Process, visualize, model parameters to raw intensities from single cell timelapse fluorescence microscopy recordings captured by ImageJ. It is meant to automate downstream analysis of tandem fluorescent tags to determine protein stability. This package is borne out of my NST part II pharmacology research project, under Lindon laboratory, Department of Pharmacology, Cambridge. Mathematical modelling is obtained from Khmelinskii A, Keller PJ, Bartosik A, Meurer M, Barry JD, Mardin BR, Kaufmann A, Trautmann S, Wachsmuth M, Pereira G, Huber W, Schiebel E, Knop M. Tandem fluorescent protein timers for in vivo analysis of protein dynamics. Nat Biotechnol. 2012 Jun 24;30(7):708-14. doi: 10.1038/nbt.2281. PMID: 22729030.
Package details |
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Maintainer | Chang Jia Geng <jgc47@cam.ac.uk> |
License | MIT + file LICENSE |
Version | 0.1.0 |
Package repository | View on GitHub |
Installation |
Install the latest version of this package by entering the following in R:
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