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AN APPLICATION OF ASSOCIATION RULE MINING TO HLA-A*0201 EPITOPE PREDICTION

机译:关联规则挖掘对HLA-A * 0201表位预测的应用

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This paper presents a novel approach to epitope prediction based on the clustering of known T-cell epitopes for a given MHC class I allele (HLA-A*0201). A combination of association rules (ARs) and sequence-structure patterns (SSPs) was used to do the clustering of training set epitopes from the Antijen database. A regression model was then built from each cluster and a peptide from the test set was declared to be an epitope only if one or more of the models gave a positive prediction. The sensitivity (TP/TP+FN) of the AR/SSP regression models approach was higher than that of a single regression model built on the entire training set, and was also higher than the sensitivity measures for SYFPEITHI, Rankpep, and ProPredl on the same test set.
机译:本文提出了一种基于已知的MHC I类等位基因的已知T细胞表位的聚类对表位预测的新方法(HLA-A * 0201)。关联规则(ARS)和序列结构模式(SSP)的组合用于从Antijen数据库进行训练集表的群集。然后,仅从每个簇中构建回归模型,并且仅当一个或多个模型给出阳性预测时,从测试集中的肽被声明为表位。 AR / SSP回归模型方法的灵敏度(TP / TP + FN)高于整个培训集内置的单一回归模型的灵敏度(TP / TP + FN),也高于Syfpeithi,ScalPep和Propredl的灵敏度措施相同的测试集。

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