Methods to infer dense genomic information from sparsely genotyped populations
Methods to infer dense genomic information from sparsely genotyped populations
批准号:
LP100100880
负责人:
Prof Julius van der Werf
金额:
$19.49万
依托单位国家:
澳大利亚
项目类别:
Linkage Projects
财政年份:
2010
资助国家:
澳大利亚
项目状态:
已结题
起止时间:
2010-04-01 至 2013-10-15
中文摘要
基于DNA多态或序列的表型预测在人类医学疾病风险预测和动植物育种遗传值预测等方面有着重要的应用。该项目将提高相关性研究的精确度并降低成本,从而大幅提高此类预测的准确性。这将允许更有效的遗传改良,特别是困难但重要的特征,如抗病能力、减少温室气体排放和产品质量。同样的方法可以推广到改善植物的遗传改良和更好地预测人类疾病风险。
英文摘要
Prediction of phenotype based on DNA polymorphisms or sequence has important applications such as prediction of disease risk in human medicine and prediction of genetic value in plant or animal breeding. This project will enhance precision and lower the cost of association studies leading to substantial increase in accuracy of such predictions. This will allow more effective genetic improvement, particularly of difficult but important traits such as disease resistance, reduced green-house gas emissions and product quality. The same methods can be extended to improve genetic improvement in plants and better prediction of human disease risk.
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