Abstract
Light‐sheet fluorescence microscopy (LSFM) is a powerful technique that
can provide high‐resolution images of biological samples. Therefore,
this technique offers significant improvement for three‐dimensional (3D)
imaging of living cells. However, producing high‐resolution 3D images
of a single cell or biological tissues, normally requires high
acquisition rate of focal planes, which means a large amount of sample
sections. Consequently, it consumes a vast amount of processing time and
memory, especially when studying real‐time processes inside living
cells. We describe an approach to minimize data acquisition by
interpolation between planes using a phase retrieval algorithm. We
demonstrate this approach on LSFM data sets and show reconstruction of
intermediate sections of the sparse samples. Since this method
diminishes the required amount of acquisition focal planes, it also
reduces acquisition time of samples as well. Our suggested method has
proven to reconstruct unacquired intermediate planes from diluted data
sets up to 10× fold. The reconstructed planes were found correlated to
the original preacquired samples (control group) with correlation
coefficient of up to 90%. Given the findings, this procedure appears to
be a powerful method for inquiring and analyzing biological samples.
Original language | English |
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Article number | e202000035 |
Journal | Journal of Biophotonics |
Volume | Early View |
Early online date | 20 Apr 2020 |
DOIs | |
Publication status | E-pub ahead of print - 20 Apr 2020 |
Keywords
- Gerchberg-Saxton algorithm
- Light-sheet microscopy
- Super resolution