Publication
Tomographic phase microscopy (TPM) in flow cytometry is one of the most promising computational imaging techniques for the quantitative 3-dimensional (3D) analysis of unstained single cells. Continuous cells' flow, combined with the stain-free mode, can assure the high-throughput collection of quantitative and informative 3D data. TPM promises to allow rapid cells' screening by a nondestructive technique and with statistically relevant data. The current leading-edge research aimed at developing TPM systems in flow cytometry has already demonstrated the possibility of acquiring thousands of single-cell tomograms. Nevertheless, a key unsolved problem exists about the efficient storage and easy handling of such a huge amount of 3D data that prevents rapid analysis for cell diagnosis. Here, we show, for the first time, an effective encoding strategy of single-cell tomograms that can completely overcome this critical bottleneck. Essentially, by using the 3D version of Zernike polynomials, we demonstrate that the 3D refractive index distribution of a cell can be straightforwardly encoded in 1D with negligible information loss (