递归神经网络线性b表位预测器:BIRUNI

A. Abidi
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引用次数: 0

摘要

抗原表位在多肽疫苗的开发、疾病的诊断和过敏研究中起着至关重要的作用,用于表征抗原表位的实验方法耗时且需要大量资源。有许多在线表位预测工具可用,可以帮助科学家在候选肽短列表。为了预测抗原序列中的b细胞表位,Jordan递归神经网络(BIRUNI)被发现是成功的。为了训练和测试神经网络,从IEDB数据库中检索了262.583个B表位。99.9%的表位长度在6-25个氨基酸之间。对于每一个长度,由11个专家组成的循环神经网络委员会都要接受训练。为了训练这些专家,除了表位之外,还需要非表位。非表位是由相同长度的氨基酸随机序列通过过滤过程产生的。为了区分表位和非表位,11位专家的投票以多数投票的方式汇总。总体准确率达到97.23%。然后利用这些专家来预测恶性疟原虫、人类脊髓灰质炎病毒沙宾株、脑膜炎、间日疟原虫和结核分枝杆菌这五种抗原的线性倍人猿。BIRUNU的成功与5种在线预测工具ABCPRED、BCPRED、K&T、BEPIPRED和AAP进行了比较。可以看出,BIRUNI的平均表现优于所有这些。
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A Recurrent Neural Network Linear B-Epitope Predictor: BIRUNI
Experimental methods used for characterizing epitopes that play a vital role in the development of peptide vaccines, in diagnosis of diseases, and also for allergy research are time consuming and need huge resources. There are many online epitope prediction tools are available that can help scientists in short listing the candidate peptides. To predict B-cell epitopes in an antigenic sequence, Jordan recurrent neural network (BIRUNI) is found to besuccessful. To train and test neural networks, 262.583 B epitopes are retrieved from IEDB database. 99.9% of these epitopes have lengths in the interval 6-25 amino acids. For each of these lengths, committees of 11 expert recurrent neural networks are trained. To train these experts alongside epitopes, non-epitopes are needed. Non-epitopes are created as random sequences of amino acids of the same length followed by a filtering process. To distinguish epitopes and non-epitopes, the votes of eleven experts are aggregated by majority vote. An overall accuracy of 97.23% is achieved. Then these experts are used to predict the Linear Bepitopes of five antigens, Plasmodium Falciparum, Human Polio Virus Sabin Strain, Meningitis, Plasmodium Vivax and Mycobacterium Tuberculosis. The success of BIRUNU is compared with the five online prediction tools ABCPRED, BCPRED, K&T, BEPIPRED, and AAP.It is seen that BIRUNI outperforms all of them in the average.
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