Overview
The Integrative Genomics Viewer (IGV) from the Broad Center allows you to view several types of data files involved in any NGS analysis that employs a reference genome, including how reads from a dataset are mapped, gene annotations, and predicted genetic variants.
Get your data
We are going to look at two mapping results- for samples C1_R1 and C2_R2. Download the corresponding bam files and index files from here onto your computer.
Some useful IGV Features
- SNPS
- Coverage tracks- to see coverage in one sample vs another acorss a certain location.
- All sorts of views for paired end data. These help us find analogous pair mappings, split mappings etc.
Launching IGV
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For the remainder of the tutorial, work on your local machine. NOT TACC! |
There are two ways; Launching IGV in your web browser or by downloading the binaries locally and running IGV from your machine. We are just going to run it from web browser for this demo.
In a Web browser
Navigate a web browser to this page:http://www.broadinstitute.org/software/igv/download. You will need to register your email address to use this option!
Go ahead and click on the "Launch with 2 GB" option. This will download a "Java Web Start" file that you can launch by locating it on your Desktop and double-clicking.
Locally on a Mac or Windows computer
Use this link to download IGV:
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If this is not working, you might need to try the web start.
Load genome track on IGV
From the main window of IGV, click on Genomes > Load Genome from server.... Choose dm3 Because our genome is already on the IGV server, we can do this.
Load mapped reads into IGV
From the main window of IGV, click on File > Load from File.... Choose both your bam files.
After loading the reference genome and loading an alignment file, click on the + button in the upper right until reads appear!
Look at one of the differentially expressed genes on IGV
The top 10 upregulated genes from our cuffdiff results were:
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