Identification of single nucleotide variants using position-specific error estimation in deep sequencing data

BACKGROUND: Targeted deep sequencing is a highly effective technology to identify known and novel single nucleotide variants (SNVs) with many applications in translational medicine, disease monitoring and cancer profiling. However, identification of SNVs using deep sequencing data is a challenging c...

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Detalles Bibliográficos
Autores principales: Kleftogiannis, Dimitrios, Punta, Marco, Jayaram, Anuradha, Sandhu, Shahneen, Wong, Stephen Q., Gasi Tandefelt, Delila, Conteduca, Vincenza, Wetterskog, Daniel, Attard, Gerhardt, Lise, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Technical Advance
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679440/
https://www.ncbi.nlm.nih.gov/pubmed/31375105
http://dx.doi.org/10.1186/s12920-019-0557-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679440/
https://www.ncbi.nlm.nih.gov/pubmed/31375105
http://dx.doi.org/10.1186/s12920-019-0557-9

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