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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2020
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| Materias: | |
| 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 |