Clinically actionable cancer somatic variants (CACSV): a tumor interpreted dataset for analytical workflows

BACKGROUND: The recent development and enormous application of parallel sequencing technology in oncology has produced immense amounts of cell-specific genetic information. However, publicly available cell-specific genetic variants are not explained by well-established guidelines. Additionally, cell...

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Detalles Bibliográficos
Autores principales: Sobahy, Turki M., Tashkandi, Ghassan, Bahussain, Donya, Al-Harbi, Raneem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Technical Advance
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036759/
https://www.ncbi.nlm.nih.gov/pubmed/35468810
http://dx.doi.org/10.1186/s12920-022-01235-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036759/
https://www.ncbi.nlm.nih.gov/pubmed/35468810
http://dx.doi.org/10.1186/s12920-022-01235-7

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