Clinical-grade validation of whole genome sequencing reveals robust detection of low-frequency variants and copy number alterations in CLL
- Jenny Klintman
- , Katerina Barmpouti
- , Samantha J.L. Knight
- , Pauline Robbe
- , Hélène Dreau
- , Ruth Clifford
- , Kate Ridout
- , Adam Burns
- , Adele Timbs
- , David Bruce
- , Pavlos Antoniou
- , Alona Sosinsky
- , Jennifer Becq
- , David Bentley
- , Peter Hillmen
- , Jenny C. Taylor
- , Mark Caulfield
- , Anna H. Schuh
- University of Oxford
- Oxford University Hospitals NHS Foundation Trust
- NIHR Oxford Biomedical Research Centre
- University Hospitals Limerick
- Genomics England
- Illumina
- Leeds Teaching Hospitals NHS Trust
Research output: Contribution to journal › Article › peer-review