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Now that the data has been imported, we need to make a few changes to the data annotation before analysis. 

Modifying Sample Attributes

Notice that the Sample ID names in column 1 are gray (Figure 1). This indicates that Sample ID is a text factor. Text factors cannot be used as a variable in downstream analysis so we need to change Sample ID to a categorical factor. 

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The samples names in column 1 are now black, indicating that they have been changed to a categorical variable. Next, we will add attributes for grouping the data. 

Adding Sample Attributes

  • From the RNA-seq workflow panel, select Add sample attribute to bring up the Add Sample Attributes dialog (Figure 4)

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The attribute will now appear as a new column in the RNA-seq spreadsheet with the heading Tissue and the groups muscle and not muscle. 

Choosing Sample ID Column

The next available step in the Import panel of the RNA-seq workflow is Choose Sample ID Column. Verifying the correct column is designated the Sample ID becomes particularly important when data from multiple experiments is being combined.  

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Numbered figure captions
SubtitleTextChoosing the correct column as Sample ID
AnchorNameChoose Sample ID Column

Performing QA/QC

The next step is to assess the quality of the data by checking the alignments per read. 

  • Select Alignments per Read from the QA/QC section of the RNA-Seq workflow

A new child spreadsheet will be created named Allignment_Counts (Figure 7).

 

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SubtitleTextAlignment_Counts spreadsheet
AnchorNameAlignment counts spreadsheet

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This spreadsheet shows that all reads mapped to one location or did not align to any location. This is dependent on the options used during import. For other data and alignment options, there might be reads with more than one alignment. Reads that were not aligned are listed here because BAM files contain all aligned and unaligned reads; however, unaligned reads are excluded from downstream analysis.  

 

 

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