Dataset Information

Evaluating and Improving Automatic Sleep Spindle Detection by Using Multi-Objective Evolutionary Algorithms.

ABSTRACT: Sleep spindles are brief bursts of brain activity in the sigma frequency range (11-16 Hz) measured by electroencephalography (EEG) mostly during non-rapid eye movement (NREM) stage 2 sleep. These oscillations are of great biological and clinical interests because they potentially play an important role in identifying and characterizing the processes of various neurological disorders. Conventionally, sleep spindles are identified by expert sleep clinicians via visual inspection of EEG signals. The process is laborious and the results are inconsistent among different experts. To resolve the problem, numerous computerized methods have been developed to automate the process of sleep spindle identification. Still, the performance of these automated sleep spindle detection methods varies inconsistently from study to study. There are two reasons: (1) the lack of common benchmark databases, and (2) the lack of commonly accepted evaluation metrics. In this study, we focus on tackling the second problem by proposing to evaluate the performance of a spindle detector in a multi-objective optimization context and hypothesize that using the resultant Pareto fronts for deriving evaluation metrics will improve automatic sleep spindle detection. We use a popular multi-objective evolutionary algorithm (MOEA), the Strength Pareto Evolutionary Algorithm (SPEA2), to optimize six existing frequency-based sleep spindle detection algorithms. They include three Fourier, one continuous wavelet transform (CWT), and two Hilbert-Huang transform (HHT) based algorithms. We also explore three hybrid approaches. Trained and tested on open-access DREAMS and MASS databases, two new hybrid methods of combining Fourier with HHT algorithms show significant performance improvement with F₁-scores of 0.726-0.737.

SUBMITTER: Liu MY

PROVIDER: S-EPMC5435763 | biostudies-literature | 2017

REPOSITORIES: biostudies-literature

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Publications

Evaluating and Improving Automatic Sleep Spindle Detection by Using Multi-Objective Evolutionary Algorithms.

Liu Min-Yin MY Huang Adam A Huang Norden E NE

Frontiers in human neuroscience 20170518

Sleep spindles are brief bursts of brain activity in the sigma frequency range (11-16 Hz) measured by electroencephalography (EEG) mostly during non-rapid eye movement (NREM) stage 2 sleep. These oscillations are of great biological and clinical interests because they potentially play an important role in identifying and characterizing the processes of various neurological disorders. Conventionally, sleep spindles are identified by expert sleep clinicians via visual inspection of EEG signals. Th ...[more]

PMID: 28572762

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Project description:BackgroundPeptides binding to Major Histocompatibility Complex (MHC) class II molecules are crucial for initiation and regulation of immune responses. Predicting peptides that bind to a specific MHC molecule plays an important role in determining potential candidates for vaccines. The binding groove in class II MHC is open at both ends, allowing peptides longer than 9-mer to bind. Finding the consensus motif facilitating the binding of peptides to a MHC class II molecule is difficult because of different lengths of binding peptides and varying location of 9-mer binding core. The level of difficulty increases when the molecule is promiscuous and binds to a large number of low affinity peptides. In this paper, we propose two approaches using multi-objective evolutionary algorithms (MOEA) for predicting peptides binding to MHC class II molecules. One uses the information from both binders and non-binders for self-discovery of motifs. The other, in addition, uses information from experimentally determined motifs for guided-discovery of motifs.ResultsThe proposed methods are intended for finding peptides binding to MHC class II I-Ag7 molecule - a promiscuous binder to a large number of low affinity peptides. Cross-validation results across experiments on two motifs derived for I-Ag7 datasets demonstrate better generalization abilities and accuracies of the present method over earlier approaches. Further, the proposed method was validated and compared on two publicly available benchmark datasets: (1) an ensemble of qualitative HLA-DRB1*0401 peptide data obtained from five different sources, and (2) quantitative peptide data obtained for sixteen different alleles comprising of three mouse alleles and thirteen HLA alleles. The proposed method outperformed earlier methods on most datasets, indicating that it is well suited for finding peptides binding to MHC class II molecules.ConclusionWe present two MOEA-based algorithms for finding motifs, one for self-discovery and the other for guided-discovery by experimentally determined motifs, and thereby predicting binding peptides to I-Ag7 molecule. Our experiments show that the proposed MOEA-based algorithms are better than earlier methods in predicting binding sites not only on I-Ag7 but also on most alleles of class II MHC benchmark datasets. This shows that our methods could be applicable to find binding motifs in a wide range of alleles.

Project description:BackgroundStudies on genome-wide associations help to determine the cause of many genetic diseases. Genome-wide associations typically focus on associations between single-nucleotide polymorphisms (SNPs). Genotyping every SNP in a chromosomal region for identifying genetic variation is computationally very expensive. A representative subset of SNPs, called tag SNPs, can be used to identify genetic variation. Small tag SNPs save the computation time of genotyping platform, however, there could be missing data or genotyping errors in small tag SNPs. This study aims to solve Tag SNPs selection problem using many-objective evolutionary algorithms.MethodsTag SNPs selection can be viewed as an optimization problem with some trade-offs between objectives, e.g. minimizing the number of tag SNPs and maximizing tolerance for missing data. In this study, the tag SNPs selection problem is formulated as a many-objective problem. Nondominated Sorting based Genetic Algorithm (NSGA-III), and Multi-Objective Evolutionary Algorithm based on Decomposition (MOEA/D), which are Many-Objective evolutionary algorithms, have been applied and investigated for optimal tag SNPs selection. This study also investigates different initialization methods like greedy and random initialization. optimization.ResultsThe evaluation measures used for comparing results for different algorithms are Hypervolume, Range, SumMin, MinSum, Tolerance rate, and Average Hamming distance. Overall MOEA/D algorithm gives superior results as compared to other algorithms in most cases. NSGA-III outperforms NSGA-II and other compared algorithms on maximum tolerance rate, and SPEA2 outperforms all algorithms on average hamming distance.ConclusionExperimental results show that the performance of our proposed many-objective algorithms is much superior as compared to the results of existing methods. The outcomes show the advantages of greedy initialization over random initialization using NSGA-III, SPEA2, and MOEA/D to solve the tag SNPs selection as many-objective optimization problem.

Dataset Information

Evaluating and Improving Automatic Sleep Spindle Detection by Using Multi-Objective Evolutionary Algorithms.

Publications

Evaluating and Improving Automatic Sleep Spindle Detection by Using Multi-Objective Evolutionary Algorithms.

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