| Literature DB >> 32150880 |
Francesco La Rocca1, Vitina Grieco1, Vitalba Ruggieri2, Emanuela Zifarone3, Oreste Villani4, Pietro Zoppoli2, Sabino Russi2, Simona Laurino2, Geppino Falco5,6, Giovanni Calice2, Anna Marinaccio7, Maria Iole Natalicchio7, Francesco Albano8, Pellegrino Musto8.
Abstract
JAK2 V617F mutational status is an essential diagnostic index in myeloproliferative neoplasms (MPNs). Although widely used for detection of JAK2 V617F mutation in peripheral blood (PB), sensitive real-time quantitative PCR (qPCR) presents some methodological limitations. Recently, emerging alternative technologies, like digital droplet PCR (ddPCR), have been reported to overcome some of qPCR's technical drawbacks. The purpose of this study was to compare the diagnostic utility of ddPCR to qPCR for JAK2 V617F detection and quantification in samples from MPNs patients. Sensitivity and specificity of qPCR and ddPCR in the detection of the mutation were assessed by using a calibrator panel of mutated DNA on 195 JAK2 positive MPN samples. Based on our results, ddPCR proved to be a suitable, precise, and sensitive method for detection and quantification of the JAK2 V617F mutation.Entities:
Keywords: JAK2; droplet digital PCR; myeloproliferative neoplasms; qPCR
Year: 2020 PMID: 32150880 DOI: 10.3390/diagnostics10030143
Source DB: PubMed Journal: Diagnostics (Basel) ISSN: 2075-4418