Distance based knowledge retrieval through rule mining for complex biomarker recognition from tri-omics profiles

Saurav Mallik, Zhongming Zhao
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引用次数: 2

Abstract

Biomarker discovery from complex biomedical data has become an important topic to unveil the significant new disease signals for disease diagnosis and treatment during past two decades. The earlier methods were proposed on a single genomic profile, and most of them utilize a single minimum support/confidence/lift cutoff. To overcome these shortcomings, here, we developed a framework for identifying complex markers using shortest distance based rule mining from the tri-omics profiles (gene expression, methylation and protein-protein interaction). We applied our method to a high-grade soft-tissue sarcomas multi-omics dataset. The novel markers were {GRB2-, STAT3-}('-' and '+' denote decreased and increased gene activities, respectively), {STAT3+, TP53-, MAPK3+} and {STAT3+, FYN+, MAPK3+}. We showed the superiority of our method vs. others, as it generates fewer rules and lower mean of the shortest distance than others. Moreover, our method is useful to extract complex markers from tri-omics profiles for the complex disease.
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基于规则挖掘的基于距离的知识检索,用于三组学图谱中复杂生物标志物的识别
近二十年来,从复杂的生物医学数据中发现生物标志物已成为揭示疾病诊断和治疗的重要新疾病信号的重要课题。早期的方法是针对单个基因组图谱提出的,大多数方法使用单个最小支持/置信度/提升截止。为了克服这些缺点,我们开发了一个框架,利用基于最短距离的规则挖掘从三组学图谱(基因表达、甲基化和蛋白质-蛋白质相互作用)中识别复杂标记。我们将我们的方法应用于高级别软组织肉瘤多组学数据集。新标记为{GRB2-, STAT3-}(“-”和“+”分别表示基因活性降低和增加),{STAT3+, TP53-, MAPK3+}和{STAT3+, FYN+, MAPK3+}。我们展示了我们的方法相对于其他方法的优越性,因为它生成的规则更少,最短距离的平均值更低。此外,我们的方法可用于从复杂疾病的三组学图谱中提取复杂标记。
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