fit2x is currently in early development.

fit2x is a collection of models that use maximum likelihood estimators for polarization and time-resolved fluorescence decays.

fit2x implement burst integrated fluorescence lifetime fits (BIFL) with scatter. The library can be used in conjuncture with tttrlib to analyze and process single-molecule FRET (smFRET) experiments and confocal laser scanning microscopy (CLSM) data. The fit2x shared libary can be used from LabView and is wrapped by SWIG (Simplified Wrapper and Interface Generator) for common scripting languages as Python as main target language.

• Low memory footprint (keep objective large datasets, e.g. FLIM in memory).
• Platform independent C/C++ library with interfaces for scripting libraries

• Polarization and time-resolved analysis
• Stable analysis results with minimum photon counts
• Robust and thoroughly tested maximum likelihood estimators

import fit2x
import numpy as np

irf = np.array(
    [0, 0, 0, 260, 1582, 155, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0,
     0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 22, 1074, 830, 10, 0, 0,
     0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 
     0, 0], dtype=np.float64
)

data = np.array(
    [0, 0, 0, 1, 9, 7, 5, 5, 5, 2, 2, 0, 0, 0, 0, 0, 1, 0, 0, 0, 0, 0, 
     0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 3, 2, 2, 2, 2, 3, 0, 1, 0,
     1, 1, 1, 2, 0, 0, 0, 0, 1, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0]
)

settings = {
    'dt': 0.5079365079365079,
    'g_factor': 1.0,
    'l1': 0.1,
    'l2': 0.2,
    'convolution_stop': 31,
    'irf': irf,
    'period': 16.0,
    'background': np.zeros_like(irf)
}
fit23 = fit2x.Fit23(**settings)

# initial values
tau, gamma, r0, rho = 2.2, 0.01, 0.38, 1.22
x0 = np.array([tau, gamma, r0, rho])
fixed = np.array([0, 1, 1, 0])
# pass data and initial values to fit. 
# The return value contains the fit result 
r = fit23(
    data=data,
    initial_values=x0,
    fixed=fixed
)

Pure pure C/C++ high performance algorithms for analysis of low photon count data.

The C++ shared library can be installed from source with cmake:

git clone --recursive https://github.com/fluorescence-tools/fit2x.git
mkdir fit2x/build; cd fit2x/build
cmake ..
sudo make install

The Python bindings can be either be installed by downloading and compiling the source code or by using a precompiled distribution for Python anaconda environment.

The following commands can be used to download and compile the source code:

git clone --recursive https://github.com/fluorescence-tools/fit2x.git
cd fit2x
sudo python setup.py install

In an anaconda environment the library can be installed by the following command:

conda install -c tpeulen fit2x

For most users the latter approach is recommended. Currently, pre-compiled packages for the anaconda distribution system are available for 64bit Windows, macOS, and Linux.

Legacy 32-bit platforms and versions of programming languages, e.g, Python 2.7 are not supported.

The API of fit2x as well as some use cases are documented on its web page

In case you notice unusual behaviour do not hesitate to contact the authors.

fit2x was developed at the Seidel Lab (Heinrich Heine University). and is maintained by Thomas Peulen. fit2x is released under the open source MIT license.

If you have used fit2x in a scientific publication, we would appreciate citations to the following paper:

Michael Maus, Mircea Cotlet, Johan Hofkens, Thomas Gensch, Frans C. De Schryver, J. Schaffer, and C. A. M. Seidel, 2001. An Experimental Comparison of the Maximum Likelihood Estimation and Nonlinear Least-Squares Fluorescence Lifetime Analysis of Single Molecules. Anal. Chem., 73, 9, pp2078–2086.