3D image stacks are routinely acquired to capture data that lie on undulating 3D manifolds yet processed in 2D by biologists. Algorithms to reconstruct the specimen morphology into a 2D representation from the 3D image volume are employed in such scenarios. In this paper, we present FastSME, which offers several improvements on the baseline SME algorithm which enables accurate 2D representation of data on a manifold from 3D volumes, however is computationally expensive. The improvements are achieved in terms of processing speed (3X-10X speed-up depending on image size), minimizing sensitivity to initialization, and also increases local smoothness of the recovered manifold resulting in better reconstructed 2D composite image. We compare the proposed FastSME against the baseline SME as well as other accessible state-of-the-art tools on synthetic and real microscopy data. Our evaluation on multiple metrics demonstrates the efficiency of the presented method in maintaining fidelity of manifold shape and hence specimen morphology.
To cite:
FastSME Codes (Matlab): https://github.com/Shihav/FastSME
FastSME Dataset: https://data.mendeley.com/datasets/bn7zbzc3gg/1
FastSME Poster: https://drive.google.com/open?id=1q6uuqkqd2FAba60ZGgmXZlO_iRl74xdd
FastSME Presentation: https://drive.google.com/open?id=1GOUgZ89DWaEG4lT_p2Aper6l8kYuaNEC
FastSME Paper: https://drive.google.com/open?id=1BIdjX7FX2HdKAj0ijtoQz8n1AZa78vQH
SME paper: https://www.nature.com/articles/ncomms15554
SME codes (Matlab and FIJI plugin): https://github.com/biocompibens/SME