Human Exome Sequencing and Prospects for Predictive Medicine: Analysis of International Data and Own Experience

Today, whole-exome sequencing (WES) is used to conduct the massive screening of structural and regulatory genes in order to identify the allele frequencies of disease-associated polymorphisms in various populations and thus detect pathogenic genetic changes (mutations or polymorphisms) conducive to...

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Detalles Bibliográficos
Autores principales: Glotov, Oleg S., Chernov, Alexander N., Glotov, Andrey S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10455459/
https://www.ncbi.nlm.nih.gov/pubmed/37623486
http://dx.doi.org/10.3390/jpm13081236

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10455459/
https://www.ncbi.nlm.nih.gov/pubmed/37623486
http://dx.doi.org/10.3390/jpm13081236

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