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Intelligent patient profiling for diagnosis, staging and treatment selection in colon cancer

机译:结肠癌诊断,分期和治疗选择的智能患者分析

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The selection of a personalized treatment plan for a patient with cancer can be of critical importance for his health or even survival. A Decision Support Platform that can associate the patient clinical situation with the patient DNA Single Nucleotide Polymorphisms (SNPs) can provide the oncologist with a better understanding of the personalized conditions of every single patient. In this paper we present the MATCH plarform which performs data integration between medicine and molecular biology, by developing a framework where, clinical and genomic features are appropriately combined in order to handle colon cancer diseases. The core of the platform is based on clustering techniques which provide profiles of patients with similar clinical features and genetic predispositions to cancer. The patients which share the same profile should probably have similar treatment plan and follow up. Through the integration of the clinical and genetic data of a patient, real time conclusions can be drawn for his early diagnosis, staging and more effective colon cancer treatment. Intelligent components are designed and developed which identify single nucleotide polymorphisms (SNPs) from the gene sequences and combine them with the clinical situation of the patient. The produced clinico-genomic profiles are used as a decision support tool for newly sequenced patients.
机译:对患有癌症的患者的个性化治疗计划的选择对于他的健康甚至生存可能是至关重要的。可以将患者临床状况与患者DNA单一核苷酸多态性(SNP)联系起来的决策支持平台可以提供更好地了解每位患者的个性化条件。在本文中,我们通过开发框架,通过开发适当组合临床和基因组特征以处理结肠癌疾病的框架来进行医学和分子生物学之间进行数据集成的匹配奖项。该平台的核心基于聚类技术,提供患者患者的型材和癌症的遗传易感性。分享相同外形的患者可能有类似的治疗计划并跟进。通过临床和遗传数据的临床和遗传数据,可以采取实时结论,用于他的早期诊断,分期和更有效的结肠癌治疗。设计和开发智能组分,其从基因序列中鉴定单个核苷酸多态性(SNP),并将它们与患者的临床状况组成。所生产的临床基因组型材用作新序列患者的决策支持工具。

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