Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
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Article Citation - WoS: 6Citation - Scopus: 7Time-Resolved Eeg Signal Analysis for Motor Imagery Activity Recognition(Elsevier, 2023) Olcay, Bilal Orkan; Karaçalı, BilgeAccurately characterizing brain activity requires detailed feature analysis in the temporal, spatial, and spectral domains. While previous research has proposed various spatial and spectral feature extraction methods to distinguish between different cognitive tasks, temporal feature analysis for each separate brain region and frequency band has been largely overlooked. This study introduces two novel approaches for recognizing cognitive activity: temporal entropic profiling and time-aligned common spatio-spectral patterns analysis. These approaches capture and use discriminative short-lived signal segments for motor imagery activity recognition. In Approach-1, we evaluated nine different measures to determine timing parameters that showed altered behavior associated with maximal inter-activity differences, which we then used in a machine-learning framework. In Approach-2, we used the best-performing signal characteristic measures from Approach-1 to determine the optimum latency of each channel at each frequency band for a CSP-based activity recognition strategy. We evaluated both approaches on two online available motor imagery EEG datasets and achieved average recognition accuracy levels of 86%. We compared our methods with four established BCI methods. The performance results show that our approaches exceeded the benchmark methods' performances, with notable improvements in the proposed time-aligned common spatio-spectral patterns approach. This study demonstrates that motor imagery recognition performance is improved when a temporal analysis is adopted alongside spatio-spectral neural feature analysis and that timing parameters associated with the maximal entropic difference of EEG segments to the cognitive tasks varied between different brain regions and subjects. © 2023 Elsevier LtdArticle Citation - WoS: 3Citation - Scopus: 4Quasi-Supervised Strategies for Compound-Protein Interaction Prediction [article](Wiley-VCH Verlag, 2021) Çakı, Onur; Karaçalı, BilgeIn-silico compound-protein interaction prediction addresses prioritization of drug candidates for experimental biochemical validation because the wet-lab experiments are time-consuming, laborious and costly. Most machine learning methods proposed to that end approach this problem with supervised learning strategies in which known interactions are labeled as positive and the rest are labeled as negative. However, treating all unknown interactions as negative instances may lead to inaccuracies in real practice since some of the unknown interactions are bound to be positive interactions waiting to be identified as such. In this study, we propose to address this problem using the Quasi-Supervised Learning (QSL) algorithm. In this framework, potential interactions are predicted by estimating the overlap between a true positive dataset of compound-protein pairs with known interactions and an unknown dataset of all the remaining compound-protein pairs. The potential interactions are then identified as those in the unknown dataset that overlap with the interacting pairs in the true positive dataset in terms of the associated similarity structure. We also address the class-imbalance problem by modifying the conventional cost function of the QSL algorithm. Experimental results on GPCR and Nuclear Receptor datasets show that the proposed method can identify actual interactions from all possible combinations.Article Citation - WoS: 10Citation - Scopus: 13On the Characterization of Cognitive Tasks Using Activity-Specific Short-Lived Synchronization Between Electroencephalography Channels(Elsevier, 2021) Olcay, B. Orkan; Özgören, Murat; Karaçalı, BilgeAccurate characterization of brain activity during a cognitive task is challenging due to the dynamically changing and the complex nature of the brain. The majority of the proposed approaches assume stationarity in brain activity and disregard the systematic timing organization among brain regions during cognitive tasks. In this study, we propose a novel cognitive activity recognition method that captures the activity-specific timing parameters from training data that elicits maximal average short-lived pairwise synchronization between electroencephalography signals. We evaluated the characterization power of the activity-specific timing parameter triplets in a motor imagery activity recognition framework. The activity-specific timing parameter triplets consist of latency of the maximally synchronized signal segments from activity onset Delta t, the time lag between maximally synchronized signal segments t, and the duration of the maximally synchronized signal segments w. We used cosine-based similarity, wavelet bi-coherence, phase-locking value, phase coherence value, linearized mutual information, and cross-correntropy to calculate the channel synchronizations at the specific timing parameters. Recognition performances as well as statistical analyses on both BCI