Evidence map›Paper›PMID 26020952›Full record

ArticlePloS one2015

Accurate prediction of immunogenic T-cell epitopes from epitope sequences using the genetic algorithm-based ensemble learning.

Wen Zhang, Yanqing Niu, Hua Zou, Longqiang Luo, Qianchao Liu, Weijian Wu

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.5field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 35 citations in OpenAlex.

  1. Deep learning of antibody epitopes using positional permutation vectors.Computational and structural biotechnology journal · 2024
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  12. RFAmyloid: A Web Server for Predicting Amyloid Proteins.International journal of molecular sciences · 2018
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Wen ZhangSchool of Computer, Wuhan University, Wuhan, 430072, China; Research Institute of Shenzhen, Wuhan University, Shenzhen, 518057, China.
Yanqing NiuSchool of Mathematics and Statistics, South-central University for Nationalities, Wuhan, 430074, China.
Hua ZouSchool of Computer, Wuhan University, Wuhan, 430072, China.
Longqiang LuoSchool of Mathematics and Statistics, Wuhan University, Wuhan, 430072, China.
Qianchao LiuSchool of Computer, Wuhan University, Wuhan, 430072, China.
Weijian WuSchool of Computer, Wuhan University, Wuhan, 430072, China.
Wuhan University · CNSouth Central University for Nationalities · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundT-cell epitopes play the important role in T-cell immune response, and they are critical components in the epitope-based vaccine design. Immunogenicity is the ability to trigger an immune response. The accurate prediction of immunogenic T-cell epitopes is significant for designing useful vaccines and understanding the immune system.

methodsIn this paper, we attempt to differentiate immunogenic epitopes from non-immunogenic epitopes based on their primary structures. First of all, we explore a variety of sequence-derived features, and analyze their relationship with epitope immunogenicity. To effectively utilize various features, a genetic algorithm (GA)-based ensemble method is proposed to determine the optimal feature subset and develop the high-accuracy ensemble model. In the GA optimization, a chromosome is to represent a feature subset in the search space. For each feature subset, the selected features are utilized to construct the base predictors, and an ensemble model is developed by taking the average of outputs from base predictors. The objective of GA is to search for the optimal feature subset, which leads to the ensemble model with the best cross validation AUC (area under ROC curve) on the training set.

resultsTwo datasets named 'IMMA2' and 'PAAQD' are adopted as the benchmark datasets. Compared with the state-of-the-art methods POPI, POPISK, PAAQD and our previous method, the GA-based ensemble method produces much better performances, achieving the AUC score of 0.846 on IMMA2 dataset and the AUC score of 0.829 on PAAQD dataset. The statistical analysis demonstrates the performance improvements of GA-based ensemble method are statistically significant.

conclusionsThe proposed method is a promising tool for predicting the immunogenic epitopes. The source codes and datasets are available in S1 File.

Indexed as

AlgorithmsModels, GeneticModels, ImmunologicalAmino Acid SequenceComputer SimulationDatasets as TopicEpitopes, T-LymphocyteHumansMolecular Sequence DataROC CurveT-LymphocytesVaccines, SyntheticEpitopes, T-LymphocyteVaccines, Synthetic

Identifiers

PMID26020952
PMCPMC4447411
OpenAlexW1559579542

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.