iPSC/SYTO24/PhalloidinAF568 on 96-well plate; computational quantitative phase.
Antony C Chan

folder 2019-09-19-hiPSC-SYTO24-PhalloidinAF568 (8 files)
fileLICENSE.txt 1.58kB
filemetadata.xml 1.99kB
filefluorescence_raw.png 80.01kB
filefpm_restored.png 137.78kB
filebrightfield_raw.png 118.71kB
filedecode.py 5.11kB
file2019-09-19-hiPSC-SYTO24-PhalloidinAF568.recon.hdf5 3.85GB
file2019-09-19-hiPSC-SYTO24-PhalloidinAF568.raw.hdf5 19.17GB
Type: Dataset
Tags: quantitative phase, 96 wells, high-throughput screening, iPSC, Fourier Ptychography, FPM, fluorescence

Bibtex:
@article{,
title= {iPSC/SYTO24/PhalloidinAF568 on 96-well plate; computational quantitative phase.},
journal= {},
author= {Antony C Chan},
year= {2019},
url= {http://dx.doi.org/10.1038/s41598-019-47146-z},
abstract= {Complete dataset of the brightfield, darkfield, digital quantitative phase, and widefield fluorescence z-stack images of iPSC culture on the 96-well plate, captured by the Caltech parallel ptychographic imaging system (codename: 96 Eyes). The cell culture is stained with SYTO24 and PhalloidinAF568 for the proof of concept.

Also attached are the preview images in PNG format, as well as a minimal Python code to decode the raw data files.

Published in: A.C.S. Chan, J Kim, A Pan, H Xu, D Nojima, C Hale, S Wang, C Yang, "Parallel Fourier ptychographic microscopy for high-throughput screening with 96 cameras (96 Eyes)" Scientific Reports 9, 11114 (2019). http://dx.doi.org/10.1038/s41598-019-47146-z

Preprint: https://www.biorxiv.org/content/10.1101/547265v2

It is recommend that the raw pixels to be decoded on demand; otherwise it is not practical to load all >20GB data to computer memory just to crop the images later. Read the attached Python script `decoded.py` to learn how to select the region of interest (ROI) in-place to reduce the disk read/write time.

For Matlab users, on-demand pixel readout can be done with the `h5read` function. Try out the following pseudo-code, and debug accordingly to read all FPM raw pixels.

```matlab
fpm_raw = h5read('path/to/filename.h5', '/imlow', [1,1,well_id, 1], [512, 512, 1, 49]);
```

Reference implementation of the Fourier Ptychographic microscopy (FPM) phase-channel reconstruction algorithm, written in Halide the 4th generation coding language, will be published at:
https://github.com/antonysigma/fpm-96eyes-pipeline

},
keywords= {quantitative phase, 96 wells, high-throughput screening, iPSC, Fourier Ptychography, FPM, fluorescence},
terms= {Copyright (c) 2019, Antony C. S. Chan and Changhuei Yang
California Institute of Technology
Pasadena, CA, USA.

Redistribution and use in source and binary forms, with or without
modification, are permitted provided that the following conditions are met:

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THIS SOFTWARE IS PROVIDED BY THE COPYRIGHT HOLDERS AND CONTRIBUTORS "AS IS"
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CAUSED AND ON ANY THEORY OF LIABILITY, WHETHER IN CONTRACT, STRICT LIABILITY,
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OF THIS SOFTWARE, EVEN IF ADVISED OF THE POSSIBILITY OF SUCH DAMAGE.},
license= {BSD 3-clause license},
superseded= {}
}


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