Cite
HARVARD Citation
Münz, M. et al. (2015). CSN and CAVA: variant annotation tools for rapid, robust next-generation sequencing analysis in the clinical setting. Genome medicine. 7 (1), pp. 1-8. [Online].
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Münz, M. et al. (2015). CSN and CAVA: variant annotation tools for rapid, robust next-generation sequencing analysis in the clinical setting. Genome medicine. 7 (1), pp. 1-8. [Online].