Abstract
The possibility of quick decoding of individual human genome has allowed us to amass vast data arrays of diseases, as well as associated human DNA mutations. It is well-known that DNA mutations cause genetic diseases and disorders. Among the risk group of severe coronavirus disease cases are patients with preexisting cardiovascular or respiratory diseases, oncologic pathologies, hypertension, and other disorders. Coronavirus disease severity can be predicted using machine learning methods trained on features corresponding to single nucleotide polymorphisms in gene coding sequences of patient genomes.
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Biletskyy, B., Gupal, A. (2021). Risk Group Determination in Case of COVID-19 Infection. In: Rojas, I., Castillo-Secilla, D., Herrera, L.J., Pomares, H. (eds) Bioengineering and Biomedical Signal and Image Processing. BIOMESIP 2021. Lecture Notes in Computer Science(), vol 12940. Springer, Cham. https://doi.org/10.1007/978-3-030-88163-4_36
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DOI: https://doi.org/10.1007/978-3-030-88163-4_36
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