Cell Ranger ATAC4.0 (latest), printed on 10/22/2020
Goal: To learn how to navigate the Loupe Browser interface, load the ATAC Tutorial dataset.
The following image provides an overview of the key components of the Loupe Browser interface. Each of these components are described in more detail below.
The Mouse Selector has three options from left to right:
|Pan - Move the image up and down, or left and right.|
|Rectangular Selection - Select and label a rectangular image area.|
|Lasso Selection - Select and label an image area with an irregular shape.|
The Toolbox is on the left side of the window. Move your mouse over the toolbox icons to see an explanation of what each tool does. The tools in the toolbox perform the functions listed in the table below.
|Zoom In and Zoom Out
Click on + to Zoom In, click on - to Zoom Out, or use the slide bar to zoom in and out.
Autoscale to fit the screen after zooming in or out.
After changes have been made to a .cloupe file, click Save As, name the file, and select a location for the file.
Open a new .cloupe file
Click on the triangle in the bottom right corner and select Export Screenshot as PNG or Export Screenshot as SVG.
Split View can be used with t-SNE to view clusters displayed in the Mode Panel.
Marker Settings can be used with t-SNE and Feature Plot to scale to the point automatically or by percentage. Uncheck the Auto-scale box to choose a percentage.
To return to the home screen and the Recent Files list, click the 10x Genomics button in the top left corner.
The Data Selector Panel is on the left side of the window at the bottom. Move your mouse over the icons to see an explanation of what each tool does. The tools in the Data Selector Panel perform the functions listed in the table below.
|Hide Bottom Panel|
|Load Fragments File|
The View Selector controls what is displayed in the View Panel. There are four different types of views that can be selected:
Common Components Across all ViewsThe following components in the interface are common across all views and are defined in separate sections:
The workspace is centered around the barcode plot, in which single points representing cell barcodes are shown in a variety of projections. Each point represents a single barcode, the vast majority of which represent a single cell. The default projection is the t-SNE plot created by the Cell Ranger ATAC pipeline. Cell Ranger ATAC generates this plot by identifying the most significant peak vectors using dimensionality reduction techniques, and then processing the lower-dimension matrix through t-SNE to produce a two-dimensional scatter plot. You can also view a projection that plots cut site counts in a peak, near a gene promoter, or within a certain motif on two-dimensional axes.
You can click-and-drag the mouse over the cells to reposition the plot, and use the mouse wheel or track pad to smoothly zoom in and out. You'll see cluster labels as you move your mouse over the plot, which is useful for data that has a high number of precomputed clusters. Cells are colored by the active legend in the sidebar.
There are three modes in Loupe Browser for ATAC data including:
Categories mode - where you can see the different cluster assignments for all the cells.
Accessibility mode - where you can overlay quantitative cut site count information atop the barcode.
Filter mode - where you can create complex boolean filters to find specific cell types.
Switching between modes applies mode-specific coloring to the graph, and changes the sidebar to reveal mode-specific functionality.
Cell Ranger ATAC pipelines compute and produce clusterings from two algorithms: a graph-based clustering algorithm and by either K-Means or K-Medoids clustering. A selector at the top of the Categories sidebar allows you to switch between these clusterings, or other clusterings that you can create yourself within Loupe Browser.
You can hide, show and highlight individual clusters within a category by using the sidebar. To highlight a cluster, click on the cluster name within the legend. To toggle the appearance of a cluster, click on the checkbox next to the cluster name. Finally, you can hide or show all clusters within a category by clicking on the menu with three dots to the right of the category selector.
You can also rename and recolor clusters by right-clicking on a cluster name or color, and selecting the desired option from the pop-up menu.
In Accessibility mode, you see a graphical representation of chromatin accessibility across your dataset. You can view the number of cut sites detected per cell within individual peaks, near the promoter regions of particular genes, or in total across the entire genome, through the Peak Sum feature. Each of these views shows the following:
You can also view Z-scores of transcription factor motif counts per barcode, look at one or more features at a time, load and save lists of features for analyzing across multiple datasets, and look at the density of cut site counts across your data. We will explore Accessibility mode more in-depth when looking for cell types.
In Filter mode, you can compose complex boolean filters to find barcodes that fulfill your criteria. You can create rules based on feature counts or cluster membership and combine these rules using boolean operators. You can then save and load filters and use them across multiple datasets. We will introduce filtering in detail and identify complex cell types.
The panel on the bottom of the workspace does double duty for ATAC data in Loupe Browser. The Feature Table shows information about differentially accessible peaks, transcription factor motifs, or promoter sums between clusters.
The Peak Viewer shows the differential distribution of peaks and cut sites per cluster within the genome. You can use the toolbar at bottom left to toggle between the three panels. When you first load the ATAC dataset, you see the feature table preloaded with the transcription factor motifs that are most significantly different between the clusters in the active category. Selecting the Peak Viewer, by default, shows the first five peaks in the genome, and their distribution within the active set of clusters. The Feature Table is explored in depth in Significant Features, and covers how to hone in on regions of interest on the Peak Viewer page.
Now that you are familiar with the user interface, explore the data.