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Evaluating the utility of long-read genome sequencing for uncovering causal genetic variation and epigenetic signatures of rare disease

Evaluating the utility of long-read genome sequencing for uncovering causal genetic variation and epigenetic signatures of rare disease
评估长读长基因组测序在揭示罕见疾病的因果遗传变异和表观遗传特征方面的效用
批准号:
470437
负责人:
Jones Steven
金额:
$59.63万
依托单位:
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
项目状态:
未结题
起止时间:
2022-09-01 至 2026-09-01

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中文摘要
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英文摘要
Rare diseases collectively affect millions of people worldwide. The majority of rare diseases are caused by harmful genetic changes that are inherited from a parent or arise during development by chance. Unfortunately, the cause of disease in many individ
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Canada Research Chair - Tier 1
  • 批准号:
    412102
  • 项目类别:
  • 资助金额:
    $101.99万
  • 财政年份:
    2018
  • 负责人:
    Jones Steven
  • 依托单位:
Modulators of epigenomic processes - a novel approach to cancer therapy
  • 批准号:
    323446
  • 项目类别:
    Operating Grants
  • 资助金额:
    $40.83万
  • 财政年份:
    2015
  • 负责人:
    Jones Steven
  • 依托单位:
An Epigenomic Data Coordination Centre for Canada
  • 批准号:
    253851
  • 项目类别:
    Operating Grants
  • 资助金额:
    $80.81万
  • 财政年份:
    2011
  • 负责人:
    Jones Steven
  • 依托单位:
CIHR Training Grant in Bioinformatics for Health Research
  • 批准号:
    176960
  • 项目类别:
    Operating Grants
  • 资助金额:
    $142.06万
  • 财政年份:
    2008
  • 负责人:
    Jones Steven
  • 依托单位:
海外基金