- Viewing Projection Data
- Gene Search
Brain Explorer® 3-D Viewer is an application for viewing brain anatomy, gene expression and fluorescence projection data in three dimensions in the framework of the Allen Reference Atlas.
Using Brain Explorer, you can:
• View a fully interactive version of the Allen Reference Atlas in 3-D.
• View gene expression data in 3-D at 200 µm3 resolution.
• View projection data in 3-D at 100 µm3 resolution.
• View expression data and projection data from multiple experiments superimposed on each other in 3-D.
• Navigate the high-resolution 2-D ISH and projection images using the 3-D model.
• Link to associated gene metadata on the Allen Mouse Brain Atlas web application.
• Operating System: Microsoft Windows 7
• CPU: Intel Core Duo or AMD 1.8GHz
• System Memory: 1GB
• Graphics Card: Hardware 3D OpenGL accelerated AGP or PCI Express with 64MB RAM
• Screen: 1024x768, 32-bit true color
• Hard Disk: 200MB free space
Note: Brain Explorer is known to work with the following video chipsets: nVidia GeForce 9400/9600, nVidia Quadro FX 1800/3800/5600, AMD Radeon 9600, AMD Radeon HD 3200/4550, Intel Q35/Q45 Express.
For the best performance, please check with your video card vendor for the latest available drivers before using Brain Explorer. The Windows version of the Brain Explorer viewer is available here. Double-click the downloaded BrainExplorer2.msi file and follow the prompts.
• Operating System: OS X 10.6.8
• CPU: Intel 1.8GHz
• System Memory: 1GB
• Graphics Card: 3D-capable with 64MB RAM
• Screen: 1024x768, 32-bit millions of colors
• Hard Disk: 200MB free space
Note: Please install the latest system updates from Apple to ensure you have the latest video card drivers.
The Mac version of the Brain Explorer viewer is available here. Double-click the downloaded zip file to unpack Brain Explorer.
A one-time download containing anatomy files is needed following installation of the Brain Explorer application. The first time you open the Brain Explorer software, you will be asked to choose to download files for the Allen Developing Mouse and Allen Human Brain atlases. Click on the atlases you would like to use and then click the Install button.
To download missing atlases on the PC, go to the Help menu and select Download Atlases. On the Mac, the command is in the Brain Explorer 2 menu.
The Brain Explorer application will inform you when updates to the Brain Explorer application itself or its atlases are available. New data may not be available for viewing until you install the required updates.
To load projection data into the Brain Explorer viewer, go to the Allen Mouse Brain Connectivity Atlas and perform an efferent search. You can also select a structure name from the list of injection sites. Your search brings back a list of experiments. Click on a row to select an experiment of interest. A 3-D thumbnail of the projection data of that experiment will appear to the right. Click on the blue “View in 3D” file link to launch the Brain Explorer application.
The Image Viewer displays a 3-D representation of the neuronal projections in the selected experiment. Each sphere (when present) represents the injection site re-sampled to a 100 micron grid resolution. Each line traces fluorescent signal through the brain and each cube represents termination of signal. Larger polygons corresponds to a greater density of signal. Gene expression data can be displayed concurrently with the projection data. Gene expression will also be represented by spheres as described in here.
You can select a sphere or cube by clicking on it. Volumes can be deselected by clicking on blank space. The original projection section of the selected sphere/cube will be displayed blended with the projection segmentation in the lower left hand portion of the screen. The blending can be adjusted by selecting Image Controls from the View menu and moving the Image Blending slider. Clicking on the arrow in the projection image will open the corresponding image in a high resolution image viewer.
The information at the upper left corner of the main Brain Explorer window summarizes the fluorescent signal detected in the selected grid location. This information includes the primary injection site, the annotated location of the selected point, average signal density and intensity (over pixels) and the location. The Informatics Data Processing White Paper describes how the measurements were obtained.
To change the projection signal representation, click on the “Data” tab in the top left hand corner of your screen and select an option under “Raw” colors.
A compass in the right-hand corner of the Image Viewer can be used to rotate the brain by clicking and dragging your cursor. You can zoom using either the wheel on your mouse or using the Zoom scrollbar in the lower right hand corner of the Image Viewer.
A way to control projection visibility is by setting thresholds on projection signal values. This method can restrict visible signals to different combinations such as low intensity and low density or high intensity and low density.
The graph in the lower right hand corner shows a dot for each streamline endpoint, shown as a cube, in a projection experiment. The color of the dot corresponds to the anatomic annotation in the same way the atlas colors display mode works. Each data point is plotted according to its density on the x-axis and its intensity on the y-axis.
The thresholds can be changed by resizing the white box. Any edge or corner of the box can be clicked and dragged to re-size it. You can also click and drag in the center of the box to move the box.
The Structure Ontology Viewer shows the entire collapsible ontology for the mouse brain as defined by the Allen Reference Atlas. Two columns to the right of the ontology determine the type of data displayed in the Image Viewer. “A” represents annotation and when checked, will show a visual representation of that structure in the Image Viewer. “D” represents signal density and when checked, will show signal in that structural domain.
The default organization for the Structure Ontology is the Hierarchical View, but if you are unfamiliar with the ontology, you can click on the Alphabetical View to see the structure list in alphabetical order.
The Bookmarks tab is a space where you can create and save favorite views of the brain. Several default views are already saved that will rotate the brain back into common viewing frames.
