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Fluorescence Reconstruction Resources:

All source code for this project can be found in the folder entitled "Code_For_Distribution", along with the User Manual. The User Manual contains instructions for training and testing a U-Net and processing new data.


For the fastest introduction to applying the U-Net model with pre-trained weights, please see our demo Jupyter notebook at this link:

https://github.com/CohenLabPrinceton/Fluorescence-Reconstruction/tree/master/How_To_Use_The_Model


If you want to quickly train a new model with your own data without thinking about the code too much, please see the folder:

https://github.com/CohenLabPrinceton/Fluorescence-Reconstruction/tree/master/Lab_FRM

There, you will be able to run a single Python script (called "main.py") which will process the data and train/test the model. A second script (called "process_new_images.py") will enable you to use that trained model on new test images.


Our complete testing dataset, along with corresponding reconstructed images, can be found at:

http://doi.org/10.5281/zenodo.3783678


If you prefer a smaller dataset for rapid testing, we provide subsets of some of our data at the sources below.

A sample dataset for testing our code may be found at:

http://arks.princeton.edu/ark:/88435/dsp019w032593v

This DataSpace location contains a set of 1,000 matched image pairs from our keratinocyte dataset, imaged at 10x magnification. Phase contrast images (input) are paired with fluorescent images (output) of Hoechst 33342-stained nuclei, as imaged in DAPI.

Users may alternatively examine a sample dataset of MDCK cells, imaged at 20x:

http://arks.princeton.edu/ark:/88435/dsp019880vt87x

Here, DIC images (input) and paired with fluorescent images (output) corresponding to either nuclei or E-cadherin cell-cell junctions.


Users may find pre-trained weights for our standard U-Net implementation in the folder entitled "Pretrained_Weights". The README in that folder indicates which weights correspond to which experimental condition.

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