Defining Imaging Settings

Imaging Settings contain imaging instructions about when and how to image an experiment plate. This topic explains how to create a new imaging setting.

Adding a New Imaging Setting

Open the Imaging node on the Explorer and double-click Imaging Settings.

Imaging Settings

Right-click the Imaging Settings table and select Add. A new row will appear at the bottom of the list.

Add Imaging Settings

Click in the new row and type a name for the imaging setting.
At the right of the Imaging Settings table is a list of available imagers. Select whether the imaging setting should be disabled or available for either Visible, Ultraviolet, or SONICC imaging methods by clicking the corresponding option. See Imaging Setting below for more information.
OPTIONAL: To adjust settings for various optics and camera controls, select the desired control. Once you select the desired control, you will be able to modify the related setting.
OPTIONAL: Use the table below as a guide to modify the Image Tuning settings.

Title	Options
Leveling Mode	Off No window leveling will be applied.
	Manual The Manual mode lets you set the leveling window manually by defining its lower and upper level limits. The Lower level limit of leveling window defines the boundary below which all tonal values will be discarded from the image. The Upper level limit defines the boundary above which all tonal values will be discarded from the image.
	Auto The Auto mode automatically sets the leveling window according to low and high thresholds. The Low threshold is the percentage of pixels omitted at the left side of the image histogram before setting the lower limit of the tonal range. The High threshold is the percentage of pixels omitted at the right side of the image histogram after setting the upper limit of the tonal range. Auto-leveling has following two modes. Apply per drop applies window leveling to each image according to image’s own histogram. Apply per inspection applies window leveling to each image according to aggregate histogram of images currently being shown. This keeps the relative contrast the same between images currently being shown.

Enabling/Disabling Imaging Settings

You can enable or disable imaging settings by selecting or clearing the check boxes in the Enabled column from the Imaging Settings node in the Imaging folder on the Explorer. Once an Imaging Setting has been disabled, it will not display as an option on the Experiment page when you are defining the Image Schedule.

Imaging Setting Name

Configuring Optics and Camera Controls

When you add a new imager, you can define several different fields. Some of these fields will show up for certain imagers, some will not.

Optics Control	Description
Condenser	This value indicates the position of the condenser, expressed as the percentage at which the condenser's iris is closed. The condenser collects light from the Kohler light source and concentrates it onto the well being imaged. Values range from 0 – 100%. At 0%, the iris is fully open, and the cone of light is concentrated at a wide angle. At 100%, the iris is closed, and the light is concentrated in a column, rather than a cone. Hint: Higher condenser values provide greater shadowing around crystals and precipitates in the drop, thereby making them easier to see in the captured image.
Polarizer	This value tells you the angle, from 0 to 360 degrees, of the polarizer lens through which the light source is projected. A proper polarizer setting can help generate sufficient contrast in the captured image.
Dark Field	This percentage indicates the current brightness of the dark field illumination source that passes through a drop from above. At 0%, the light is turned off, and at 100% the light is at maximum brightness. With dark field illumination, light is scattered throughout the specimen under the microscope so that the specimen appears luminous against a dark background.

Camera Control	Description
Exposure	The exposure setting can be applied in one of the three following ways: Drop – With Drop selected, Rock Imager's auto-focus algorithm will be run on each drop of the plate. This algorithm will determine the ideal settings for the exposure time and bright field for each drop. Plate – With Plate selected, auto-focus will be run only on the first drop of the plate. The determined exposure time and bright field settings will then be used to image every drop on the plate. Fixed – With Fixed selected, auto-focus is turned off, and all drops are imaged using the exposure time and bright field settings that you specify. Exposure Time The exposure time is amount of time, in milliseconds, that the camera’s shutter remains open when capturing an image. This determines the amount of light allowed to fall on the camera's sensor. Bright Field This value sets the brightness level of the bright-field illumination source that passes through the drop from below. At 0%, the light is turned off, and at 100% the light is at maximum brightness. With bright-field illumination, light is passed through the specimen under the microscope so that the specimen appears dark against a bright background.
Gamma	Gamma affects the contrast of the midtones of the image. When you modify this setting, only the midtones are affected, without affecting black and white.
Resolution	The resolution is the size of the image in megapixels. To change the resolution, click the drop-down box and select a new resolution.

Defining Imaging Settings

Adding a New Imaging Setting

Enabling/Disabling Imaging Settings

Configuring Optics and Camera Controls

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