Ultra-deep multi-oncopanel sequencing of benchmarking samples with a wide range of variant allele frequencies

The lack of suitable reference genomic material to enable a transparent cross-lab study of oncopanels inspired the SEQC2 Oncopanel Sequencing Working Group to develop four reference samples, sequenced with eight oncopanels at independent test laboratories with ultra-deep sequencing depth. This rich,...

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Detalles Bibliográficos
Autores principales: Gong, Binsheng, Kusko, Rebecca, Jones, Wendell, Tong, Weida, Xu, Joshua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Data Descriptor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184574/
https://www.ncbi.nlm.nih.gov/pubmed/35680918
http://dx.doi.org/10.1038/s41597-022-01359-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184574/
https://www.ncbi.nlm.nih.gov/pubmed/35680918
http://dx.doi.org/10.1038/s41597-022-01359-6

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