Zobrazeno 1 - 2
of 2
pro vyhledávání: '"N. D.K. Ranadeva"'
Autor:
P. J. Wijekumar, N. D.K. Ranadeva, A. R. Jayamaha, H. M.N.D.M. Herath, N. Noorden, S. S.N. Fernando
Publikováno v:
BMC Research Notes, Vol 16, Iss 1, Pp 1-6 (2023)
Abstract Objectives A SNV is a single nucleotide change that can occur at any point in the genome. SNVs are the most common genetic variants that occur in the human genome, and a number of SNVs have been found to be associated with human traits and d
Externí odkaz:
https://doaj.org/article/8ca79d466f254f8cb71a594a002e6e5a
Autor:
P. J. Wijekumar, N. D.K. Ranadeva, A. R. Jayamaha, H.M.N.D.M Herath, N. Noorden, S.S.N. Fernando
Objectives: SNV is a single nucleotide change that can occur at any point in the genome. It is regarded as a frequent genetic variant that can result in genetic diseases. Discovering genetic variants in individuals is one of the most essential jobs o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1b4e75a99f4b20afea6b69dd93996ff
https://doi.org/10.21203/rs.3.rs-2507288/v1
https://doi.org/10.21203/rs.3.rs-2507288/v1
