Next, we will filter out certain cells and re-split the data. Re-splitting the data can be useful if you want to perform differential analysis and downstream analysis separately for proteins and genes. For your own analyses, re-splitting the data is optional. You could just as well continue with differential analysis with the merged data if you prefer.
Because we have classified our cells, we can now filter based on those classifications. This can be used to focus on a single cell type for re-clustering and sub-classification or to exclude cells that are not of interest for downstream analysis.
Click the Merged counts data node
Click Filtering
Click Filter cells
Set to exclude Cell type is Doublets using the drop-down menus
Click OR
Set the second filter to exclude Cell type is N/A using the drop-down menus
Click Finish to apply the filter (Figure 1)
This produces a Filtered counts data node (Figure 2).
Click the Filtered counts data node
Click Pre-analysis tools
Click Split by feature type
This will produce two data nodes, one for each data type (Figure 3). The split data nodes will both retain cell classification information.
Once we have classified our cells, we can use this information to perform comparisons between cell types or between experimental groups for a cell type. In this project, we only have a single sample, so we will compare cell types.
Click the Antibody Capture data node
Click Statistics
Click Differential analysis
Click ANOVA then click Next
The first step is to choose which attributes we want to consider in the statistical test.
Click Cell type
Click Add factor
Click Next
Next, we will set up the comparison we want to make. Here, we will compare the Activated and Mature B cells.
Drag Activated B cells in the top panel
Drag Mature B cells in the bottom panel
Click Add comparison
The comparison should appear in the table as Activated B cells vs. Mature B cells.
Click Finish to run the statistical test (Figure 4)
The ANOVA task produces an ANOVA data node.
Double-click the ANOVA data node to open the task report
The report lists each feature tested, giving p-value, false discovery rate adjusted p-value (FDR step up), and fold change values for each comparison (Figure 5).
In addition to the listed information, we can access dot and violin plots for each gene or protein from this table.
This opens a dot plot in a new data viewer session, showing CD45A expression for cells in each of the classifications (Figure 6). First, we exclude Doublets and N/A cells from the plot:
Open Select and filter, select Criteria
Drag "Cell type" from the legend title to the Add criteria box
Uncheck Doublets and N/A
Click to include selected points
We can use the Configuration panel on the left to edit this plot.
Open the Style icon
Switch on Violins under Summary
Switch on Overlay under Summary
Switch on Colored under Summary
Select the Graph-based clustering node in the Color by section
Color by Graph-based clusters under Color and use the slider to decrease the Opacity
Open the Axes icon
Select the Graph-based clustering node in the X axis section
Change the X axis data to Graph-based clusters
Use the slider to increase the Jitter on the X axis (Figure 7)
Click the project name to return to the Analyses tab
To visualize all of the proteins at the same time, we can make a hierarchical clustering heat map.
Click the ANOVA data node
Click Exploratory analysis in the toolbox
Click Hierarchical clustering/heatmap
In the Cell order section, choose Graph-based clusters from the Assign order drop-down list
Click Finish to run with the other default settings
Double-click the Hierarchical clustering task node to open the heatmap
The heatmap can easily be customized using the tools on the left.
Open the Axes icon
Switch off Show Row labels
Increase the Font to 16 (Figure 8)
Activate the Transpose switch which will switch the Row and Column labels, so now the Row labels will be shown (Figure 9)
Open the Dendrograms icon
Choose Row color By cluster and change Row clusters to 4
Change Row dendrogram size to 80 (Figure 10)
In the Heatmap icon
Navigate to Range under Color
Set the Min and Max to -1.2 and 1.2, respectively
Change the Shape to Circle (Figure 11)
Switch the Shape back to Rectangle
Change the Color Palette by clicking on the color squares and selecting colors from the rainbow. Click outside of the selection box to exit this selection. The color options can be dragged alone the Palette to highlight value differences (Figure 12).
Feel free to explore the other tool options on the left to customize the plot further.
We can use a similar approach to analyze the gene expression data.
Click the project name to return to the Analyses tab
Click the Gene Expression data node
Click the Antibody Capture data node
Click Statistics
Click Differential analysis
Click ANOVA then click Next
Click Cell type
Click Add factor
Click Next
Drag Activated B cells in the top panel
Drag Mature B cells in the bottom panel
Click Add comparison
The comparison should appear in the table as Activated B cells vs. Mature B cells.
Click Finish to run the statistical test
As before, this will generate an ANOVA task node and n ANOVA data node.
Double-click the ANOVA task node to open the task report (Figure 13)
Because more than 20,000 genes have been analyzed, it is useful to use a volcano plot to get an idea about the overall changes.
The Volcano plot opens in a new data viewer session, in a new tab in the web browser. It shows each gene as a point with cutoff lines set for P-value (y-axis) and fold-change (x-axis). By default, the P-value cutoff is set to 0.05 and the fold-change cutoff is set at |2| (Figure 14).
Click the ANOVA report tab in your web browser to return to the full report
We can filter the full set of genes to include only the significantly different genes using the filter panel on the left.
Click FDR step up
Type 0.05 for the cutoff and press Enter on your keyboard
Click Fold change
Set to From -2 to 2 and press Enter on your keyboard
The number at the top of the filter will update to show the number of included genes (Figure 15).
A task, Differential analysis filter, will run and generate a new Filtered Feature list data node. We can get a better idea about the biology underlying these gene expression changes using gene set or pathway enrichment. Note, you need to have the Pathway toolkit enabled to perform the next steps.
Click the Filtered feature list data node
Click Biological interpretation in the toolbox
Click Pathway enrichment
Make sure that Homo sapiens is selected in the Species drop-down menu
Click Finish to run
Double-click the Pathway enrichment task node to open the task report
The pathway enrichment results list KEGG pathways, giving an enrichment score and p-value for each (Figure 16).
To get a better idea about the changes in each enriched pathway, we can view an interactive KEGG pathway map.
Click path:hsa05202 in the Transcriptional misregulation in cancer row
The KEGG pathway map shows up-regulated genes from the input list in red and down-regulated genes from the input list in green (Figure 17).
If you need additional assistance, please visit our support page to submit a help ticket or find phone numbers for regional support.
Click in the CD45RA_TotalSeqB row
Click in the top right corner of the table to open a volcano plot
The plot can be configured using various tools on the left. For example, the Style icon can be used to change the appearance of the points. The X and Y-axes can be changed in the Axes icon. The Statistics icon can be used to set different Fold-change and P-value thresholds for coloring up/down-regulated genes. The in plot controls can be used to transpose the volcano plot (Figure 14).
Click to create a new data node including only these significantly different genes
