Literature DB >> 15583426

A note on inference of trait associations with SNP haplotypes and other attributes in generalized linear models.

Kelly Burkett1, Brad McNeney, Jinko Graham.   

Abstract

Recently, Lake et al. [Human Heredity 2003;55:56-65] have proposed an approach based on the EM algorithm for maximum-likelihood inference of trait associations with haplotypes and environmental cofactors in generalized linear models. In this short report, we describe an extension to accommodate missing SNP genotype information. We also discuss differences in the calculation of standard errors between their implementation and our own. Finally, we present results indicating that inference is robust to low levels of dependence between haplotypes and nongenetic factors, but that biased inference can result when there is moderate to strong dependence. Overall, the method is found to perform well in the models we considered. Copyright (c) 2004 S. Karger AG, Basel.

Entities:  

Mesh:

Year:  2004        PMID: 15583426     DOI: 10.1159/000081447

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  14 in total

1.  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

2.  Association of Hck genetic polymorphisms with gene expression and COPD.

Authors:  Xiaozhu Zhang; Salahaddin Mahmudi-Azer; John E Connett; Nicholas R Anthonisen; Jian-Qing He; Peter D Paré; Andrew J Sandford
Journal:  Hum Genet       Date:  2006-09-26       Impact factor: 4.132

3.  Generalized linear modeling with regularization for detecting common disease rare haplotype association.

Authors:  Wei Guo; Shili Lin
Journal:  Genet Epidemiol       Date:  2009-05       Impact factor: 2.135

4.  Comparison of haplotype-based tests for detecting gene-environment interactions with rare variants.

Authors:  Charalampos Papachristou; Swati Biswas
Journal:  Brief Bioinform       Date:  2020-05-21       Impact factor: 11.622

5.  Association between polymorphisms of complement pathway genes and age-related macular degeneration in a Chinese population.

Authors:  Lin Wu; Qiushan Tao; Wen Chen; Zhi Wang; Yanping Song; Shuangyan Sheng; Pengcheng Li; Jingjing Zhou
Journal:  Invest Ophthalmol Vis Sci       Date:  2013-01-07       Impact factor: 4.799

6.  Multivariate meta-analysis of the association of G-protein beta 3 gene (GNB3) haplotypes with cardiovascular phenotypes.

Authors:  Tiago V Pereira; Lilian Kimura; Yasushi Suwazono; Hideaki Nakagawa; Makoto Daimon; Toshihide Oizumi; Takamasa Kayama; Takeo Kato; Liao Li; Shufeng Chen; Dongfeng Gu; Wilfried Renner; Winfried März; Yoshiji Yamada; Pantelis G Bagos; Regina C Mingroni-Netto
Journal:  Mol Biol Rep       Date:  2014-01-30       Impact factor: 2.316

7.  Interferon gamma polymorphisms and their interaction with smoking are associated with lung function.

Authors:  Jian-Qing He; Kelly Burkett; John E Connett; Nicholas R Anthonisen; Peter D Paré; Andrew J Sandford
Journal:  Hum Genet       Date:  2006-02-11       Impact factor: 4.132

8.  Haplotype association analysis of North American Rheumatoid Arthritis Consortium data using a generalized linear model with regularization.

Authors:  Wei Guo; Chin-Yuan Liang; Shili Lin
Journal:  BMC Proc       Date:  2009-12-15

9.  Genetic variants of GCH1 associate with chronic and acute crisis pain in African Americans with sickle cell disease.

Authors:  Nilanjana Sadhu; Ellie H Jhun; Yingwei Yao; Ying He; Robert E Molokie; Diana J Wilkie; Zaijie Jim Wang
Journal:  Exp Hematol       Date:  2018-07-19       Impact factor: 3.084

Review 10.  Integrated analysis of genetic data with R.

Authors:  Jing Hua Zhao; Qihua Tan
Journal:  Hum Genomics       Date:  2006-01       Impact factor: 4.639

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.