Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

BACKGROUND: Exome and genome sequencing are the predominant techniques in the diagnosis and research of genetic disorders. Sufficient, uniform and reproducible/consistent sequence coverage is a main determinant for the sensitivity to detect single-nucleotide (SNVs) and copy number variants (CNVs). H...

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Detalles Bibliográficos
Autores principales: Yaldiz, Burcu, Kucuk, Erdi, Hampstead, Juliet, Hofste, Tom, Pfundt, Rolph, Corominas Galbany, Jordi, Rinne, Tuula, Yntema, Helger G., Hoischen, Alexander, Nelen, Marcel, Gilissen, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10155375/
https://www.ncbi.nlm.nih.gov/pubmed/37138343
http://dx.doi.org/10.1186/s40246-023-00485-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10155375/
https://www.ncbi.nlm.nih.gov/pubmed/37138343
http://dx.doi.org/10.1186/s40246-023-00485-5

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