RUN-ONCO:一个高度可扩展的癌症精准医疗软件平台

Neda Peyrone, D. Wichadakul
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引用次数: 2

摘要

精准医学是一种通过遗传学来个性化疾病识别和医疗护理决策的策略。快速发展的组学技术,例如DNA和RNA测序,可以揭示患者肿瘤中的特定基因突变或药物反应的基因表达谱,帮助肿瘤学家根据个体患者的遗传学找到有效的治疗方法。因此,除了临床记录外,组学数据对个性化诊断和治疗至关重要。本文提出了一个基于网络的癌症精准医疗独立软件平台RUN-ONCO,旨在帮助肿瘤学家和研究人员轻松高效地管理和利用现有的临床和组学数据。该平台允许管理临床记录、生物标本和组学数据,并支持与公共数据库(如STRING和OncoKB)一起进行各种综合数据分析。随着各种组学数据分析方法的发布数量的增加,以及用于数据可视化的大量javascript库的可用性,RUN-ONCO也被设计成具有高度可扩展性,可以使用可视化和分析方法的插件。RUN-ONCO的演示版本可在http://cucpbioinfo.cp.eng.chula.ac.th:6002上在线获得,本地部署的源代码可在https://gitlab.com/peyrone/run-onco上获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RUN-ONCO: A Highly Extensible Software Platform for Cancer Precision Medicine
Precision medicine is a strategy to personalize disease identification and medical care decisions through genetics. The rapid development of -omics technologies e.g., DNA and RNA sequencing, which reveal specific gene mutations in a patient's tumor or profiling of gene expressions for drug responses helps oncologists find effective treatments for individual patients based on their genetics. Hence, besides the clinical records, -omics data become essential for personalized diagnosis and treatments. In this paper, a web-based standalone software platform for cancer precision medicine, called RUN-ONCO, is proposed aiming to help oncologists and researchers manage and make use of the available clinical and -omics data easily and efficiently. The platform allows the management of clinical records, biospecimens, and -omics data and enables various integrative data analyses together with public databases such as STRING and OncoKB. With the increasing number of published methods for various -omics data analyses together with the availability of numerous javascript libraries for data visualization, RUN-ONCO has also been designed to be highly extensible with plugins for both visualizations and analysis methods. A demo version of RUN-ONCO is available online at http://cucpbioinfo.cp.eng.chula.ac.th:6002 and the source code for local deployment is at https://gitlab.com/peyrone/run-onco.
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