Competition-III dataset IVa and PhysioNet Motor Movement/Imagery dataset, indicate that the interchannel short-lived synchronization calculated using activity-specific timing parameter triplets elicit significantly distinct synchronization profiles for different motor imagery tasks and can thus reliably be used for cognitive task recognition purposes. (C) 2021 Elsevier Ltd. All rights reserved.Article Citation - WoS: 3Citation - Scopus: 3Automated Labeling of Cancer Textures in Larynx Histopathology Slides Using Quasi-Supervised Learning(Science Printers and Publishers Inc., 2014) Önder, Devrim; Sarıoğlu, Sülen; Karaçalı, BilgeOBJECTIVE: To evaluate the performance of a quasisupervised statistical learning algorithm, operating on datasets having normal and neoplastic tissues, to identify larynx squamous cell carcinomas. Furthermore, cancer texture separability measures against normal tissues are to be developed and compared either for colorectal or larynx tissues. STUDY DESIGN: Light microscopic digital images from histopathological sections were obtained from laryngectomy materials including squamous cell carcinoma and nonneoplastic regions. The texture features were calculated by using co-occurrence matrices and local histograms. The texture features were input to the quasisupervised learning algorithm. RESULTS: Larynx regions containing squamous cell carcinomas were accurately identified, having false and true positive rates up to 21% and 87%, respectively. CONCLUSION: Larynx squamous cell carcinoma versus normal tissue texture separability measures were higher than colorectal adenocarcinoma versus normal textures for the colorectal database. Furthermore, the resultant labeling performances for all larynx datasets are higher than or equal to that of colorectal datasets. The results in larynx datasets, in comparison with the former colorectal study, suggested that quasi-supervised texture classification is to be a helpful method in histopathological image classification and analysis.Article Identification and Visualization of Cell Subgroups in Uncompensated Flow Cytometry Data(Elsevier Ltd., 2020) Güzel, Başak Esin Köktürk; Karaçalı, BilgeWe propose a new method for identification and visualization of cell-sub groups in uncompensated multi-color flow cytometry data. The method combines annealing-based model-free expectation-maximization to identify cell sub-groups and joint diagonalization on clustered data for better visualization. The proposed method was evaluated on a real, publicly available 8-color flow cytometry dataset manually gated beforehand for lymphocytes. The results obtained in three separable scenarios indicate that the method accurately identifies cell subgroups while properly adjusting visualization of identified cell groups by reducing the spectral overlap between the different fluorochrome channels.Conference Object Citation - Scopus: 2Model-Free Expectation Maximization for Divisive Hierarchical Clustering of Multicolor Flow Cytometry Data(IEEE, 2014) Köktürk, Başak Esin; Karaçalı, BilgeThis paper proposes a new method for automated clustering of high dimensional datasets. The method is based on a recursive binary division strategy that successively divides an original dataset into distinct clusters. Each binary division is carried out using a model-free expectation maximization scheme that exploits the posterior probability computation capability of the quasi-supervised learning algorithm. The divisions are carried out until a division cost exceeds an adaptively determined limit. Experiment results on synthetic as well as real multi-color flow cytometry datasets showed that the proposed method can accurately capture the prominent clusters without requiring any knowledge on the number of clusters or their distribution models.Conference Object Citation - Scopus: 1Hierarchical Motif Vectors for Amino Acid Sequence Alignment(2012) Karaçalı, BilgeWe present a new framework for global and local alignment of amino acid sequences based on hierarchical motif vectors that characterize local amino acid configurations. The motif vectors are constructed by carrying out wavelet decomposition on numeric property sequences obtained by replacing each amino acid in a sequence with their respective properties, and concatenating such profiles obtained for a large number of physico-chemical properties into a single column vector. We then formulate different schemes for aligning amino acid sequences based on their respective motif vectors globally as well as locally subject to measures of statistical significance. Experiment results indicate that the motif vectors accurately capture the amino acid composition at and around individual sites along sequences and allow associating sequence segments sharing similar functional attributes.Article Citation - WoS: 14Citation - Scopus: 17Evaluation of Synchronization Measures for Capturing the Lagged Synchronization Between Eeg Channels: a Cognitive Task Recognition Approach(Elsevier, 2019) Olcay, Bilal Orkan; Karaçalı, BilgeDuring cognitive, perceptual and sensory tasks, connectivity profile changes across different regions of the brain. Variations of such connectivity patterns between different