Uncovering complex genetic mechanisms of disease

揭示疾病的复杂遗传机制

• 批准号: 472590
• 负责人: Tarailo-Graovac Maja
• 金额: $ 7.29万
• 依托单位: University of Calgary
• 依托单位国家: 加拿大
• 项目类别: Operating Grants
• 财政年份: 2022
• 资助国家: 加拿大
• 起止时间: 2022-09-01 至 2023-09-01
• 项目状态: 已结题
• 来源: https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=472590&lang=en
• 关键词: Bioinformatics; Complex Variants; Genome Sequencing; Genomics; Mechanism Of A Disease; Model Organism; Non-Coding Variants; Rare Disease; Structural Variants; Transcriptomics

Genetic diseases result from alterations of genetic material that lead to functional impact on genes. Despite the recent advancements in genomics that have facilitated sequencing of individual human genomes, the genetic cause is difficult to identify in t

遗传疾病是由于遗传物质的改变导致基因功能的影响。尽管最近基因组学的进步促进了个体人类基因组的测序，但很难确定其遗传原因