicts effect of mutations on protein function.

Authors:  Yana Bromberg; Guy Yachdav; Burkhard Rost
Journal:  Bioinformatics       Date:  2008-08-30       Impact factor: 6.937

9.  Fewer permutations, more accurate P-values.

Authors:  Theo A Knijnenburg; Lodewyk F A Wessels; Marcel J T Reinders; Ilya Shmulevich
Journal:  Bioinformatics       Date:  2009-06-15       Impact factor: 6.937

10.  SNPs3D: candidate gene and SNP selection for association studies.

Authors:  Peng Yue; Eugene Melamud; John Moult
Journal:  BMC Bioinformatics       Date:  2006-03-22       Impact factor: 3.169

View more
  110 in total

1.  Multiple testing in high-throughput sequence data: experiences from Group 8 of Genetic Analysis Workshop 17.

Authors:  Inke R König; Jeremie Nsengimana; Charalampos Papachristou; Matthew A Simonson; Kai Wang; Jason A Weisburd
Journal:  Genet Epidemiol       Date:  2011       Impact factor: 2.135

2.  Statistical tests for detecting rare variants using variance-stabilising transformations.

Authors:  Kai Wang; John H Fingert
Journal:  Ann Hum Genet       Date:  2012-06-25       Impact factor: 1.670

Review 3.  Integration of biological networks and pathways with genetic association studies.

Authors:  Yan V Sun
Journal:  Hum Genet       Date:  2012-07-10       Impact factor: 4.132

4.  Comparison of haplotype-based statistical tests for disease association with rare and common variants.

Authors:  Ananda S Datta; Swati Biswas
Journal:  Brief Bioinform       Date:  2015-09-02       Impact factor: 11.622

5.  PI3K/Akt/mTOR Signaling and Plasma Membrane Proteins Are Implicated in Responsiveness to Adjuvant Dendritic Cell Vaccination for Metastatic Colorectal Cancer.

Authors:  David C Qian; Xiangjun Xiao; Jinyoung Byun; Arief A Suriawinata; Stephanie C Her; Christopher I Amos; Richard J Barth
Journal:  Clin Cancer Res       Date:  2016-07-19       Impact factor: 12.531

Review 6.  Network.assisted analysis to prioritize GWAS results: principles, methods and perspectives.

Authors:  Peilin Jia; Zhongming Zhao
Journal:  Hum Genet       Date:  2014-02       Impact factor: 4.132

7.  A large-scale screen for coding variants predisposing to psoriasis.

Authors:  Huayang Tang; Xin Jin; Yang Li; Hui Jiang; Xianfa Tang; Xu Yang; Hui Cheng; Ying Qiu; Gang Chen; Junpu Mei; Fusheng Zhou; Renhua Wu; Xianbo Zuo; Yong Zhang; Xiaodong Zheng; Qi Cai; Xianyong Yin; Cheng Quan; Haojing Shao; Yong Cui; Fangzhen Tian; Xia Zhao; Hong Liu; Fengli Xiao; Fengping Xu; Jianwen Han; Dongmei Shi; Anping Zhang; Cheng Zhou; Qibin Li; Xing Fan; Liya Lin; Hongqing Tian; Zaixing Wang; Huiling Fu; Fang Wang; Baoqi Yang; Shaowei Huang; Bo Liang; Xuefeng Xie; Yunqing Ren; Qingquan Gu; Guangdong Wen; Yulin Sun; Xueli Wu; Lin Dang; Min Xia; Junjun Shan; Tianhang Li; Lin Yang; Xiuyun Zhang; Yuzhen Li; Chundi He; Aie Xu; Liping Wei; Xiaohang Zhao; Xinghua Gao; Jinhua Xu; Furen Zhang; Jianzhong Zhang; Yingrui Li; Liangdan Sun; Jianjun Liu; Runsheng Chen; Sen Yang; Jun Wang; Xuejun Zhang
Journal:  Nat Genet       Date:  2013-11-10       Impact factor: 38.330

8.  Rare Variants of the Serotonin Transporter Are Associated With Psychiatric Comorbidity in Irritable Bowel Syndrome.

Authors:  Ruth Kohen; Julia H Tracy; Eric Haugen; Kevin C Cain; Monica E Jarrett; Margaret M Heitkemper
Journal:  Biol Res Nurs       Date:  2016-02-24       Impact factor: 2.522

9.  Adjustment for population stratification via principal components in association analysis of rare variants.

Authors:  Yiwei Zhang; Weihua Guan; Wei Pan
Journal:  Genet Epidemiol       Date:  2012-10-12       Impact factor: 2.135

10.  A geometric framework for evaluating rare variant tests of association.

Authors:  Keli Liu; Shannon Fast; Matthew Zawistowski; Nathan L Tintle
Journal:  Genet Epidemiol       Date:  2013-03-21       Impact factor: 2.135

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.