Literature DB >> 28980243

Testing Departure from Hardy-Weinberg Proportions.

Jian Wang1, Sanjay Shete2,3.   

Abstract

The Hardy-Weinberg principle, one of the most important principles in population genetics, was originally developed for the study of allele frequency changes in a population over generations. It is now, however, widely used in studies of human diseases to detect inbreeding, population stratification, and genotyping errors. For assessment of deviation from Hardy-Weinberg proportions in data, the most popular approaches include the asymptotic Pearson's chi-squared goodness-of-fit test and the exact test. Pearson's chi-squared goodness-of-fit test is simple and straightforward, but is very sensitive to a small sample size or rare allele frequency. The exact test of Hardy-Weinberg proportions is preferable in these situations. The exact test can be performed through complete enumeration of heterozygote genotypes or on the basis of the Markov chain Monte Carlo procedure. In this chapter, we describe the Hardy-Weinberg principle and the commonly used Hardy-Weinberg proportion tests and their applications, and we demonstrate how the chi-squared test and exact test of Hardy-Weinberg proportions can be performed step-by-step using the popular software programs SAS, R, and PLINK, which have been widely used in genetic association studies, along with numerical examples. We also discuss approaches for testing Hardy-Weinberg proportions in case-control study designs that are better than traditional approaches for testing Hardy-Weinberg proportions in controls only. Finally, we note that deviation from the Hardy-Weinberg proportions in affected individuals can provide evidence for an association between genetic variants and diseases.

Entities:  

Keywords:  Case–control genetic association study; Exact test; Genetic association study; Genotyping error; Hardy-Weinberg proportions; PLINK; Pearson’s chi-squared goodness-of-fit test; Population stratification; Quality control; R; SAS/genetics

Mesh:

Year:  2017        PMID: 28980243     DOI: 10.1007/978-1-4939-7274-6_6

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  7 in total

1.  The molecular genetic background leading to the formation of the human erythroid-specific Xga/CD99 blood groups.

Authors:  Chih-Chun Yeh; Ching-Jin Chang; Yuh-Ching Twu; Chen-Chung Chu; Bi-Shan Liu; Ji-Ting Huang; Shu-Ting Hung; Yung-Syu Chan; Yi-Jui Tsai; Sheng-Wei Lin; Marie Lin; Lung-Chih Yu
Journal:  Blood Adv       Date:  2018-08-14

2.  Establishing analytical validity of BeadChip array genotype data by comparison to whole-genome sequence and standard benchmark datasets.

Authors:  Praveen F Cherukuri; Melissa M Soe; David E Condon; Shubhi Bartaria; Kaitlynn Meis; Shaopeng Gu; Frederick G Frost; Lindsay M Fricke; Krzysztof P Lubieniecki; Joanna M Lubieniecka; Robert E Pyatt; Catherine Hajek; Cornelius F Boerkoel; Lynn Carmichael
Journal:  BMC Med Genomics       Date:  2022-03-14       Impact factor: 3.063

3.  Genome-wide association study identifies genes associated with neuropathy in patients with head and neck cancer.

Authors:  Cielito C Reyes-Gibby; Jian Wang; Sai-Ching J Yeung; Patrick Chaftari; Robert K Yu; Ehab Y Hanna; Sanjay Shete
Journal:  Sci Rep       Date:  2018-06-08       Impact factor: 4.379

4.  The minor T allele of the MUC5B promoter rs35705950 associated with susceptibility to idiopathic pulmonary fibrosis: a meta-analysis.

Authors:  Xiaozheng Wu; Wen Li; Zhenliang Luo; Yunzhi Chen
Journal:  Sci Rep       Date:  2021-12-14       Impact factor: 4.379

5.  A systematic review and meta-analysis expounding the relationship between methylene tetrahydrofolate reductase gene polymorphism and the risk of intracerebral hemorrhage among populations.

Authors:  Xue-Lun Zou; Tian-Xing Yao; Lu Deng; Lei Chen; Ye Li; Le Zhang
Journal:  Front Genet       Date:  2022-08-03       Impact factor: 4.772

6.  Increased frequency of angiotensin converting enzyme D allele in Chinese Han patients with idiopathic pulmonary fibrosis: A systematic review and meta-analysis.

Authors:  Xiaozheng Wu; Wen Li; Gao Huang; Zhenliang Luo; Yunzhi Chen
Journal:  Medicine (Baltimore)       Date:  2022-10-07       Impact factor: 1.817

7.  Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases.

Authors:  Atsushi Kondo; China Nagano; Shinya Ishiko; Takashi Omori; Yuya Aoto; Rini Rossanti; Nana Sakakibara; Tomoko Horinouchi; Tomohiko Yamamura; Sadayuki Nagai; Eri Okada; Yuko Shima; Koichi Nakanishi; Takeshi Ninchoji; Hiroshi Kaito; Hiroki Takeda; Hiroaki Nagase; Naoya Morisada; Kazumoto Iijima; Kandai Nozu
Journal:  Sci Rep       Date:  2021-08-09       Impact factor: 4.379

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.