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The application of next-generation sequencing technology in identifying the genetic origins of unclassified familial disorders.

The application of next-generation sequencing technology in identifying the genetic origins of unclassified familial disorders.
下一代测序技术在鉴定未分类家族性疾病的遗传起源中的应用。
批准号：
327808
负责人：
Farhan Sali M
金额：
$7.65万
依托单位：
University of Western Ontario
依托单位国家：
加拿大
项目类别：
Studentship Programs
财政年份：
2014
资助国家：
加拿大
项目状态：
已结题
起止时间：
2014-10-01 至 2017-10-01
来源：
https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=327808&lang=en
关键词：
Amyotrophic Lateral Sclerosis Clinical Diagnoses Gene Panels Late-Onset Neurodegenerative Disorders Neurology Next-Generation Sequencing Population Health Rare Genetic Disorders Whole-Exome Sequencing

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中文摘要
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英文摘要
The decreasing cost of decoding the hereditary information contained in our cells has made genetic sequencing a central component in medicine. With the help of next-generation sequencing (NGS) technology, a new genetic tool, we can now identify a wide ran
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Applying genome sequence analysis tools in human diseases.
Next-generation sequencing elucidates the genetic aetiology of novel and rare paediatric disorders in founder populations.
  • 批准号：
    294385
  • 项目类别：
  • 资助金额：
    $0.07万
  • 财政年份：
    2013
  • 负责人：
    Farhan Sali M
  • 依托单位：
    University of Western Ontario
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