TY - JOUR AU - Ge, Ruiquan AU - Feng, Guanwen AU - Jing, Xiaoyang AU - Zhang, Renfeng AU - Wang, Pu AU - Wu, Qing PY - 2020 M3 - Methods TI - EnACP: An Ensemble Learning Model for Identification of Anticancer Peptides JO - Frontiers in Genetics UR - https://www.frontiersin.org/articles/10.3389/fgene.2020.00760 VL - 11 SN - 1664-8021 N2 - As cancer remains one of the main threats of human life, developing efficient cancer treatments is urgent. Anticancer peptides, which could overcome the significant side effects and poor results of traditional cancer treatments, have become a new potential alternative these years. However, identifying anticancer peptides by experimental methods is time consuming and resource consuming, it is of great significance to develop effective computational tools to quickly and accurately identify potential anticancer peptides from amino acid sequences. For most current computational methods, feature representation plays a key role in their final successes. This study proposes a novel fast and accurate approach to identify anticancer peptides using diversified feature representations and ensemble learning method. For the feature representations, the information is encoded from multidimensional feature spaces, including sequence composition, sequence-order, physicochemical properties, etc. In order to better model the potential relationships of peptides, multiple ensemble classifiers, LightGBMs, are applied to detect the different feature sets at first. Then the obtained multiple outputs are used as inputs of the support vector machine classifier, which effectively identifies anticancer peptides. Experimental results on cross validation and independent test sets demonstrate that our method can achieve better or comparable performances compared with other state-of-the-art methods. ER -