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A Platform for Large-Scale Genomic Discovery

A Platform for Large-Scale Genomic Discovery
大规模基因组发现平台
批准号:
8583329
负责人:
RICHARD K. WILSON
金额:
$2558.94万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-11-10 至 2015-10-31

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中文摘要
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英文摘要
Over the past four years, a remarkable sequencing technology explosion has occurred, opening many new avenues of biological experimentation and discovery. We describe a platform for large- scale sequencing and analysis that extends the incredible potential of next-generation sequencing to transform biomedical research and significantly impact medical practice. Our eight specific aims are intertwined across six major research areas that overall address the NHGRI mission and provide an interdisciplinary approach that is already producing medically relevant results in the areas of cancer genomics, heritable disease, and microbial/metagenomics. Our platform offers a consistently cost-effective approach to sequencing-related research projects and we have established a scalable incoming sample pipeline that can intake and track >40,000 samples per year into a flexible and innovative sequencing pipeline. Equally scalable are our LIMS and analysis pipeline capabilities, having established systems that processed several hundred cancer cases through whole genome sequencing and analysis in the last year alone, along with multiple other project types. We describe a research plan that will further our explorations of human health and disease, in a more comprehensive manner than ever before, and will investigate third-generation sequencing technologies, incorporating their unique attributes and integrating them to our production repertoire. One important aspect of our proposed work includes efforts to begin translating our discoveries and procedures into the clinical setting, effectively setting the stage for genomic diagnosis and personalized medicine. This important transition will be required to bring DNA sequencing to clinical medicine, and our innovative combination of sequencing technology, data analysis, and outstanding clinical collaborators increase the potential for success. Overall, we are enthusiastic about the future of genome sequencing at high scale, and we combine years of success in DNA sequencing and analysis with the necessary collaboration expertise, infrastructure support, and shared vision with NHGRI to make significant progress on these aims in the next four years.
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Supplement Proposal: Accelerated Genome Aggregation and Joint Variant Calling Effort
  • 批准号:
    9318798
  • 项目类别:
  • 资助金额:
    $22.45万
  • 财政年份:
    2016
  • 负责人:
    RICHARD K. WILSON
  • 依托单位:
Improving the Human Reference Genome Resource
Improving the Human Reference Genome Resource
  • 批准号:
    8667135
  • 项目类别:
  • 资助金额:
    $289.24万
  • 财政年份:
    2014
  • 负责人:
    RICHARD K. WILSON
  • 依托单位:
Improving the Human Reference Genome Resource
  • 批准号:
    8927670
  • 项目类别:
  • 资助金额:
    $277.97万
  • 财政年份:
    2014
  • 负责人:
    RICHARD K. WILSON
  • 依托单位:
海外基金