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Original file line number Diff line number Diff line change
Expand Up @@ -187,7 +187,7 @@ In this tutorial we use similar tools as described in the tutorial ["Quality con

{% endunless %}

For more information about how to interpret the plots generated by FastQC and MultiQC, please see [this section]({% link topics/sequence-analysis/tutorials/quality-control/tutorial.md %}#assess-quality-with-fastqc---short--long-reads) in our dedicated Quality Control Tutorial.
For more information about how to interpret the plots generated by FastQC and MultiQC, please see [this section]({% link topics/sequence-analysis/tutorials/quality-control/tutorial.md %}#assess-quality-with-falcofastqc---short--long-reads) in our dedicated Quality Control Tutorial.

> <question-title></question-title>
>
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209 changes: 132 additions & 77 deletions topics/sequence-analysis/tutorials/quality-control/tutorial.md

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4 changes: 2 additions & 2 deletions topics/variant-analysis/tutorials/dunovo/tutorial.md
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Expand Up @@ -141,7 +141,7 @@ We then evaluated the quality of the data by running FastQC on both datasets (fo
{: .hands_on}


This created two datasets in our galaxy history: one for forward reads and one for reverse. We then evaluated the quality of the data by running FastQC on both datasets (forward and reverse). You can read about using {% icon tool %} **FastQC** in the dedicated [quality-control tutorial]({{ site.baseurl }}/topics/sequence-analysis/tutorials/quality-control/tutorial.html#assess-quality-with-fastqc---short--long-reads).
This created two datasets in our galaxy history: one for forward reads and one for reverse. We then evaluated the quality of the data by running FastQC on both datasets (forward and reverse). You can read about using {% icon tool %} **FastQC** in the dedicated [quality-control tutorial]({{ site.baseurl }}/topics/sequence-analysis/tutorials/quality-control/tutorial.html#assess-quality-with-falcofastqc---short--long-reads).

This gave us the following plots:

Expand Down Expand Up @@ -408,5 +408,5 @@ You can use the variant calling workflow to call variants using the SSCS instead

You should now understand duplex sequencing, rare variants, and be able to process the former to find the latter.

### If things don't work...
# If things don't work...
...you need to complain. Use [Galaxy's Help Forum](https://help.galaxyproject.org/) to do this.