Show/Hide Menu
Hide/Show Apps
Logout
Türkçe
Türkçe
Search
Search
Login
Login
OpenMETU
OpenMETU
About
About
Open Science Policy
Open Science Policy
Open Access Guideline
Open Access Guideline
Postgraduate Thesis Guideline
Postgraduate Thesis Guideline
Communities & Collections
Communities & Collections
Help
Help
Frequently Asked Questions
Frequently Asked Questions
Guides
Guides
Thesis submission
Thesis submission
MS without thesis term project submission
MS without thesis term project submission
Publication submission with DOI
Publication submission with DOI
Publication submission
Publication submission
Supporting Information
Supporting Information
General Information
General Information
Copyright, Embargo and License
Copyright, Embargo and License
Contact us
Contact us
COMPARATIVE ANALYSIS OF BRAIN CELL CULTURES AND TISSUES IN ALZHEIMER’S DISEASE BASED ON DIFFERENTIAL EXPRESSION AND GENE SET ENRICHMENT
Download
10525198.pdf
Date
2023-1-25
Author
Burduroğlu, Hüseyin Cahit
Metadata
Show full item record
This work is licensed under a
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
.
Item Usage Stats
301
views
355
downloads
Cite This
Alzheimer’s disease is currently the most common cause of dementia in the world. It is a neurodegenerative disease that is diagnosed neuropathologically by observing B-amyloid plaques and neurofibrillary tangles in the brain. Transcriptional differentiations, protein regulations, and the interactions in between have been investigated by recent studies to understand from which brain cell type the disease stems, such as microglia, astrocytes, and neurons. These studies are mostly performed on brain tissue samples that bring certain challenges. With the addition of novel gene editing methods in recent years, cell models are gaining popularity as an alternative to studying Alzheimer’s disease. Yet, due to the complicated nature of the disease, cell models may not be representative enough. This study aims to determine the representativeness of cell models, in contrast to brain tissue samples, by comparing the two groups by their differentially expressed genes and enriched cellular functions. For this purpose, 19 projects (10 tissues, 9 cells) were selected for analysis from NCBI BioProject, which were then grouped by sex and cell types. The comparisons were made using the number of genes in gene sets that enrich certain biological processes. Distance matrices and topology plots were used for visualization.
Subject Keywords
Alzheimer's
,
transcriptomics
,
meta-analysis
,
differential expression
,
gene set enrichment
,
cell models
URI
https://hdl.handle.net/11511/102037
Collections
Graduate School of Informatics, Thesis
Suggestions
OpenMETU
Core
COMPARISON OF ENTROPY AND ENSEMBLE-BASED FEATURE SELECTION THROUGH NETWORK ANALYSIS OF ALZHEIMERS DISEASE-ASSOCIATED VARIANTS
Rafatov, Sevda; Aydın Son, Yeşim; Department of Bioinformatics (2022-2-7)
Alzheimer’s Disease (AD) is a complex, progressive and irreversible brain disorder that slowly destroys memory and thinking skills and eventually loses the ability to do daily tasks. Our group is currently developing in-silico AD models in which genotyping and phenotyping data are integrated for the differential diagnosis Late-On-Set AD (LOAD) cases. Meta-analysis of four different LOAD data sets provided by ADNI and dbGAP, which includes the genotyping data of more than 5000 LOAD patients, is done. In this...
Fluorescent labeling of SPOCK1 and localization studies in live neural cell lines
Karaboğa, Zeynep Eda; Son, Çağdaş Devrim; Aydın Son, Yeşim; Department of Biology (2022-11-30)
Alzheimer's disease is the most common form of dementia and is incurable. The late onset Alzheimer’s disease (LOAD) is associated with complex genetic transition, and the molecular background has not been enlightened yet. Our previous research on the meta-analysis of genome-wide association studies (GWAS) showed a statistical correlation between SPOCK1 variants and LOAD. Also, it is co-regulated with apolipoprotein (APP), one of the proteins clinically linked with LOAD. Furthermore, the SPOCK1 protein ...
Investigating conversion from mild cognitive impairment to alzheimer's disease using latent space manipulation
Ayvaz, Deniz Sezin; Baytaş, İnci M. (Orta Doğu Teknik Üniversitesi Enformatik Enstitüsü; 2022-10)
Alzheimer’s disease, a progressive neurologic disorder, is the most common cause of dementia, affecting millions worldwide. Mild Cognitive Impairment (MCI) is considered an intermediate stage before Alzheimer's. Early prediction of the conversion from MCI to Alzheimer's is crucial to take necessary precautions for decelerating the disease progression and developing suitable treatments. This study proposes a deep learning framework to identify patients whose diagnoses might change from MCI to Alzheimer’s in ...
Gene-level pathogenicity scores for alzheimer’s disease using genomic variants from rna-seq data
Bozkurt, Fatma Betül; İlgün, Atılay; Uzuner, Dilara; Çakır, Tunahan (Orta Doğu Teknik Üniversitesi Enformatik Enstitüsü; 2022-10)
Alzheimer’s disease (AD) is a complex neurodegenerative disorder affecting millions of people worldwide. Next-generation sequencing technologies such as whole-exome/genome sequencing have been widely used for detecting the variants in the genome to understand the disease etiology and unravel underlying molecular mechanisms. Alternatively, RNA-Seq data can also be used to detect variants. Since AD is a complex disease, several variants are involved in the disease pathogenesis. By using scoring algorithms, it...
A human carboxypeptidase E/NF-alpha 1 gene mutation in an Alzheimer's disease patient leads to dementia and depression in mice
Cheng, Y.; Cawley, N. X.; Yanık, Tülin; Murthy, S. R. K.; Liu, C.; Kasikci, F.; Abebe, D.; Loh, Y. P. (2016-12-06)
Patients with Alzheimer's disease (AD), a common dementia among the aging population, often also suffer from depression. This comorbidity is poorly understood. Although most forms of AD are not genetically inherited, we have identified a new human mutation in the carboxypeptidase E (CPE)/neurotrophic factor-alpha 1 (NF-alpha 1) gene from an AD patient that caused memory deficit and depressive-like behavior in transgenic mice. This mutation consists of three adenosine inserts, introducing nine amino acids, i...
Citation Formats
IEEE
ACM
APA
CHICAGO
MLA
BibTeX
H. C. Burduroğlu, “COMPARATIVE ANALYSIS OF BRAIN CELL CULTURES AND TISSUES IN ALZHEIMER’S DISEASE BASED ON DIFFERENTIAL EXPRESSION AND GENE SET ENRICHMENT,” M.S. - Master of Science, Middle East Technical University, 2023.