Structural variation in medical genomics

医学基因组学的结构变异

• 批准号: 190000
• 负责人: Scherer Stephen W
• 金额: $ 76.53万
• 依托单位: Hospital for Sick Children (Toronto)
• 依托单位国家: 加拿大
• 项目类别: Operating Grants
• 财政年份: 2009
• 资助国家: 加拿大
• 起止时间: 2009-09-01 至 2014-09-01
• 项目状态: 已结题
• 来源: https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=190000&lang=en
• 关键词: Cytogenomics; Disease Predisposition; Dna And Chromosome Variation; Genomic Microarrary; Quantitative And Copy Number Analysis

Genetic variation forms the basis of evolution and human diversity. In some instances deleterious changes in DNA can occur resulting in disease. The Human Genome Project told us we were 99.9% DNA identical with the majority of changes in our genomes being

遗传变异是进化和人类多样性的基础。在某些情况下，DNA的有害变化可能导致疾病。人类基因组计划告诉我们，我们的DNA有99.9%是相同的，我们基因组的大部分变化都是相同的