Predicting genetic predisposition in humans: the promise of whole-genome markers
- 3 November 2010
- journal article
- review article
- Published by Springer Science and Business Media LLC in Nature Reviews Genetics
- Vol. 11 (12), 880-886
- https://doi.org/10.1038/nrg2898
Abstract
Prediction of genetic values using whole-genome markers has been successfully applied in commercial breeding. This article outlines the use of this method for predicting health-related outcomes in humans. Although genome-wide association studies have identified markers that are associated with various human traits and diseases, our ability to predict such phenotypes remains limited. A perhaps overlooked explanation lies in the limitations of the genetic models and statistical techniques commonly used in association studies. We propose that alternative approaches, which are largely borrowed from animal breeding, provide potential for advances. We review selected methods and discuss the challenges and opportunities ahead.Keywords
This publication has 52 references indexed in Scilit:
- Common SNPs explain a large proportion of the heritability for human heightNature Genetics, 2010
- Genome-wide Analysis of Genetic Loci Associated With Alzheimer DiseaseJAMA, 2010
- Genes and lifestyle factors in obesity: results from 12 462 subjects from MONICA/KORAInternational Journal of Obesity, 2010
- Genomic selection in plant breeding: from theory to practiceBriefings in Functional Genomics, 2010
- Understanding and using quantitative genetic variationPhilosophical Transactions B, 2010
- The Role of Obesity‐associated Loci Identified in Genome‐wide Association Studies in the Determination of Pediatric BMIObesity, 2009
- Finding the missing heritability of complex diseasesNature, 2009
- A new estimate of family disease history providing improved prediction of disease risksStatistics in Medicine, 2009
- Six new loci associated with body mass index highlight a neuronal influence on body weight regulationNature Genetics, 2008
- Prediction of individual genetic risk to disease from genome-wide association studiesGenome Research, 2007