Main window

The main window is shared among all three pages.

It can visualize:

  • Image data (2D images, 3D volumes and Binaries) and
  • Results data (Tables, Graphs, Layouts, …)

The main window can display images and results coming from the same origin side-by-side in a dedicated Compare mode.

Image

Image overview
Main window: 2D image with cells

Toolbar
houses the major viewing modes, information overlays, zooming controls and menu More actions.
Image area
displays the image (with overlaid or split channels) or the volume. Both can show binary layers.
Statusbar
displays channels selection, information about the calibration, bit-depth and image size in pixels. If there are binary layers in the image it also has the buttons to show each of them and a settings dialog.
ND navigation
navigation bars are shown depending on the image dimensionality. Every dimension has ticks to move to an absolute position directly and navigation buttons for relative moves as well as the play button with options.

Split channels

Split channels
Main window: Split channels (Alexa 488 and Transmitted) with cells

Volume view

Volume view
Main window: 3D image with cells

LUTs

There are two LUTs controls Simple and Complex (can be changed in the settings) using different sliders to achieve the same result.

LUTs
Main window: Simple LUTs control

The resulting RGB pixel intensity is calculated from all channel intensities () transformed by the LUTs and mapped to their respective color () as follows:

The Gain slider () is logarithmic and is the major control of brightness. The Offset () controls the blacks and Gamma ()the contrast.

LUTs
Main window: LUTs control

The resulting RGB pixel intensity is calculated from all channel intensities () transformed by the LUTs and mapped to their respective color () as follows:

The Lo an Hi bounds define the Range that is mapped to minimum (0) and maximum (255) brightness and Gamma ()the contrast.

The sliders and histogram range can be zoomed to the actual data range using the button at the low-right of the window.

The Low and High percentiles are used when calculating auto-contrast in such a way that only the specified percent of pixels is under- or over- saturated. The Low and High is set separately for brightfield (BF) and fluorescence (Fluo).

Furthermore, when brightfield is mixed with fluorescence there is slider for Brightfield opacity.

The match intensity slider is for compare mode to bring the intensities of compared images more to look alike.

Image info

Image info
Main window: Image info

Binary layers

Binary layers

Individual Layers (here Nucleus and Cell) can be switched on/off directly from the statusbar. In the Binaries display settings it is further possible to:

  • change the layer position in the stack (drag it up or down by its name),
  • show/hide each layer,
  • override the color of each layer,
  • change the opacity of each layer independently,
  • show/hide object ID numbers in the image and
  • colorize object by ID

Results

Recipes can create results (tables, graphs, …) with different level of complexity.

Complex results
Main window: Image with complex results

The results can be organized into four layouts:

  • image with complex results where the window is divided into four quadrants,
  • image with simple results where the results are below the image,
  • image with simple results (vertical) where the results are left of the image or
  • just the image where the results are hidden.

There is also an automatic option which chooses the layout to show all results.

Simple results
Main window: Image with simple results
Simple results
Main window: Image with simple results (vertical)
image only
Main window: Image only

Compare mode

Images coming from the same original with or without results are opened together.

Open first images and from the More actions button open either Open all related results or select few specific ones one-by-one from Open related results dropdown.

Compare view
Main window: Compare view

Use the Compare view button to toggle a display where the images are

  • one over the other and
  • side-by-side

Multiple images side-by-side

In compare view these are synchronized:

  • the viewport of all images is synchronized to show the same portion of the image,
  • the channel selection is equal (where possible),
  • ND2 control is synchronized (where possible),
  • the LUTs settings are synchronized and
  • deconvolution info and scale bar are shown on all images.

Multiple images
Main window: Multiple images

Multiple volumes
Main window: Multiple volumes

Multiple results side-by-side

Multiple images with results
Main window: Multiple images with results