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

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Title: AMLVaran: a software approach to implement variant analysis of targeted NGS sequencing data in an oncological care setting.
Authors: Wünsch, Christian1 (AUTHOR) c.wuensch@uni-muenster.de, Banck, Henrik1 (AUTHOR), Müller-Tidow, Carsten2 (AUTHOR), Dugas, Martin1 (AUTHOR)
Source: BMC Medical Genomics. 2/4/2020, Vol. 13 Issue 1, p1-17. 17p.
Database: Academic Search Ultimate
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  Data: <searchLink fieldCode="JN" term="%22BMC+Medical+Genomics%22">BMC Medical Genomics</searchLink>. 2/4/2020, Vol. 13 Issue 1, p1-17. 17p.
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        Value: 10.1186/s12920-020-0668-3
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