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OncoRep: an n-of-1 reporting tool to support genome-guided treatment for breast cancer patients using RNA-sequencing

机译:OncoRep:n-of-1报告工具,支持使用RNA测序技术对乳腺癌患者进行基因组指导治疗

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Background Breast cancer comprises multiple tumor entities associated with different biological features and clinical behaviors, making individualized medicine a powerful tool to bring the right drug to the right patient. Next generation sequencing of RNA (RNA-Seq) is a suitable method to detect targets for individualized treatment. Challenges that arise are i) preprocessing and analyzing RNA-Seq data in the n-of-1 setting, ii) extracting clinically relevant and actionable targets from complex data, iii) integrating drug databases, and iv) reporting results to clinicians in a timely and understandable manner. Results To address these challenges, we present OncoRep, an RNA-Seq based n-of-1 reporting tool for breast cancer patients. It reports molecular classification, altered genes and pathways, gene fusions, clinically actionable mutations and drug recommendations. It visualizes the data in an approachable html-based interactive report and a PDF clinical report, providing the clinician and tumor board with a tool to guide the treatment decision making process. Conclusions OncoRep is free and open-source ( https://?bitbucket.?org/?sulab/?oncorep/? ), thereby offering a platform for future development and innovation by the community.
机译:背景技术乳腺癌包括与不同生物学特征和临床行为相关的多个肿瘤实体,这使得个性化药物成为将正确的药物带给正确的患者的有力工具。下一代RNA测序(RNA-Seq)是检测目标个体化治疗的合适方法。出现的挑战是:i)在n-of-1环境中预处理和分析RNA-Seq数据,ii)从复杂数据中提取临床相关且可操作的靶标,iii)整合药物数据库,iv)及时向临床医生报告结果和可以理解的方式。结果为了解决这些挑战,我们提出了OncoRep,一种基于RNA-Seq的n-of-1报告工具,用于乳腺癌患者。它报告了分子分类,改变的基因和途径,基因融合,临床上可行的突变以及药物推荐。它通过基于HTML的交互式报告和PDF临床报告将数据可视化,为临床医生和肿瘤委员会提供了指导治疗决策过程的工具。结论OncoRep是免费和开源的(https://?bitbucket。?org /?sulab /?oncorep /?),从而为社区的未来发展和创新提供了一个平台。

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