Trimming bases and filtering reads

Based on pre-alignment QA/QC, we need to trim low quality bases from the 3' end of reads.

• Click the Unaligned reads data node

• Click Pre-alignment tools in the task menu

• Click Trim bases (Figure 1)

Figure 1. Invoking the Trim bases task

By default, Trim bases removes bases starting at the 3' end and continuing until it finds a base pair call with a Phred score of equal to or greater than 35 (Figure 2).

• Click Finish to run Trim bases with default settings

Figure 2. Configure the Trim bases task

The Trim bases task will generate a new data node, Trimmed reads (Figure 3). We can view the task report for Trim bases by double-clicking either the Trim bases task node or the Trimmed reads data node or choosing Task report from the task menu.

Figure 3. A task and a data node are created from the Trim bases task

• Double-click the Trimmed reads data node to open the task report

The report shows the percentage of trimmed reads and reads removed in a table and two graphs (Figure 4).

Figure 4. Results of the Trim bases task

The results are fairly consistent across samples with ~2% of reads untrimmed, ~86% trimmed, and ~12% removed for each. The average quality score for each sample is increased with higher average quality scores at the 3' ends.

• Click RNA-Seq 5-AZA to return to the Analyses tab

Additional Assistance

If you need additional assistance, please visit our support page to submit a help ticket or find phone numbers for regional support.