Evidence map›Paper›PMID 35571057›Full record

ArticleFrontiers in genetics2022

i2APP: A Two-Step Machine Learning Framework For Antiparasitic Peptides Identification.

Minchao Jiang, Renfeng Zhang, Yixiao Xia, Gangyong Jia, Yuyu Yin, Pu Wang, Jian Wu, Ruiquan Ge

Abstract read
In one paragraph

Article in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Minchao JiangSchool of Computer Science and Technology, Hangzhou Dianzi University, Hangzhou, China.
Renfeng ZhangShandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.
Yixiao XiaSchool of Computer Science and Technology, Hangzhou Dianzi University, Hangzhou, China.
Gangyong JiaSchool of Computer Science and Technology, Hangzhou Dianzi University, Hangzhou, China.
Yuyu YinSchool of Computer Science and Technology, Hangzhou Dianzi University, Hangzhou, China.
Pu WangComputer School, Hubei University of Arts and Science, Xiangyang, China.
Jian WuMyGenostics Inc., Beijing, China.
Ruiquan GeSchool of Computer Science and Technology, Hangzhou Dianzi University, Hangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parasites can cause enormous damage to their hosts. Studies have shown that antiparasitic peptides can inhibit the growth and development of parasites and even kill them. Because traditional biological methods to determine the activity of antiparasitic peptides are time-consuming and costly, a method for large-scale prediction of antiparasitic peptides is urgently needed. We propose a computational approach called i2APP that can efficiently identify APPs using a two-step machine learning (ML) framework. First, in order to solve the imbalance of positive and negative samples in the training set, a random under sampling method is used to generate a balanced training data set. Then, the physical and chemical features and terminus-based features are extracted, and the first classification is performed by Light Gradient Boosting Machine (LGBM) and Support Vector Machine (SVM) to obtain 264-dimensional higher level features. These features are selected by Maximal Information Coefficient (MIC) and the features with the big MIC values are retained. Finally, the SVM algorithm is used for the second classification in the optimized feature space. Thus the prediction model i2APP is fully constructed. On independent datasets, the accuracy and AUC of i2APP are 0.913 and 0.935, respectively, which are better than the state-of-arts methods. The key idea of the proposed method is that multi-level features are extracted from peptide sequences and the higher-level features can distinguish well the APPs and non-APPs.

Indexed as

antiparasitic peptidesfeature representationfeature selectionmaximum information coefficientT-distributed stochastic neighbor embedding

Identifiers

PMID35571057
PMCPMC9091563

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