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

British Journal of Haematology, EarlyView.

Source: British Journal of Haematology - May 29, 2018 Category: Hematology Authors: Jenny Klintman , Katerina Barmpouti , Samantha J. L. Knight , Pauline Robbe , H élène Dreau , Ruth Clifford , Kate Ridout , Adam Burns , Adele Timbs , David Bruce , Pavlos Antoniou , Alona Sosinsky , Jennifer Becq , David Bentl Source Type: research