qFADDpy
qFADDpy implements the Q-FADD method to quantify recruitment kinetics of fluorescently labeled DNA repair proteins to laser-induced DNA damage sites for analysis of diffusion and accumulation dynamics.
Key Features:
- Q-FADD implementation: Implements the Quantitation of Fluorescence Accumulation after DNA Damage (Q-FADD) approach to extract kinetic parameters from fluorescence accumulation data.
- Automated preprocessing: Performs preprocessing including corrections for nuclear drift to improve accuracy of time-series fluorescence measurements.
- Automated grid-search fitting: Uses an automated grid-search algorithm to identify best-fit model parameters for protein recruitment dynamics.
- Simulation of replicates: Integrates automated simulation of replicates within the grid-search to support statistical assessment of fits.
- Monte Carlo diffusion modeling: Applies Monte Carlo diffusion models to interpret recruitment timescales and diffusion-related behavior of repair proteins.
Scientific Applications:
- DNA damage response kinetics: Quantifies accumulation, action, and dissipation timescales of repair proteins at sites of DNA damage, including examples such as PARP1.
- Protein recruitment and diffusion analysis: Compares recruitment kinetics and diffusion properties of repair proteins to elucidate interactions within genome maintenance networks.
Methodology:
Automated preprocessing with nuclear drift correction, automated grid-search fitting incorporating simulated replicates, and Monte Carlo diffusion models.
Topics
Details
- License:
- MIT
- Tool Type:
- library, web application
- Programming Languages:
- Python
- Added:
- 11/29/2021
- Last Updated:
- 11/29/2021
Operations
Publications
Bowerman S, Mahadevan J, Benson P, Rudolph J, Luger K. Automated Modeling of Protein Accumulation at DNA Damage Sites using qFADD.py. Unknown Journal. 2021. doi:10.1101/2021.03.15.435501.
Links
Repository
https://github.com/Luger-Lab/Q-FADDIssue tracker
https://github.com/Luger-Lab/Q-FADD/issues