Flanking monomer repeats define lower context complexity of sites containing single nucleotide polymorphisms in the human genome

We have investigated a mutation frequency within the human genome for the set of known single nucleotide polymorphisms (SNPs) from the “1000 genomes” project. We have developed and applied novel statistical computational methods to analyze genetic text based on its complexity. A complexity profiling...

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Detalhes bibliográficos
Principais autores: N. S. Safronova, M. P. Ponomarenko, I. I. Abnizova, G. V. Orlova, I. V. Chadaeva, Y. L. Orlov
Formato: Artigo
Idioma:English
Publicado em: Siberian Branch of the Russian Academy of Sciences, Federal Research Center Institute of Cytology and Genetics, The Vavilov Society of Geneticists and Breeders 2016-01-01
coleção:Вавиловский журнал генетики и селекции
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Acesso em linha:https://vavilov.elpub.ru/jour/article/view/483