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Predicting miRNA-disease associations using a hybrid feature representation in the heterogeneous network

机译:使用异构网络中的混合特征表示预测miRNA疾病关联

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摘要

MicroRNAs(miRNAs) are a kind of small single-stranded endogenous non-coding RNAs with a length about 22 nucleotides, which play an important role in regulating the gene expression during the post-transcriptional level [1, 2]. Many studies have shown that the dysregulation of miRNAs is involved in multiple human diseases like cancers [3], cardiovascular diseases [4] and Alzheimer’s diseases [5] etc., and the prediction of miRNAs-diseases associations is crucial to understand the diseases pathogenesis [6]. Furthermore, George Adrian, et al. found that the miR15 and miR16 are deleted in a lot B cell chronic lymphocytic leukemias (B-CLL) [7], T. Sredni et al. demonstrated that miR-129 and miR-25 express abnormally in all pediatric brain tumor types [8]. Besides, Jun Lu et al. successfully classified poorly differentiated tumours using miRNA expression profiles [9], which demonstrated the potential of miRNAs as biomarkers. Therefore, Predicting miRNA-disease associations is very meaningful. However, a lot of miRNA-disease associations remain unknown and experimental approaches for predicting the associations are time-consuming and expensive. Therefore, a lot computational methods have been developed to predict the miRNA-disease associations.
机译:MicroRNAs(miRNA)是一种小的单链内源性非编码RNA,其长度约为22个核苷酸,这在调节转录后水平[1,2]期间的基因表达起着重要作用。许多研究表明,miRNA的失调参与了癌症的多种人类疾病[3],心血管疾病[4]和阿尔茨海默氏病[5]等,并且对患有疾病发病机制至关重要的米兰疾病关联至关重要[6]。此外,George Adrian等人。发现MIR15和MIR16在批次B细胞慢性淋巴细胞白血病(B-CLL)[7],T.Sredni等人中删除。证明MIR-129和MIR-25在所有儿科脑肿瘤类型中异常表达[8]。此外,Jun Lu等。使用miRNA表达谱(MiRNA表达谱分类差异差异差异差异,表明MIRNAS作为生物标志物的潜力。因此,预测miRNA疾病关联非常有意义。然而,许多miRNA疾病关联仍然是未知的并且预测协会的实验方法是耗时和昂贵的。因此,已经开发了许多计算方法来预测miRNA疾病关联。

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