Identification of Structural Variation from NGS-Based Non-Invasive Prenatal Testing

Copy number variants (CNVs) are an important type of human genome variation, which play a significant role in evolution contribute to population diversity and human genetic diseases. In recent years, next generation sequencing has become a valuable tool for clinical diagnostics and to provide sensit...

Descripción completa

Detalles Bibliográficos
Autores principales: Pös, Ondrej, Budis, Jaroslav, Kubiritova, Zuzana, Kucharik, Marcel, Duris, Frantisek, Radvanszky, Jan, Szemes, Tomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769840/
https://www.ncbi.nlm.nih.gov/pubmed/31500242
http://dx.doi.org/10.3390/ijms20184403

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769840/
https://www.ncbi.nlm.nih.gov/pubmed/31500242
http://dx.doi.org/10.3390/ijms20184403

Ejemplares similares