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A Data Aggregation Framework for Cancer Subtype Discovery

机译:癌症亚型发现的数据聚合框架

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Personalized genomic medicine aims to revolutionize healthcare by applying our growing understanding of the molecular basis of disease for effective diagnosis and personalized therapy. Computational research in this arena has major challenges such as handling large volume of highly heterogeneous data sets. To extract knowledge, researchers must integrate data from several sources and efficiently query these large and diverse data sets. This presents daunting informatics challenges such as suitable data representation for computational inference (knowledge representation), linking heterogeneous data sets (data integration) and keeping track of the source of the data to be aggregated. Many of these challenges can be categorized as data integration problems. In this paper, we present relevant methodologies from the field of data integration as potential solution for such challenges encountered by computational biologist while handling diversified data. The work presented in the paper represents the first crucial step towards identifying cancer biomarkers leading to cancer pathways signatures and personalized medicine.
机译:个性化的基因组医学旨在通过应用我们对有效诊断和个性化治疗的分子基础的越来越多的理解来彻底改变医疗保健。该舞台的计算研究具有重大挑战,例如处理大量高度异构数据集。为了提取知识,研究人员必须将数据从多种来源集成并有效地查询这些大型和不同的数据集。这提出了令人生畏的信息学挑战,例如用于计算推理的合适数据表示(知识表示),链接异构数据集(数据集成)并跟踪要聚合的数据源。许多这些挑战可以作为数据集成问题进行分类。在本文中,我们将数据集成领域的相关方法作为计算生物学家在处理多样化数据时遇到的潜在解决方案。本文所呈现的工作代表了旨在识别癌症生物标志物导致癌症途径和个性化医学的第一个至关重要的步骤。

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