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Paper Details

Clinical-grade validation of whole genome sequencing reveals robust detection of low-frequency variants and copy number alterations in CLL.
Br J Haematol
15
2018
CLL, TP53 variants, chronic lymphocytic leukaemia, genome-wide single nucleotide polymorphism array, insertion/deletions, patients
Author NameAffiliation
David R Bentley
David R Bentley
Jenny C TaylorNIHR Biomedical Research Centre, University of Oxford
Jenny C TaylorOxford Biomedical Research Centre
Mark J CaulfieldUniversity Hospital Limerick
Mark J CaulfieldUniversity Hospital Limerick
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