Identification and Interpretation of Clinically Relevant Somatic Variants from Whole-Genome Sequencing Data

Maqbool K, Hassan Foroughi-Asl H, Ashwini Jeggari A, Ivanchuk V, Eisfeldt J, Renevey A, Elhami K, Rasi C, Nilsson D, Heinäniemi M, Lohi O, Wirta V

Blood 140 (Supplement 1) 13003-13004 [2022-11-15; online 2022-11-15]

DOI 10.1182/blood-2022-163295

Crossref 10.1182/blood-2022-163295


Publications 9.5.1