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
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
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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会议论文
Canada Research Chair - Tier 1
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批准号:412102
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项目类别:
-
资助金额:$101.99万
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财政年份:2018
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负责人:Jones Steven
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依托单位:
Modulators of epigenomic processes - a novel approach to cancer therapy
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批准号:323446
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项目类别:Operating Grants
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资助金额:$40.83万
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财政年份:2015
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负责人:Jones Steven
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依托单位:
An Epigenomic Data Coordination Centre for Canada
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批准号:253851
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项目类别:Operating Grants
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资助金额:$80.81万
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财政年份:2011
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负责人:Jones Steven
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依托单位:
CIHR Training Grant in Bioinformatics for Health Research
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批准号:176960
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项目类别:Operating Grants
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资助金额:$142.06万
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财政年份:2008
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负责人:Jones Steven
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依托单位:
海外基金