I-Corps: A cloud-based searchable catalog to link geographically and population diverse patient genomic, phenotypic and clinical data

I-Corps:基于云的可搜索目录,用于链接地理和人群不同的患者基因组、表型和临床数据

基本信息

  • 批准号:
    2029812
  • 负责人:
  • 金额:
    $ 5万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
    Standard Grant
  • 财政年份:
    2020
  • 资助国家:
    美国
  • 起止时间:
    2020-06-01 至 2021-11-30
  • 项目状态:
    已结题

项目摘要

The broader impact/commercial potential of this I-Corps project is to develop a cloud-based, searchable catalog to provide access to global patient data that can be used to provide improved treatments for patients. Currently, there are many questions that require the ability to link and analyze patient data. The problem is that the majority of patient data currently used comes from the same few institutions in Northern Europe that lack geographic or population diversity. The result is that the patient data has limited use for questions related to populations that do not derive from Northern Europe. The patient dataset under development will allow academic and commercial institutions to ask questions that link patient data from around the world to get answers that are applicable to all patient populations. The data will be available to physicians treating patients to ensure more precise treatments and prescription of drugs. The data also will allow research institutions and commercial enterprises to develop drugs and speed their delivery to market by shortening clinical trials. This I-Corps project is based on the development of a single cloud-based, searchable data catalog containing patient genomic, phenotypic and clinical data from geographically diverse populations and a research environment within which the data can be analyzed. The ability to use patient data from geographically diverse patient populations will allow for the ability to determine patient-specific treatments with a high degree of precision, not just for those with a Northern European background, but patients everywhere. Academic and commercial institutions will be able to improve their research and expedite results by analyzing patients' data from geographically diverse regions to answer questions in a few hours or days that currently takes years. It will allow commercial institutions to expedite therapeutic research and streamline clinical trials. The result will be more drugs making it through clinical trials for more diseases in a shorter time for less money. The patient data set also will allow commercial institutions to find patients with rare diseases using genetic analysis from different geographies, instead of the current practice of extrapolating based on a doctor-determined prognosis. The goal is to improve medical research and patient treatment where patient data is used.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
这个I-Corps项目更广泛的影响/商业潜力是开发一个基于云的可搜索目录,以提供对全球患者数据的访问,这些数据可用于为患者提供更好的治疗。 目前,有许多问题需要链接和分析患者数据的能力。问题是,目前使用的大部分患者数据来自北方少数几个缺乏地理或人口多样性的机构。结果是,患者数据对于与非来自北方欧洲的人群相关的问题的使用有限。正在开发的患者数据集将允许学术和商业机构提出问题,将来自世界各地的患者数据联系起来,以获得适用于所有患者人群的答案。这些数据将提供给治疗患者的医生,以确保更精确的治疗和药物处方。 这些数据还将使研究机构和商业企业能够开发药物,并通过缩短临床试验来加快药物的上市速度。 这个I-Corps项目基于一个基于云的可搜索数据目录的开发,该目录包含来自地理上不同人群的患者基因组,表型和临床数据以及可以分析数据的研究环境。使用来自地理上不同的患者人群的患者数据的能力将允许以高精度确定患者特异性治疗的能力,不仅适用于具有北方欧洲背景的患者,而且适用于任何地方的患者。学术和商业机构将能够通过分析来自不同地理区域的患者数据来改善他们的研究并加快结果,以便在几个小时或几天内回答目前需要数年时间的问题。它将允许商业机构加快治疗研究和简化临床试验。其结果将是更多的药物在更短的时间内以更少的钱通过临床试验治疗更多的疾病。患者数据集还将允许商业机构使用来自不同地理位置的遗传分析来发现患有罕见疾病的患者,而不是目前基于医生确定的预后进行外推的做法。该奖项反映了NSF的法定使命,并通过使用基金会的知识价值和更广泛的影响审查标准进行评估,被认为值得支持。

项目成果

期刊论文数量(0)
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Julian Whitelegge其他文献

emIn situ/em insights into antibody-mediated neutralization of a pre-fusion Junin virus glycoprotein complex
关于抗体介导的融合前胡宁病毒糖蛋白复合物中和作用的原位见解
  • DOI:
    10.1016/j.celrep.2025.115971
  • 发表时间:
    2025-07-22
  • 期刊:
  • 影响因子:
    6.900
  • 作者:
    Lily J. Taylor;Michael R. Sawaya;Jonna B. Westover;Chenyi Wang;Frederick Jimenez;Aldo J. Muñoz;Julian Whitelegge;Brian B. Gowen;Gustavo F. Helguera;Roger Castells-Graells;Jose A. Rodriguez
  • 通讯作者:
    Jose A. Rodriguez
Proinflammatory macrophages release CXCL5 to regulate T cell function and limit effects of αPD-1 in steatosis-driven liver cancer
促炎巨噬细胞释放CXCL5以调节T细胞功能,并限制αPD - 1在脂肪变性驱动的肝癌中的作用
  • DOI:
    10.1016/j.jhepr.2025.101385
  • 发表时间:
    2025-06-01
  • 期刊:
  • 影响因子:
    7.500
  • 作者:
    Taojian Tu;Handan Hong;Diala Alhousari;Lina He;Mario Alba;Yiwei Gu;Brittney Hua;Phillip Nguyen;Qi Tang;Tianyi Xia;Karam Ashouri;Anastasia Martynova;Christina Nakhoul;Whitaker Cohn;Genshu Wang;Geyang Xu;Zhang-Xu Liu;Curtis Okamoto;Enrique Cadenas;Julian Whitelegge;Bangyan L. Stiles
  • 通讯作者:
    Bangyan L. Stiles
Components of <em>E. Coli</em> Energy-Transducing Complexes, ExbB and TolQ, Display Ion Channels
  • DOI:
    10.1016/j.bpj.2009.12.2931
  • 发表时间:
    2010-01-01
  • 期刊:
  • 影响因子:
  • 作者:
    Stanislav D. Zakharov;Herve Celia;Kirill A. Datsenko;Monica Santamaria;Julian Whitelegge;Roland Lloubes;William A. Cramer
  • 通讯作者:
    William A. Cramer
Molecular Conformation and Topography of a Synaptic Lipo-Peptide in Simulated Synaptosomal Membrane Lipids
  • DOI:
    10.1016/j.bpj.2017.11.3320
  • 发表时间:
    2018-02-02
  • 期刊:
  • 影响因子:
  • 作者:
    Julian Whitelegge;Piotr Ruchala;Alan Waring;Cameron Gundersen
  • 通讯作者:
    Cameron Gundersen
324 ER Stress, Irreversible Oxidation of Redox Chaperones and Protein Aggregate Formation in Alcoholic Pancreatitis
  • DOI:
    10.1016/s0016-5085(13)60248-6
  • 发表时间:
    2013-05-01
  • 期刊:
  • 影响因子:
  • 作者:
    Richard T. Waldron;Andreas Gerloff;Payam Javaherizadeh;Julian Whitelegge;Kym Faull;Stephen J. Pandol;Aurelia Lugea
  • 通讯作者:
    Aurelia Lugea

Julian Whitelegge的其他文献

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