cognitive tasks can be evaluated using pairwise synchronization measures applied to electrophysiological signals, such as electroencephalography (EEG). However, connectivity-based task recognition approaches achieving viable recognition performance have been lacking from the literature. By using several synchronization measures, we identify time lags between channel pairs during different cognitive tasks. We employed mutual information, cross correntropy, cross correlation, phase locking value, cosine similarity and nonlinear interdependence measures. In the training phase, for each type of cognitive task, we identify the time lags that maximize the average synchronization between channel pairs. These lags are used to calculate pairwise synchronization values with which we construct the train and test feature vectors for recognition of the cognitive task carried out using Fisher's linear discriminant (FLD) analysis. We tested our framework in a motor imagery activity recognition scenario on PhysioNet Motor Movement/Imagery and BCI Competition-III IVa datasets. For PhysioNet dataset, average performance results ranging between % 51 and % 61 across 20 subjects. For BCI Competition-III dataset, we achieve an average recognition performance of % 76 which is above the minimum reliable communication rate (% 70). We achieved an average accuracy over the minimum reliable communication rate on the BCI Competition-III dataset. Performance levels were lower on the PhysioNet dataset. These results indicate that a viable task recognition system is achievable using pairwise synchronization measures evaluated at the proper task specific lags.Conference Object 2-D Thresholding of the Connectivity Map Following the Multiple Sequence Alignments of Diverse Datasets(ACTA Press, 2013) Doğan, Tunca; Karaçalı, BilgeMultiple sequence alignment (MSA) is a widely used method to uncover the relationships between the biomolecular sequences. One essential prerequisite to apply this procedure is to have a considerable amount of similarity between the test sequences. It's usually not possible to obtain reliable results from the multiple alignments of large and diverse datasets. Here we propose a method to obtain sequence clusters of significant intragroup similarities and make sense out of the multiple alignments containing remote sequences. This is achieved by thresholding the pairwise connectivity map over 2 parameters. The first one is the inferred pairwise evolutionary distances and the second parameter is the number of gapless positions on the pairwise comparisons of the alignment. Threshold curves are generated regarding the statistical parameter values obtained from a shuffled dataset and probability distribution techniques are employed to select an optimum threshold curve that eliminate as much of the unreliable connectivities while keeping the reliable ones. We applied the method on a large and diverse dataset composed of nearly 18000 human proteins and measured the biological relevance of the recovered connectivities. Our precision measure (0.981) was nearly 20% higher than the one for the connectivities left after a classical thresholding procedure displaying a significant improvement. Finally we employed the method for the functional clustering of protein sequences in a gold standard dataset. We have also measured the performance, obtaining a higher F-measure (0.882) compared to a conventional clustering operation (0.827).Article Citation - WoS: 560Citation - Scopus: 607A Community Effort To Assess and Improve Drug Sensitivity Prediction Algorithms(Nature Publishing Group, 2014) Costello, James C.; Heiser, Laura M.; Georgii, Elisabeth; Gönen, Mehmet; Menden, Michael P.; Wang, Nicholas J.; Bansal, Mukesh; Ammad-ud-din, Muhammad; Hintsanen, Petteri; Khan, Suleiman A.; Mpindi, John-Patrick; Kallioniemi, Olli; Honkela, Antti; Aittokallio, Tero; Wennerberg, Krister; NCI-DREAM Community; Karaçalı, Bilge; Collins, James J.; Gallahan, Dan; Singer, Dinah; Saez-Rodriguez, Julio; Kaski, Samuel; Gray, Joe W.; Stolovitzky, GustavoPredicting the best treatment strategy from genomic information is a core goal of precision medicine. Here we focus on predicting drug response based on a cohort of genomic, epigenomic and proteomic profiling data sets measured in human breast cancer cell lines. Through a collaborative effort between the National Cancer Institute (NCI) and the Dialogue on Reverse Engineering Assessment and Methods (DREAM) project, we analyzed a total of 44 drug sensitivity prediction algorithms. The top-performing approaches modeled nonlinear relationships and incorporated biological pathway information. We found that gene expression microarrays consistently provided the best predictive power of the individual profiling data sets; however, performance was increased by including multiple, independent data sets. We discuss the innovations underlying the top-performing methodology, Bayesian multitask MKL, and we provide detailed descriptions of all methods. This study establishes benchmarks for drug sensitivity prediction and identifies approaches that can be leveraged for the development of new methods.
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