Scopus İndeksli Yayınlar Koleksiyonu

Permanent URI for this collectionhttps://hdl.handle.net/20.500.12573/395

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Now showing 1 - 7 of 7
  • Conference Object
    Identify Commonly Affected Pathways in Psychiatric Diseases
    (Institute of Electrical and Electronics Engineers Inc., 2018-09) Bulut, Umit; Bakir-Güngör, Burcu
    Genome-wide association studies (GWAS) are an extraordinary source of information when it comes to revealing the common variations of human complex diseases. Until now, the large amount of data generated from these studies have not been shown its full potential enough to identify the molecular and functional framework to be able to understand how a molecular system works. Following a more specific perspective, this study focused on the identification of commonly affected pathways of psychiatric diseases. The pathway term as used in molecular biology, depicts a simplified model of a process within the cell or tissue. Lately, several GWAS datasets are publicly available for various disease types such as psychiatric, immune-related, neurodegenerative, cardiovascular and such. A study on each disease and pairwise comparison to understand the behavior of disease and system would be time consuming and exhaustive. Instead of handling the results of these studies one by one, grouping diseases by target points is a more efficient way. This work aims to get one step closer to reveal key points of diseases and target these points to develop personalized medicine approaches. Especially for complex diseases, every drug doesn't show the same effect in every people. This paper contains the definition of molecular pathways, methods to identify disease related pathways, and to find common pathways pairwise in psychiatric diseases. © 2019 Elsevier B.V., All rights reserved.
  • Conference Object
    Citation - Scopus: 8
    Constructing Structural Profiles for Protein Torsion Angle Prediction
    (SciTePress, 2015) Aydin, Zafer; Baker, David A.; Noble, William Stafford
    Structural frequency profiles provide important constraints on structural aspects of a protein and is receiving a growing interest in the structure prediction community. In this paper, we introduce new techniques for scoring templates that are later combined to form structural profiles of 7-state torsion angles. By employing various parameters of target-template alignments we improve the quality and accuracy of structural profiles considerably. The most effective technique is the scaling of templates by integer powers of sequence identity score in which the power parameter is adjusted with respect to the similarity interval of the target. Incorporating other alignment scores as multiplicative factors further improves the accuracy of profiles. After analyzing the individual strengths of various structural profile methods, we combine them with ab-initio predictions of 7-state torsion angles by a linear committee approach. We show that incorporating template information improves the accuracy of ab-initio predictions significantly at all levels of target-template similarity even when templates are distant from the target. Template scaling methods developed in this work can be applied in many other prediction tasks and in more advanced methods designed for computing structural profiles. © 2020 Elsevier B.V., All rights reserved.
  • Conference Object
    Citation - WoS: 3
    Citation - Scopus: 2
    Combining Classifiers for Protein Secondary Structure Prediction
    (IEEE, 2017) Aydin, Zafer; Uzut, Ommu Gulsum
    Protein secondary structure prediction is an important step in estimating the three dimensional structure of proteins. Among the many methods developed for predicting structural properties of proteins, hybrid classifiers and ensembles that combine predictions from several models are shown to improve the accuracy rates. In this paper, we train, optimize and combine a support vector machine, a deep convolutional neural field and a random forest in the second stage of a hybrid classifier for protein secondary structure prediction. We demonstrate that the overall accuracy of the proposed ensemble is comparable to the success rates of the state-of-the-art methods in the most difficult prediction setting and combining the selected models have the potential to further improve the accuracy of the base learners.
  • Conference Object
    Citation - WoS: 2
    Citation - Scopus: 2
    Classification of Breast Cancer Molecular Subtypes With Grouping-Scoring Approach That Incorporates Disease-Disease Association Information
    (IEEE, 2024-05-15) Qumsiyeh, Emma; Bakir-Gungor, Burcu; Yousef, Malik
    This study uses modern sequencing technology and large biological databases to investigate the molecular intricacies of complicated diseases like cancer. Using gene expression databases and biomarkers, the research aims to improve breast cancer molecular subtype identification for better patient outcomes. Using BRCA LumAB_ Her2Basal dataset, this study compares an integrative machine learning-based strategy (GediNET) to traditional feature selection approaches across machine learning classifiers. GediNET excels at uncovering crucial disease-disease connections and potential biomarkers using the Grouping-Scoring-Modeling (GSM) approach, which favors gene groupings above individual genes. Our comparative analysis highlights GediNET's exceptional performance, notably in terms of accuracy and Area Under the Curve metrics, underscoring its effectiveness in uncovering the genetic intricacies of breast cancer. GediNET's promise to improve disease classification and biomarker identification by improving biological mechanism understanding goes beyond exceeding traditional approaches. The work shows that GediNET's integrative method can promote bioinformatics research by identifying the most informative genes associated with certain diseases, enabling focused and customized medicine.
