2016 Synthetic Biology: Engineering, Evolution & Design (SEED)
Minimum Flow Cytometry Calibration Information (MinFlowCal)
Authors
Jacob Beal - Presenter, Raytheon BBN Technologies
Peter McLean, NIST
Traci Haddock-Angelli, Boston University
Brian Teague, MIT
Matthew S. Munson, National Institute of Standards and Technology
Sarah Munro, National Institute of Standards and Technology
Marc Salit, Joint Initiative for Metrology in Biology
Flow cytometry is a powerful method for inspection of the behavior of large numbers of individual cells in a population. However, in the absence of appropriate data processing, calibration, and sufficient reporting, measurement results obtained with a flow cytometer are difficult to interpret or compare to existing datasets. MinFlowCal is a Synthetic Biology Standards Consortium (SBSC) project aimed at addressing these issues by delineating a minimum-information standard and calibration method that will facilitate appropriate reporting of flow cytometry data. We describe the use of commercially available fluorescent beads to calibrate fluorescence signal values to a common fluorescence unit, e.g., mean equivalent fluorochrome (MEF). Adopting and reporting calibrated flow cytometry measurement results will enable comparability and evaluation of reproducibility across instrument platforms and laboratories.