通过云基础设施重构为罕见疾病提供精准医疗。

Hui Li, Jinlian Wang, Hongfang Liu
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引用次数: 0

摘要

大约每11个美国人中就有1人患有罕见病,但由于临床证据有限、认识不足和缺乏明确的治疗方法,对罕见病的诊断仍然具有挑战性。我们的项目旨在通过开发综合信息学框架,利用数据挖掘、语义网技术、深度学习和基于图的嵌入技术,加速罕见病的诊断。然而,我们的本地计算基础设施在可伸缩性、维护和协作方面面临着重大挑战。本研究的重点是开发和评估基于云的计算基础设施,以应对这些挑战。通过迁移到一个可扩展的、安全的、协作的云环境,我们的目标是增强数据集成,支持先进的鉴别诊断预测建模,促进研究成果向利益相关者、研究界和公众的广泛传播,并提出了一个可靠的、标准化的工作流程,旨在确保最小的中断和维护现有研究项目的数据完整性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Empowering Precision Medicine for Rare Diseases through Cloud Infrastructure Refactoring.

Rare diseases affect approximately 1 in 11 Americans, yet their diagnosis remains challenging due to limited clinical evidence, low awareness, and lack of definitive treatments. Our project aims to accelerate rare disease diagnosis by developing a comprehensive informatics framework leveraging data mining, semantic web technologies, deep learning, and graph-based embedding techniques. However, our on-premises computational infrastructure faces significant challenges in scalability, maintenance, and collaboration. This study focuses on developing and evaluating a cloud-based computing infrastructure to address these challenges. By migrating to a scalable, secure, and collaborative cloud environment, we aim to enhance data integration, support advanced predictive modeling for differential diagnoses, and facilitate widespread dissemination of research findings to stakeholders, the research community, and the public and also proposed a facilitated through a reliable, standardized workflow designed to ensure minimal disruption and maintain data integrity for existing research project.

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