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

Research output: Contribution to journal › Article › peer-review

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Biochemistry, Genetics and Molecular Biology