Reducing cytogenetic testing in the era of next generation sequencing: Are we choosing wisely?
Eri KawataBenjamin D HedleyBenjamin Chin-YeeAnargyros XenocostasAlejandro Lazo-LangnerCyrus C HsiaKang Howson-JanPing YangMichael A LevyStephanie SantosPratibha BhaiChristopher HowlettHanxin LinMike KadourBekim SadikovicIan H Chin-YeePublished in: International journal of laboratory hematology (2021)
Utilizing NGS as the primary genomic testing modality NGS was feasible and well accepted, reducing over three quarters of all CG requests and improving the financial case for adoption of NGS. Key factors for the success of this study were collaboration of clinical and genomic diagnostic teams in developing the algorithm, rapid turnaround time for BM interpretation for triage, and communication between laboratories.