...

If your Single cell counts data node has been annotated with a gene/transcript annotation, the task will run without a task configuration dialog. However, if you imported a single cell counts matrix without specifying an a gene/transcript annotation file, you will be prompted to choose the genome assembly and annotation file by the Single cell QA/QC configuration dialog (Figure 1).  

Note, it is still possible to run the task without specifying an annotation file. If you choose not to specify an annotation file, the detection of mitochondrial counts will not be possible.

The Single cell QA/QC task report includes interactive opens in a new data viewer session. Three dot and violin plots showing the value of every cell in the project on two or three quality measures are displayed on the canvas (Figure 2).

There are typically three plots: counts per cell, detected genes features per cell, and the percentage of mitochondrial counts per cell. If your cells do not express any mitochondrial genes or an appropriate annotation file was not specified, the plot for the percentage of mitochondrial counts per cell will be absent. non-informative (Figure 3).

Mitochondrial genes are defined as genes located on a mitochondrial chromosome in the gene annotation file. The mitochondrial chromosome is identified in the gene annotation file by having "M" or "MT" in its chromosome name. If the gene annotation file does not follow this naming convention for the mitochondrial chromosome, Partek Flow will not be able to identify any mitochondrial genes. If your single cell RNA-Seq data was processed in another program and the count matrix was imported into Partek Flow, be sure that the annotation field that matches your feature IDs was chosen during import; Partek Flow will be unable to identify any mitochondrial genes if the gene symbols in the imported single cell data and the chosen gene/feature annotation do not match. 

Counts is Total counts are calculated as the sum of the counts for all features in each cell from the input data node. Detected genes The number of detected features is calculated as the number of features in each cell with greater than zero counts. Percentage The percentage of mitochondrial counts is calculated as the sum of counts for known mitochondrial genes divided by the sum of counts for all features and multiplied by 100. 

Each point on the plots is a cell. All cells from all samples are shown on the plots. The pink violins overlaid violins illustrate the distribution of cell values for the y-axis metric. 

There are two methods for filtering cells. First, cells can be filtered by clicking and dragging to select a range on one of the plots (Figure 3)

 The appearance of a plot can be configured by selecting a plot and adjusting the settings in the Configuration cards on the left (Figure 4). Here are some suggestions, but feel free to explore the other options available:

• Open the Color card and reduce the Opacity using the slider. For data sets with very many cells, it may be helpful to decrease the dot opacity to better visualize the plot density.
• Open the Scale card and change the Y-axis scale to Logarithmic. This can be helpful to view the range of values better.
• Open the Summary card and switch on Box & Whiskers. Inspecting the median, Q1, Q3, upper 90%, and lower 10% quantiles of the distributions can be helpful in deciding appropriate thresholds.

...

Image Removed

...

High-quality cells can be selected using the Selection card on the right, which is pre-loaded with three selection rules, one for each quality metric (Figure 5).

Hovering the mouse over one of the selection rules reveals a histogram showing you the frequency distribution of the respective quality metric. The minimum and maximum thresholds can be adjusted by clicking and dragging the sliders (Figure 6).

Alternatively, the filters thresholds can be set using by typing directly into the text boxes below in each plot selection rule (Figure 5Figure 7). The minimum and maximum of the filter can be set using Counts or Percentiles for the Counts filter and Detected genes filters. For the Mitochondrial counts filter, you can set the minimum and maximum mitochondrial reads percentage.  The number and percentage of cells included in the filter is listed at the bottom of the page and updates as filters are added. 

Adjusting the selection criteria will select and deselect cells in all three plots simultaneously. Depending on your settings, the deselected points will either be dimmed or gray. The filters are additive. Combining multiple filters will include the intersection of the three filters. The number of cells selected is shown in the figure legend of each plot (Figure 8).

It can be helpful to view the range of values for Counts and Detected genes on a log scale. To switch the y-axis of these plots to a log scale, click the checkbox at the top of the page (Figure 6)

To filter the high-quality cells, click the Image Added icon in the Filtering card in the top right, and click Apply filter... (Figure 9).

For data sets with very many cells, it may be helpful to decrease the dot opacity to better visualize the plot density. Dot opacity can be adjusted using the slider at the top of the page (Figure 7).

...

Select the input data node for the filtering task and click Select (Figure 10).

...

Image Removed

...

A new data node, Filtered single cell  Filtered counts, will be generated (Figure 8under the Analyses tab (Figure 11).

The Filter cells task report includes the filter criteria, lists the feature distribution statistics for each sample, and gives a breakdown of how many and what percentage of cells were excluded from each sample by each filter (Figure 9). 

...