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BIGDATA: Collaborative Research: IA: Big Imaging-Omics Data Mining Framework for Precision Medicine

BIGDATA: Collaborative Research: IA: Big Imaging-Omics Data Mining Framework for Precision Medicine
BIGDATA:协作研究:IA:精准医学大影像组学数据挖掘框架
批准号:
1852606
负责人:
Heng Huang
金额:
$125.34万
依托单位:
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-09-01 至 2022-09-30

项目摘要

项目成果

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中文摘要
翻译
本提案的研究目标是解决基于成像组学的精准医学中创新大数据应用的计算挑战。高通量成像(如组织病理学图像)和多组学(如DNA序列、RNA表达、甲基化等)技术的最新进展为利用定量方法探索组织学、分子事件和临床结果之间的关系创造了新的机会。然而,这些成像组学数据的空前规模和复杂性提出了关键的计算瓶颈,需要新的概念和支持工具。该项目构建了一个新的计算框架,将新颖的大数据挖掘算法与云和高性能计算策略集成在一起,以揭示组织病理学图像、多组学和表型结果之间的复杂关系。该项目具有创新性,不仅对促进新的大数据挖掘技术的发展至关重要,而且对解决成像组学和许多其他生物医学应用中的新兴科学问题也至关重要。开发的方法和工具有望影响其他癌症基因组学研究,并使研究癌症医学的研究人员能够有效地验证他们的科学假设。这个项目促进了新的教育工具的开发,以加强一些现有的课程。德克萨斯大学阿灵顿分校是一所少数族裔服务机构,拥有大量西班牙裔和黑人美国人。该项目让少数民族学生和服务不足的人群参与研究活动,让他们更好地接触前沿科学研究。为了解决大成像组学数据挖掘中的关键和挑战问题,本项目探索了以下研究任务:首先,开发了大规模非凸稀疏学习模型,用于从大组织病理学图像中识别与结果相关的表型特征。其次,利用生物领域知识指导稀疏学习模型揭示复杂性状的分子基础;第三,设计数据集成模型,整合来自多个来源的成像组学数据,发现异质生物标志物。第四,探索贝叶斯学习模型来预测纵向癌症预后。第五,开发了云计算和高性能计算策略,以支持大成像组学数据挖掘,例如优化异构硬件(如GPU和NUMA多核处理器)上的各种数据挖掘工作负载,以充分释放数据中心硬件的潜力。将大数据挖掘算法与云和高性能计算集成到成像组学中是一种创新,为精准医学的系统生物学带来了巨大的希望。
英文摘要
The research objective of this proposal is to address the computational challenges in an innovative BIGDATA application on imaging-omics based precision medicine. Recent advances in high-throughput imaging (such as histopathology image) and multi-omics (such as DNA sequence, RNA expression, methylation, etc.) technologies created new opportunities for exploring relationships between histology, molecular events, and clinical outcomes using quantitative methods. However, the unprecedented scale and complexity of these imaging-omic data have presented critical computational bottlenecks requiring new concepts and enabling tools. This project builds a new computational framework to integrate novel big data mining algorithms with cloud and high-performance computing strategies for revealing complex relationships between histopathology images, multi-omics, and phenotypic outcomes. This project is innovative and crucial not only to facilitating the development of new big data mining techniques, but also to addressing emerging scientific questions in imaging-omics and many other biomedical applications. The developed methods and tools are expected to impact other cancer genomics research and enable investigators working on cancer medicine to effectively test their scientific hypothesis. This project facilitates the development of novel educational tools to enhance several current courses. University of Texas at Arlington is a minority-serving institution and has large population of Hispanic and Black Americans. This project engages the minority students and under-served populations in research activities to give them a better exposure to cutting-edge science research.To solve the key and challenge problems in big imaging-omics data mining, this project explores the following research tasks. First, the large-scale non-convex sparse learning models are developed for identifying outcome-relevant phenotypic traits from big histopathology images. Second, the biological domain knowledge is utilized to guide the sparse learning models to uncover the molecular bases of complex traits. Third, the data integration models are designed to integrate imaging-omics data from multiple sources and discover the heterogeneous biomarkers. Fourth, the Baysian learning model is explored to predict longitudinal cancer outcomes. Fifth, the cloud computing and high-performance computing strategies are developed to support the big imaging-omics data mining, such as optimizations for various data mining workloads on heterogeneous hardware (e.g. GPU and NUMA multicore processors) to fully unlock the potential of data center hardware. It is innovative to integrate big data mining algorithms with cloud and high-performance computing to imaging-omics that hold great promise for a systems biology of the precision medicine.
期刊论文(45)
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会议论文
DOI: --
发表时间: 2019-06
期刊:
影响因子: --
作者: [Hongchang Gao;J. Pei;Heng Huang]
通讯作者: Hongchang Gao;J. Pei;Heng Huang
DOI: 10.1609/aaai.v35i9.16962
发表时间: 2021-05
期刊:
影响因子: --
作者: [Zhouyuan Huo;Bin Gu;Heng Huang]
通讯作者: Zhouyuan Huo;Bin Gu;Heng Huang
DOI: 10.1007/978-3-030-59710-8_62
发表时间: 2020-10
期刊: Micromachines
影响因子: 3.4
作者: [Alireza Ganjdanesh;Kamran Ghasedi;L. Zhan;Weidong (Tom) Cai;Heng Huang]
通讯作者: Alireza Ganjdanesh;Kamran Ghasedi;L. Zhan;Weidong (Tom) Cai;Heng Huang
DOI: 10.48550/arxiv.2302.03825
发表时间: 2023-02
期刊: ArXiv
影响因子: --
作者: [Xidong Wu;Zhengmian Hu;Heng Huang]
通讯作者: Xidong Wu;Zhengmian Hu;Heng Huang
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