Accuracy and reproducibility of somatic point mutation calling in clinical-type targeted sequencing data

BACKGROUND: Treating cancer depends in part on identifying the mutations driving each patient’s disease. Many clinical laboratories are adopting high-throughput sequencing for assaying patients’ tumours, applying targeted panels to formalin-fixed paraffin-embedded tumour tissues to detect clinically...

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Detalles Bibliográficos
Autores principales: Karimnezhad, Ali, Palidwor, Gareth A., Thavorn, Kednapa, Stewart, David J., Campbell, Pearl A., Lo, Bryan, Perkins, Theodore J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7560075/
https://www.ncbi.nlm.nih.gov/pubmed/33059707
http://dx.doi.org/10.1186/s12920-020-00803-z

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