Literature DB >> 18388693

Common statistical issues in genome-wide association studies: a review on power, data quality control, genotype calling and population structure.

Yik Y Teo1.   

Abstract

PURPOSE OF REVIEW: Genetic association studies which survey the entire genome have become a common design for uncovering the genetic basis of common diseases, including lipid-related traits. Such studies have identified several novel loci which influence blood lipids. The present review highlights the statistical challenges associated with such large-scale genetic studies and discusses the available methodological strategies for handling these issues. RECENT
FINDINGS: The successful analysis of genome-wide data assayed on commercial genotyping arrays depends on careful exploration of the data. Unaccounted sample failures, genotyping errors and population structure can introduce misleading signals that mimic genuine association. Careful interpretation of useful summary statistics and graphical data displays can minimize the extent of false associations that need to be followed up in replication or fine-mapping experiments.
SUMMARY: Recently published genome-wide studies are beginning to yield valuable insights into the importance of well designed methodological and statistical techniques for sensible interpretation of the plethora of genetic data generated.

Entities:  

Mesh:

Year:  2008        PMID: 18388693     DOI: 10.1097/MOL.0b013e3282f5dd77

Source DB:  PubMed          Journal:  Curr Opin Lipidol        ISSN: 0957-9672            Impact factor:   4.776


  38 in total

1.  A quality control algorithm for filtering SNPs in genome-wide association studies.

Authors:  Monnat Pongpanich; Patrick F Sullivan; Jung-Ying Tzeng
Journal:  Bioinformatics       Date:  2010-05-25       Impact factor: 6.937

Review 2.  Pharmacogenetics of antidepressant response.

Authors:  Stefano Porcelli; Antonio Drago; Chiara Fabbri; Sara Gibiino; Raffaella Calati; Alessandro Serretti
Journal:  J Psychiatry Neurosci       Date:  2011-03       Impact factor: 6.186

3.  Evaluating variations of genotype calling: a potential source of spurious associations in genome-wide association studies.

Authors:  Huixiao Hong; Zhenqiang Su; Weigong Ge; Leming Shi; Roger Perkins; Hong Fang; Donna Mendrick; Weida Tong
Journal:  J Genet       Date:  2010-04       Impact factor: 1.166

4.  Defining a comprehensive verotype using electronic health records for personalized medicine.

Authors:  Mary Regina Boland; George Hripcsak; Yufeng Shen; Wendy K Chung; Chunhua Weng
Journal:  J Am Med Inform Assoc       Date:  2013-09-03       Impact factor: 4.497

5.  Genome-wide strategies for discovering genetic influences on cognition and cognitive disorders: methodological considerations.

Authors:  Steven G Potkin; Jessica A Turner; Guia Guffanti; Anita Lakatos; Federica Torri; David B Keator; Fabio Macciardi
Journal:  Cogn Neuropsychiatry       Date:  2009       Impact factor: 1.871

6.  Genetics and brain morphology.

Authors:  Lachlan T Strike; Baptiste Couvy-Duchesne; Narelle K Hansell; Gabriel Cuellar-Partida; Sarah E Medland; Margaret J Wright
Journal:  Neuropsychol Rev       Date:  2015-03-14       Impact factor: 7.444

7.  Testing gene-gene interactions in genome wide association studies.

Authors:  Jie Kate Hu; Xianlong Wang; Pei Wang
Journal:  Genet Epidemiol       Date:  2014-01-15       Impact factor: 2.135

8.  Look who is calling: a comparison of genotype calling algorithms.

Authors:  Maren Vens; Arne Schillert; Inke R König; Andreas Ziegler
Journal:  BMC Proc       Date:  2009-12-15

9.  On quality control measures in genome-wide association studies: a test to assess the genotyping quality of individual probands in family-based association studies and an application to the HapMap data.

Authors:  David W Fardo; Iuliana Ionita-Laza; Christoph Lange
Journal:  PLoS Genet       Date:  2009-07-24       Impact factor: 6.020

10.  ACPA: automated cluster plot analysis of genotype data.

Authors:  Arne Schillert; Daniel F Schwarz; Maren Vens; Silke Szymczak; Inke R König; Andreas Ziegler
Journal:  BMC Proc       Date:  2009-12-15
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