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A Novel Hybrid Sequence-Based Model for Identifying Anticancer Peptides

机译:基于杂交序列的新型抗癌肽鉴定模型

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Cancer is a serious health issue worldwide. Traditional treatment methods focus on killing cancer cells by using anticancer drugs or radiation therapy, but the cost of these methods is quite high, and in addition there are side effects. With the discovery of anticancer peptides, great progress has been made in cancer treatment. For the purpose of prompting the application of anticancer peptides in cancer treatment, it is necessary to use computational methods to identify anticancer peptides (ACPs). In this paper, we propose a sequence-based model for identifying ACPs (SAP). In our proposed SAP, the peptide is represented by 400D features or 400D features with g-gap dipeptide features, and then the unrelated features are pruned using the maximum relevance-maximum distance method. The experimental results demonstrate that our model performs better than some existing methods. Furthermore, our model has also been extended to other classifiers, and the performance is stable compared with some state-of-the-art works.
机译:癌症是全世界严重的健康问题。传统的治疗方法侧重于通过使用抗癌药或放射疗法杀死癌细胞,但是这些方法的成本相当高,并且还存在副作用。随着抗癌肽的发现,在癌症治疗中已取得了很大的进步。为了促进抗癌肽在癌症治疗中的应用,有必要使用计算方法来鉴定抗癌肽(ACP)。在本文中,我们提出了一种用于识别ACP(SAP)的基于序列的模型。在我们提出的SAP中,该肽由具有g间隙二肽特征的400D特征或400D特征表示,然后使用最大相关性-最大距离方法对不相关的特征进行修剪。实验结果表明,我们的模型比某些现有方法具有更好的性能。此外,我们的模型也已扩展到其他分类器,并且与某些最新作品相比,性能稳定。

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