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Logistic Weighted Profile-Based Bi-Random Walk for Exploring MiRNA-Disease Associations

机译:基于物流加权曲线的双随机散步,用于探索miRNA-疾病协会

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MicroRNAs(miRNAs)exert an enormous influence on cell differentiation,biological development and the onset of diseases.Because predicting potential miRNA-disease associations(MDAs)by biological experiments usually requires considerable time and money,a growing number of researchers are working on developing computational methods to predict MDAs.High accuracy is critical for prediction.To date,many algorithms have been proposed to infer novel MDAs.However,they may still have some drawbacks.In this paper,a logistic weighted profile-based bi-random walk method(LWBRW)is designed to infer potential MDAs based on known MDAs.In this method,three networks(i.e.,a miRNA functional similarity network,a disease semantic similarity network and a known MDA network)are constructed first.In the process of building the miRNA network and the disease network,Gaussian interaction profile(GIP)kernel is computed to increase the kernel similarities,and the logistic function is used to extract valuable information and protect known MDAs.Next,the known MDA matrix is preprocessed by the weighted K-nearest known neighbours(WKNKN)method to reduce the number of false negatives.Then,the LWBRW method is applied to infer novel MDAs by bi-randomly walking on the miRNA network and the disease network.Finally,the predictive ability of the LWBRW method is confirmed by the average AUC of 0.9393(0.0061)in 5-fold cross-validation(CV)and the AUC value of 0.9763 in leave-one-out cross-validation(LOOCV).In addition,case studies also show the outstanding ability of the LWBRW method to explore potential MDAs.
机译:MicroRNAS(miRNA)对细胞分化,生物发育和疾病发病产生了巨大影响。因为通过生物实验预测潜在的miRNA - 疾病协会(MDA)通常需要相当多的时间和金钱,越来越多的研究人员正在努力开发计算预测MDAS的方法。对于预测,高精度至关重要。迄今为止,已经提出了许多算法来推断出新的MDAS。然而,它们仍然可以具有一些缺点。本文,基于物流加权曲线的双随机步行方法( LWBRW)首先构建了基于已知MDA的潜在MDAS。在该方法中,三个网络(即,MiRNA功能相似性网络,疾病语义相似性网络和已知的MDA网络)。在构建miRNA的过程中构建网络和疾病网络,计算高斯交互配置文件(GIP)内核以增加内核相似之处,并且逻辑函数用于提取有价值的信息已知的MDAS.next,已知的MDA矩阵被加权K-最近已知的邻居(WKNKN)方法预处理,以减少假底片的数量。该方法通过双随机行走应用LWBRW方法以推断新颖的MDA在miRNA网络和疾病网络上。最后,LWBRW方法的预测能力通过0.9393(0.0061)的平均AUC在5倍交叉验证(CV)和0.9763的休假中的AUC值确认为0.9763外交叉验证(LOOCV)。此外,案例研究还表明了LWBRW方法探索潜在MDA的优势。

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