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Genome-wide discovery of the causative mutations in hereditary cancers using next-generation RNA and exomic sequencing of human tumour samples.

Genome-wide discovery of the causative mutations in hereditary cancers using next-generation RNA and exomic sequencing of human tumour samples.
使用新一代 RNA 和人类肿瘤样本的外显子组测序，在全基因组范围内发现遗传性癌症的致病突变。
批准号：
229572
负责人：
Lalonde Emilie R
金额：
$7.65万
依托单位：
McGill University
依托单位国家：
加拿大
项目类别：
Studentship Programs
财政年份：
2010
资助国家：
加拿大
项目状态：
已结题
起止时间：
2010-10-01 至 2013-10-01
来源：
https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=229572&lang=en
关键词：
Bioinformatics Genetics Of Cancer Genome Alterations Genomics/Transcriptomics Hereditary Cancers Next-Generation Sequencing Transcript Alteration

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中文摘要
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英文摘要
The completion of the Human Genome Project was hailed as a major milestone in science. This 13-year project required hundreds of scientists and billions of dollars. Now, with the advent of next-generation sequencing (NGS), we can achieve the same result i
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A radiomics investigation into the heterogeneity of head and neck cancers
Detecting novel splice variants contributing to breast cancer using next-generation mRNA sequencing.
  • 批准号：
    200314
  • 项目类别：
    Studentship Programs
  • 资助金额：
    $1.27万
  • 财政年份：
    2010
  • 负责人：
    Lalonde Emilie R
  • 依托单位：
    McGill University
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