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Updated: May 22, 2026

qPCRTag Analysis - A High Throughput, Real Time PCR Assay for Sc2.0 Genotyping
Published on: May 25, 2015
Fast-mode duplex qPCR for BCR-ABL1 molecular monitoring: innovation, automation, and harmonization
Gareth Gerrard1, Katherine Mudge, Pierre Foskett
1Imperial Molecular Pathology, Imperial College Academic Health Science Centre, London, United Kingdom. g.gerrard@imperial.ac.uk
Abstract:
Reverse transcription quantitative polymerase chain reaction (RTqPCR)is currently the most sensitive tool available for the routine monitoring of disease level in patients undergoing treatment for BCRABL1 associated malignancies. Considerable effort has been invested at both the local and international levels to standardise the methodology and reporting criteria used to assess this critical metric. In an effort to accommodate the demands of increasing sample throughput and greater standardization, we adapted the current best-practice guidelines to encompass automation platforms and improved multiplex RT-qPCR technology.
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