Doktora Tezleri
Permanent URI for this collectionhttps://hdl.handle.net/20.500.12573/5800
Browse
3 results
Search Results
Doctoral Thesis Biyoçipler için Mikro Biyomalzemelerin ve Hücrelerin Görüntü İşleme Yöntemleri ile Otomatik Olarak Sayılması ve Analizi(Abdullah Gül Üniversitesi, Fen Bilimleri Enstitüsü, 2023) Çelebi, Fatma; İçöz, KutayQuantification of tumor cells is essential for early cancer detection and progression tracking. Multiple techniques have been devised to detect tumor cells. In addition to conventional laboratory instruments, several biochip-based techniques have been devised for this purpose. Our biochip design incorporates micron-sized immunomagnetic beads and micropad arrays, necessitating automated detection and quantification not only of cells but also of the micropads and immunomagnetic beads. The primary function of the biochip is to simultaneously acquire target cells with distinct antigens. As a readout technique for the biochip, this study devised a digital image processing-based method for quantifying leukemia cells, immunomagnetic beads, and micropads. Images were acquired on the chip using bright-field microscopy with image objectives of 20X and 40X. Conventional image processing methods, machine learning methods, and deep learning methods were used to analyze the images. To quantify targets in the images captured by a bright-field microscope, color- and size-based object recognition and machine learning-based methods were first implemented. Secondly, color- and size-based object detection and object segmentation methods were implemented to detect structures in bright-field optical microscope images acquired from the biochip. Third, segmentation of the minimal residual disease (MRD) using deep learning. Implemented biochip images comprised of leukemic cells, immunomagnetic beads, and micropads. Moreover, mesenchymal stem cells (MSCs) are stem cells with the capacity for multilineage differentiation and self-renewal. Estimating the proportion of senescent cells is therefore essential for clinical applications of MSCs. In this study, a self-supervised learning (SSL)-based method for segmenting and quantifying the density of cellular senescence was implemented, which can perform well despite the small size of the labeled dataset.Doctoral Thesis Makine Öğrenmesi Yöntemleriyle Antimikrobiyal Peptit Aktivite Tahmini(Abdullah Gül Üniversitesi, Fen Bilimleri Enstitüsü, 2023) Söylemez, Ümmü Gülsüm; Güngör, BurcuAntimicrobial peptides (AMPs) are considered as promising alternatives to conventional antibiotics in order to overcome the growing problems of antibiotic resistance. Computational prediction approaches receive an increasing interest to identify and design the best candidate AMPs prior to the in vitro tests. In this thesis, using the multiple properties of the peptides we aimed to develop machine learning approaches that can predict the antimicrobial activities of the peptides. We have created two datasets for the peptides showing antimicrobial activity against Gram-negative and against Gram-positive bacteria separately. In our first study, ten different physico-chemical properties of the peptides were calculated, and used as features of the peptides. Following the data exploration and data preprocessing steps, a variety of classification models were build with 100-fold Monte Carlo Cross-Validation; and the performance of these models were evaluated. In the second study, we proposed a novel method called AMP-GSM. The method was tested for three datasets, and the prediction performance of AMP-GSM was comparatively evaluated with several feature selection methods and several classifiers. In the last study, using motif matching score with the models of activity against Gram-positive and Gram-negative bacteria, we created novel peptides and predicted the target selectivity of these peptides. The studies presented in this thesis advance the field of computational research by making it easier to predict the possible antimicrobial effects of peptides and to design AMPs in wet laboratory environments.Doctoral Thesis Protein Yapı Tahmini için Derin Öğrenme Modellerinin Geliştirilmesi(Abdullah Gül Üniversitesi, Fen Bilimleri Enstitüsü, 2022) Görmez, Yasin; Aydın, ZaferThe three-dimensional structure of a protein provides important clues about the function of that protein. Although there have been many studies on protein structure prediction, the problem has still not been solved completely. As it is very difficult to predict the three-dimensional structure of a protein directly, predictions of structural properties of proteins such as secondary structure, solvent accessibility, and torsion angles are carried out first, which are later used as inputs to more elaborate structure estimation tasks. In this thesis, novel deep learning models have been developed by using convolutional neural networks (CNN), graph convolutional networks (GCN) and long-short-term memory (LSTM) recurrent neural networks to predict secondary structure, solvent accessibility and torsion angles of proteins. A rich feature set formed by using PSI-BLAST, HHBlits, physicochemical properties, structural profile matrices, AA index values, and graphs representing the relationship between amino acids were used as inputs to the models. In the first study, a deep learning model was developed by using CNN and GCN layers for secondary structure prediction. In the second study, LSTM layers were added to the first model, which was extended to make solvent accessibility and torsion angle predictions as well using the multi-task learning approach. In both studies, graphs were generated using neighborhood relations between amino acids. In the last study, a novel U-net-based model was designed for secondary structure prediction using CNN, GCN, and LSTM layers. The graph matrices used as input to GCN layers were obtained by using protein contact map prediction. All models were trained, optimized and tested on benchmark data sets. Improvements were obtained in accuracy as compared to the state-of-the-art