Clinical-grade validation of whole genome sequencing reveals robust detection of low-frequency variants and copy number alterations in CLL

Klintman J., Barmpouti K., Knight S., Robbe P., DREAU H., Clifford R., RIDOUT K., BURNS A., Timbs A., BRUCE D., Antoniou P., Sosinsky A., Becq J., Bentley D., Hillmen P., TAYLOR J., Caulfield M., SCHUH A.

DOI

10.1111/bjh.15406.

Type

Journal article

Journal

British Journal of Haematology

Publisher

Wiley

Publication Date

12/06/2019

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