> For the complete documentation index, see [llms.txt](https://docs.abi.am/abi-omicss-guide-2021/llms.txt). Markdown versions of documentation pages are available by appending `.md` to page URLs; this page is available as [Markdown](https://docs.abi.am/abi-omicss-guide-2021/week-6/ngs/fastqc.md).

# FastQC

Modern high throughput sequencers can generate tens of millions of sequences in a single run. Before analyzing this sequence to draw biological conclusions you should always perform some simple quality control checks to ensure that the raw data looks good and there are no problems or biases in your data that may affect how you can usefully use it.&#x20;

Most sequencers will generate a QC report as part of their analysis pipeline, but this is usually only focused on identifying problems that were generated by the sequencer itself. FastQC aims to provide a QC report which can spot problems that originate either in the sequencer or in the starting library material.

We are going to use FastQC in the scope of this guide, so make sure to thoroughly review the following content.

### [The FastQC Manual](https://dnacore.missouri.edu/PDF/FastQC_Manual.pdf)

### [FastQC Installation Instructions (txt)](https://www.bioinformatics.babraham.ac.uk/projects/fastqc/INSTALL.txt)

### FastQC Documentation (.pptx below)

{% embed url="<https://drive.google.com/file/d/1QTsKGo9DQLgQ5hIQyShXlS8KXhoiRBvs/view>" %}

### Using FastQC to Check the Quality of Throughput Sequence

{% embed url="<https://www.youtube.com/watch?v=bz93ReOv87Y>" %}

## Congratulations!

If you made it here, then congratulations! You have successfully completed this section. Move to the next portion of the guide with the arrow buttons below.


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