PyFDAP is a Python-based analysis framework for Fluorescence Decay After Photoconversion (FDAP) experiments.
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Updated
Jan 27, 2017 - Python
PyFDAP is a Python-based analysis framework for Fluorescence Decay After Photoconversion (FDAP) experiments.
ImageJ macros that automate the workflow of thresholding and analyzing the size and intensity of objects/regions in microscope images.
This is the start of a major spectroscopy absorption and emission data base. These are going to be all of my spectral and lab data files from all my experiments from my spectrometer prototypes from Hackaday.com
Code for spectral separation for Fiber based spectral FLIM project
Quantitation of migration of fluorescent spots into regions of interest.
ImageJ Scripts for Microscope Images of Florescently Labled Cells
Lego based fluorescence microscope
fluorescence ultrasound modulated optical tomography with radiative transport equation.
Track Fluorescent Protein in Live Cell images with OpenCV
Super-resolution fluorescence microscopy by stepwise optical saturation
Saturation-compensated measurements for fluorescence lifetime imaging microscopy
Investigation of signal-to-noise ratio in frequency-domain multiphoton fluorescence lifetime imaging microscopy
A web tool for the analysis of Fluorescence Recovery After Photobleaching (FRAP) data.
Automatic segmentation of intravital fluorescence microscopy images by K-means clustering of FLIM phasors
Step-by-step instruction to quantify fluorescence intensities from timelapse imaging experiments
Bacterial chromosmal foci tracker.
Object Oriented Segmentation of Cell Nuclei in Fluorescence Microscopy Images
Real-time, interactive exploration of 3D image stacks
A MATLAB suite implementing computer vision pipeline to extract information from the noisy TIRF microscopy data (image stack)
Zebrafish embryo fluorescence quantification
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