This section displays projection experiments you have selected as well as any gene expression experiments you have downloaded in this session. Projection data is indicated by a colored square, gene expression by a colored circle. Right clicking on the gene name or injection site will bring up a menu where you can, 1) view the gene or experiment detail page (Get Info), 2) be taken to a zoomed in image from this experiment (View Images), 3) copy meta information to the clipboard, such as symbol, name, Entrez ID, image-series ID (Copy Info), 4) activate a “Find Correlates” search finding experiments with similar profiles (Find Similar) or 5) close the experiment and remove it from the list and the 3-D view (Close).
To search for genes within the Brain Explorer application: go to the Search box located above the ontology panel and type in the gene symbol or part of a gene name.
The list of results shows gene name, gene symbol along with a 3-D summary thumbnail of the expression for each experiment matching the search. The expression thumbnail represents a maximum expression projection rendering: the denser the expression in a region the more “solid” the appearance. Reference atlas colors are additionally layered on top.
To load an experiment for viewing click on the “Download” button under the gene name.
: Selects cursor rotation tool mode
: Selects cursor pan tool mode
: Selects cursor selection tool mode
: Toggle Sagittal Atlas section viewing
: Toggle Coronal Atlas section viewing
: Toggle Horizontal Atlas section viewing
: Centers the Viewer on the current pinpointed expression data point
: Turns on the cutting planes
: Toggles the Structure Ontology and Gene List View
You can show opaque three dimensional structures of the brain by “showing” or “hiding” structures from this menu. The “Transparent” function allows you to see transparent views of the structures to view the anatomical relationships between them.
Selecting the sagittal, coronal or horizontal sections (or clicking on one of the section image buttons in the toolbar) will superimpose a single plane of the Nissl images from each brain on your image space. These planes can be moved once the selection tool mode button in the toolbar is selected. Selecting “Show Annotation on Section” from this menu will color the Nissl images according to the brain structure ontology.
Select “Show Full Resolution Image” to link to the high resolution annotation reference atlas images.
The Data Tab menu allows to you to show all signal, hide all signal (for instance to then select a single structure) or toggle expression (for instance, unselect your region of interest then toggle to see signal in only that region).
You can also show or remove threshold controls and choose the visual representation of your data from this menu. There are several options under “Raw” colors:
• User defined: each experiment is rendered in user specified color. This mode is useful to distinguish between individual experiments when multiple experiments are being displayed.
• Atlas: In this mode the signal is colored by the corresponding reference atlas structure color. This mode is useful for quickly seeing the annotated regions where a fluorescent signal is detected.
• Signal Level: this mode display average signal intensity and is useful for identifying areas of very high signal.
To be taken to the experiment contact sheet page, select “Get Info”. To see a high resolution view of the images in this experiment choose “View Images”. These functions are also available by right-clicking on the injection site/gene name in the Gene/Projection List.
Choose “Find Similar” to find similar experiments to the selected experiment. This uses the same NeuroBlast functionality as in the web application.
When this function is selected, either by toggling the cutting tools button in the toolbar or selecting “Clipping Planes” from the View drop down menu, you can make coronal, sagittal or horizontal cuts in your view of the brain and related data. To cut in a particular plane, make sure the cursor is in selection tool mode, and then click and drag on the plane you are interested in clipping.
If you are using a desktop computer, you should obtain drivers from the video card manufacturer. First, identify the video card. Go the Start menu and open the Control Panel. Open the Display control panel and go to the Settings tab. Click the Advanced button and go to the Adapter tab. Your video card vendor and model name will be displayed at the top of the window under Adapter Type. Please go to the manufacturer’s web site, locate the driver download, and follow the instructions on the website or included with the downloaded file.
If you are using a laptop computer, you will need to go to your laptop manufacturer’s web site to locate the latest video drivers.
You can also activate an alternate drawing mode in Brain Explorer. Go to the View menu and select Options. Check the Draw faster but at lower quality button and uncheck the Synchronize drawing with the monitor’s vertical refresh button. Set the Multisample setting to Off.
If you are using multiple video cards from different vendors, the 3-D display may not work correctly on all attached monitors.
Use the Add/Remove Programs control panel or the uninstall link in the Brain Explorer folder in the Start menu. Additional data that are not automatically uninstalled are located at the following locations:
Atlas data: C:\Documents and Settings\userid\Local Settings\Application Data\Allen Institute\Brain Explorer 2
User settings: C:\Documents and Settings\userid\Application Data\Allen Institute\Brain Explorer 2
Windows Vista and Windows 7
Atlas data: C:\Users\userid\AppData\Local\Allen Institute\Brain Explorer 2
User settings: C:\Users\userid\AppData\Roaming\Allen Institute\Brain Explorer 2
If you use a proxy server, the Brain Explorer application will use the proxy settings from the Internet Options control panel in the Windows Start menu. Please refer to the Windows documentation for help on proxy settings.
Drag the Brain Explorer 2 icon to the trash. The Brain Explorer application generates the following files, which can also be dragged to the trash.
- ~/Library/Application Support/Brain Explorer 2
If the Brain Explorer application is not running smoothly, first try to free up as much memory as possible by quitting all other open applications. You can also activate an alternate drawing mode. Go to the Brain Explorer 2 menu and select Preferences. Check the Draw faster but at lower quality button and uncheck the Synchronize drawing with the monitor’s vertical refresh button. Set Multisampling to Off.