AMLVaran: a software approach to implement variant analysis of targeted NGS sequencing data in an oncological care setting.
Saved in:
| 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 |
|
Full text is not displayed to guests.
Login for full access.
|
|
| ISSN: | 17558794 |
|---|---|
| DOI: | 10.1186/s12920-020-0668-3 |