  • Conference Object
    Citation - Scopus: 3
    A Computational Drug Repositioning Effort Using Patients' Reviews Dataset
    (Institute of Electrical and Electronics Engineers Inc., 2023-07-25) Akkaya, Ali; Bakal, Gokhan
    The drug discovery process is one of the core motivations in both medical and, specifically, pharmaceutical disciplines. Due to the nature of the process, it requires an excessive amount of time, clinical experiments, and budget to cover each discovery phase. In this sense, computational drug discovery efforts can shorten the discovery process by providing plausible candidates since many of the attempts fail for several reasons, such as a lack of participants, financial problems, or ineffective results. In this study, the goal is to identify plausible candidate drugs for diseases. To do that, we utilize a personal experience of drugs dataset generated by patients. Beyond the user-generated comments, the users also give a rate between 1 and 10. Since we want to ensure the dataset quality, we first performed sentiment analysis experiments to prove that the reviews/comments are consistent with the given rating score. Then, only the review pairs having an effectiveness rate of 6 or more are selected as pre-filtered drug-disease pairs. We also build a knowledge graph using treatment-related biomedical relations using predications from Semantic Medline Database to identify drug similarities utilizing the Simrank similarity algorithm. As a result, we reported a list of plausible drugs as repurposing/repositioning candidates for further experiments. © 2023 Elsevier B.V., All rights reserved.
  • Conference Object
    A Comparative Study on Psychiatric Disorders: Identification of Shared Pathways and Common Agents
    (Institute of Electrical and Electronics Engineers Inc., 2022-09-07) Kuzudisli, Cihan; Bakir-Güngör, Burcu; Bakir Gungor, Burcu
    Distinct but closely related diseases generally present shared symptoms, which address possible overlaps among their pathogenic mechanisms. Identification of significantly impacted shared pathways and other common agents are expected to elucidate etiology of these disorders and to help design better intervention strategies. In this research effort, we studied six psychiatric disorders including schizophrenia (SCZ), anorexia (AN), bipolar disorder (BD), depressive disorder (DD), autism (AU) and attention deficit hyperactivity disorder (ADHD). Our methodology can be classified into the following two parts: In Part I, common susceptibility genes; and in Part II, genome-wide association studies (GWAS) data were used to find enriched pathways of psychiatric disorders. 59 KEGG pathways were commonly identified in both parts. 31 of these pathways are disease pathways. Pathways related to cancer and infectious diseases were predominant compared to others. Most of the acquired pathways were in accordance with previous studies in literature. A combination of susceptibility genes and GWAS data is an effective approach to identify significantly impacted pathways in multifactorial diseases. In this respect, shared modules were determined after applying hierarchical clustering of the enriched pathways. These identified modules may tell us the association of psychiatric disorders with the enriched pathways. Taken all together, common pathways and shared modules are expected to highlight the causative factors and important mechanisms behind complex psychiatric diseases, leading to effective drug discovery. © 2022 Elsevier B.V., All rights reserved.
  • Conference Object
    Citation - Scopus: 13
    Staging of the Liver Fibrosis From CT Images Using Texture Features
    (2012) Kayaaltı, Ömer; Aksebzeci, Bekir Hakan; Karahan, Ökkeş Ibrahim; Deniz, Kemal; Öztürk, Menmet; Yilmaz, Bulent; Asyali, Musa Hakan; Karahan, Ibrahim Ö.
    Even though liver biopsy is critical for evaluating chronic hepatitis and fibrosis, it is an invasive, costly, and difficult to standardize approach. The developments in medical image processing and artificial intelligence methods have advanced the potential of using computer-aided diagnosis techniques in the classification of liver tissues. The aim of this study was to develop a non-invasive, cost-effective, and fast approach to specify fibrosis stage using the texture properties of computed tomography images of liver. Gray level co-occurrence matrix, discrete wavelet transform, and discrete Fourier transform were the image analysis tools in the feature extraction phase. Following dimension reduction of the texture features support vector machines and k-nearest neighbor methods were used in the classification phase of this study. Our results showed that our approach is feasible in fibrosis staging especially in pairwise stage comparisons with success rate of approximately 90%. © 2012 IEEE. © 2012 Elsevier B.V., All rights reserved.