AMLVaran: a software approach to implement variant analysis of targeted NGS sequencing data in an oncological care setting

BACKGROUND: Next-Generation Sequencing (NGS) enables large-scale and cost-effective sequencing of genetic samples in order to detect genetic variants. After successful use in research-oriented projects, NGS is now entering clinical practice. Consequently, variant analysis is increasingly important t...

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Detalles Bibliográficos
Autores principales: Wünsch, Christian, Banck, Henrik, Müller-Tidow, Carsten, Dugas, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7001226/
https://www.ncbi.nlm.nih.gov/pubmed/32019565
http://dx.doi.org/10.1186/s12920-020-0668-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7001226/
https://www.ncbi.nlm.nih.gov/pubmed/32019565
http://dx.doi.org/10.1186/s12920-020-0668-3

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