The utility of next-generation sequencing in diagnosis and monitoring of acute myeloid leukemia and myelodysplastic syndromes

International Journal of Laboratory Hematology

Volumn 37, Issue S1, 2015, Pages 115-121

  Duncavage, E J ^a   Tandon, B ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Acute myeloid leukemia; Clinical diagnostics; Minimal residual disease; Myelodysplastic syndrome; Next generation sequencing

Indexed keywords

ACUTE MYELOBLASTIC LEUKEMIA; ASXL1 GENE; CANCER PATIENT; CANCER PROGNOSIS; CEBPA GENE; CLINICAL LABORATORY; CYTOGENETICS; DIAGNOSTIC VALUE; ETV6 GENE; EXOME; EZH2 GENE; FLT3 GENE; GENE; GENE MUTATION; HUMAN; MORBIDITY; MORTALITY; MYELODYSPLASTIC SYNDROME; NEXT GENERATION SEQUENCING; NPM1 GENE; PATIENT MONITORING; PRIORITY JOURNAL; REVIEW; RUNX1 GENE; TUMOR SUPPRESSOR GENE; ACUTE DISEASE; GENETIC PREDISPOSITION; GENETICS; HIGH THROUGHPUT SEQUENCING; LEUKEMIA, MYELOID; MUTATION; MYELODYSPLASTIC SYNDROMES; PROCEDURES; PROGNOSIS; REPRODUCIBILITY; SENSITIVITY AND SPECIFICITY;

ACUTE DISEASE; GENETIC PREDISPOSITION TO DISEASE; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; LEUKEMIA, MYELOID; MUTATION; MYELODYSPLASTIC SYNDROMES; PROGNOSIS; REPRODUCIBILITY OF RESULTS; SENSITIVITY AND SPECIFICITY;

EID: 84929302331     PISSN: 17515521     EISSN: 1751553X     Source Type: Journal    
DOI: 10.1111/ijlh.12361     Document Type: Review

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