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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2023
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| 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 |