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Comprehensive Validation of Diagnostic Next-Generation Sequencing Panels for Acute Myeloid Leukemia Patients.
Wagner, Ulrich; Wong, Christine; Camenisch, Ulrike; Zimmermann, Kathrin; Rechsteiner, Markus; Valtcheva, Nadejda; Theocharides, Alexandre; Widmer, Corinne C; Manz, Markus G; Moch, Holger; Wild, Peter J; Balabanov, Stefan.
Afiliação
  • Wagner U; Department of Pathology and Molecular Pathology, University Hospital and University of Zurich, Zurich, Switzerland.
  • Wong C; Department of Pathology and Molecular Pathology, University Hospital and University of Zurich, Zurich, Switzerland.
  • Camenisch U; Department of Pathology and Molecular Pathology, University Hospital and University of Zurich, Zurich, Switzerland.
  • Zimmermann K; Division of Medical Oncology and Hematology, University Hospital and University of Zurich, Zurich, Switzerland.
  • Rechsteiner M; Department of Pathology and Molecular Pathology, University Hospital and University of Zurich, Zurich, Switzerland.
  • Valtcheva N; Department of Pathology and Molecular Pathology, University Hospital and University of Zurich, Zurich, Switzerland.
  • Theocharides A; Division of Medical Oncology and Hematology, University Hospital and University of Zurich, Zurich, Switzerland.
  • Widmer CC; Division of Medical Oncology and Hematology, University Hospital and University of Zurich, Zurich, Switzerland.
  • Manz MG; Division of Medical Oncology and Hematology, University Hospital and University of Zurich, Zurich, Switzerland.
  • Moch H; Department of Pathology and Molecular Pathology, University Hospital and University of Zurich, Zurich, Switzerland.
  • Wild PJ; Dr. Senckenberg Institute of Pathology, University Hospital Frankfurt, Frankfurt am Main, Germany; Frankfurt Institute for Advanced Studies, Frankfurt am Main, Germany; Wildlab, University Hospital Frankfurt MVZ GmbH, Frankfurt am Main, Germany. Electronic address: peter.wild@kgu.de.
  • Balabanov S; Division of Medical Oncology and Hematology, University Hospital and University of Zurich, Zurich, Switzerland. Electronic address: stefan.balabanov@usz.ch.
J Mol Diagn ; 24(8): 935-954, 2022 08.
Article em En | MEDLINE | ID: mdl-35718092
Next-generation sequencing has greatly advanced the molecular diagnostics of malignant hematological diseases and provides useful information for clinical decision making. Studies have shown that certain mutations are associated with prognosis and have a direct impact on treatment of affected patients. Therefore, reliable detection of pathogenic variants is critically important. Here, we compared four sequencing panels with different characteristics, from number of genes covered to technical aspects of library preparation and data analysis workflows, to find the panel with the best clinical utility for myeloid neoplasms with a special focus on acute myeloid leukemia. Using the Acrometrix Oncology Hotspot Control DNA and DNA from acute myeloid leukemia patients, panel performance was evaluated in terms of coverage, precision, recall, and reproducibility and different bioinformatics tools that can be used for the evaluation of any next-generation sequencing panel were tested. Taken together, our results support the reliability of the Acrometrix Oncology Hotspot Control to validate and compare sequencing panels for hematological diseases and show which panel-software combination (platform) has the best performance.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda / Transtornos Mieloproliferativos Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda / Transtornos Mieloproliferativos Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article