English logo
Boğaziçi University Library
Digital Archive
  • English
  • Català
  • Čeština
  • Deutsch
  • Español
  • Français
  • Gàidhlig
  • Italiano
  • Latviešu
  • Magyar
  • Nederlands
  • Polski
  • Português
  • Português do Brasil
  • Srpski (lat)
  • Suomi
  • Svenska
  • Türkçe
  • Tiếng Việt
  • Қазақ
  • বাংলা
  • हिंदी
  • Ελληνικά
  • Српски
  • Yкраї́нська
  • Log In
    New user? Click here to register. Have you forgotten your password?
English logo
Boğaziçi University Library
Digital Archive
  • Communities & Collections
  • All of DSpace
  • English
  • Català
  • Čeština
  • Deutsch
  • Español
  • Français
  • Gàidhlig
  • Italiano
  • Latviešu
  • Magyar
  • Nederlands
  • Polski
  • Português
  • Português do Brasil
  • Srpski (lat)
  • Suomi
  • Svenska
  • Türkçe
  • Tiếng Việt
  • Қазақ
  • বাংলা
  • हिंदी
  • Ελληνικά
  • Српски
  • Yкраї́нська
  • Log In
    New user? Click here to register. Have you forgotten your password?
  1. Home
  2. Browse by Author

Browsing by Author "Kartal, Ece."

Now showing 1 - 1 of 1
Results Per Page
Sort Options
  • Loading...
    Thumbnail Image
    Item
    Identification of pathogenic mutations in neurodegenerative disorders: bioinformatic analysis of next generation sequencing data
    (Thesis (M.S.) - Bogazici University. Institute for Graduate Studies in Science and Engineering, 2015., 2015.) Kartal, Ece.; Başak, A. Nazlı.
    Neurodegenerative diseases, such as Alzheimer’s disease, Parkinson’s disease, amyotrophic lateral sclerosis and ataxias belong to a large group of disorders, characterized by progressive neuronal cell death in specific parts of the brain. They exhibit Mendelian and also complex inheritance patterns, thus a deeper understanding of genetic factors underlying disease pathogenesis is crucial to improve new and more targeted therapy methods. Next generation sequencing is a highly efficient and powerful method for the identification of disease-causing variants in complex disorders. In the framework of this study, one dominant and 12 recessive pedigrees were subjected to exome sequencing. Selection of families was performed by considering factors, such as consanguinity and the presence of more than one affected member in the family. Homozygosity mapping was performed for determination of homozygous stretches. Candidate variants were validated in family members and segregation of mutations in the families was shown. The data and bioinformatic analyses methods described above were for the first time adapted, developed and applied to several families in our laboratory within this thesis work. The analysis of next generation sequencing data is expected to unravel the genetic factors that cause neurodegeneration in these complex syndromes.

DSpace software copyright © 2002-2025 LYRASIS

  • Cookie settings
  • Send Feedback