Searching for new genes associated with the familial hypercholesterolemia phenotype using whole-genome sequencing and machine learning

Searching for new genes associated with the familial hypercholesterolemia phenotype using whole-genome sequencing and machine learning

One of the most common congenital metabolic disorders is familial hypercholesterolemia. Familial hyper-cholesterolemia is a condition caused by a type of genetic defect leading to a decreased rate of removal of low-density lipoproteins from the bloodstream and a pronounced increase in the blood leve...

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Bibliographic Details
Main Authors: D. E. Ivanoshchuk, A. B. Kolker, O. V. Timoshchenko, S. E. Semaev, E. V. Shakhtshneider
Format: Article
Language:English
Published: Siberian Branch of the Russian Academy of Sciences, Federal Research Center Institute of Cytology and Genetics, The Vavilov Society of Geneticists and Breeders 2023-09-01
Series:Вавиловский журнал генетики и селекции
Subjects:
familial hypercholesterolemia
whole-genome sequencing
machine learning
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Online Access:https://vavilov.elpub.ru/jour/article/view/3868
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