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Team:ETHZ Basel/InformationProcessing/Visualization
From 2010.igem.org
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* activate or deactivate the controller | * activate or deactivate the controller | ||
* set the reference direction | * set the reference direction | ||
| - | * increase or decrease the threshold for cell detection (see [Team:ETHZ_Basel/InformationProcessing/CellDetection Cell Detection]) | + | * increase or decrease the threshold for cell detection (see [https://2010.igem.org/Team:ETHZ_Basel/InformationProcessing/CellDetection Cell Detection]) |
* alternatively, manually induce red or far-red light pulses of various length (instead of using the controllers provided in the toolbox). | * alternatively, manually induce red or far-red light pulses of various length (instead of using the controllers provided in the toolbox). | ||
If using a force-feedback joystick, the current swimming direction is furthermore given as a small force on the direction of the joystick, thus intuitively increasing the amount of information available for the user. | If using a force-feedback joystick, the current swimming direction is furthermore given as a small force on the direction of the joystick, thus intuitively increasing the amount of information available for the user. | ||
Revision as of 17:47, 26 October 2010
Visualization and Man-Machine Interface
Background
To control the E. lemming, the scientist has to be aware of a huge amount of information, which has to be visualized to him in real-time. Only with this information he or she is able to choose an E. coli cell to control, decide on a reference direction, and interfere in the experiments. This information include
- the current microscopy image
- all detected, not detected and falsely detected cells
- the selected cell itself
- its swimming direction
- the reference direction
- its path
- movements of the stage.
Since this information has to be absorbed by the experimentalist at a rate higher than three frames per second, a textual representation is not adequate. We thus decided to represent the information in an intuitive way by incorporating it into the microscope images.
To enable the scientist to interfere with the experiment without having to interrupt it, thus possibly loosing the currently controlled cell, we established two input devices: The user can either control the experiment and the E. lemming using the keyboard or the joystick. With both devices they can:
- select a cell to control
- activate or deactivate the controller
- set the reference direction
- increase or decrease the threshold for cell detection (see Cell Detection)
- alternatively, manually induce red or far-red light pulses of various length (instead of using the controllers provided in the toolbox).
If using a force-feedback joystick, the current swimming direction is furthermore given as a small force on the direction of the joystick, thus intuitively increasing the amount of information available for the user.
Both, the visual representation of the current state of the experiment as well as the user input had to be designed to require low computational efforts to not unnecessarily slow down the imaging.
User Experience
Visual Enhancements
All detected cells in the microscope image are highlighted by letting them glow blue (see example picture). The user can select a cell to control with the joystick or the keyboard, which is then glowing yellow instead of blue. The current swimming direction is indicated by a transparent yellow light cone, imitating the floodlight of cars or a flashlight, and the reference direction is depicted as a transparent red line. The path the cell has passed during the experiment is marked by small yellow dots, similar to footprints in snow. Finally, the automatic movement of the stage of the microscope when following a cell which swims out of the current field of view is indicated by arrows in the direction of movement, which are shortly popping up.
