This shows you the differences between two versions of the page.
| Both sides previous revision Previous revision Next revision | Previous revision |
| post:labelstartandendfluocells.m [2019/10/11 15:34] – pseudomoaner | post:labelstartandendfluocells.m [2019/10/23 12:22] (current) – pseudomoaner |
|---|
| |
| **Class:** Script | **Class:** Script |
| | |
| | **Dependancies:** [[post:meanintinellipse.m]] |
| |
| **Description:** Takes in the [[usage:tracking#outputs|procTracks]] data structure and a pair of fluorescence images, one taken at the beginning of the timeseries and one at the end. By only taking two fluorescence images, you can associate each of your tracks with a fluorescence-based population without causing excess phototoxicity or photobleaching. | **Description:** Takes in the [[usage:tracking#outputs|procTracks]] data structure and a pair of fluorescence images, one taken at the beginning of the timeseries and one at the end. By only taking two fluorescence images, you can associate each of your tracks with a fluorescence-based population without causing excess phototoxicity or photobleaching. |
| </code> | </code> |
| |
| **Example output:** Plot generated in the [[usage:plotting]] module, showing how fluorescence can be used to separate a motile (black) from a non-motile (red) population. | **Example output:** Plot generated in the [[usage:plotting]] module, showing how fluorescence can be used to separate a high motility (black) from a low-motility (red) genotype when mixed in a single system. |
| |
| {{ :post:speedsplitexample.png?nolink&400 |}} | {{ :post:speedsplitexample.png?nolink&400 |}} |
| |
| |