As you learn to use IGB, you'll find it offers many features that make it one of the best tools available for visualization and exploration of genomic data sets.
If you are new to IGB, the following six step Quick Start Guide will help you get started using IGB.
1. Go to bioviz.org/igb and click Downloads.
2. Click the IGB image to download and launch IGB. If your computer has enough memory, we recommend choosing the high memory (2 or 5 GB) option.
When IGB first starts, you'll see the IGB start screen shown below.
Open a data source folder under the Data Sources and Data Sets file tree (red box). Select data sets you would like to view by
When you select the data sets you would like to load, IGB will add new track to the main viewer and list the file in the Data Management table (orange arrows). Initially the track will be empty. This allows you to zoom in to a smaller region of interest before loading data into the memory (see Step 5).
To view data
To view data from local or remote files
When you open a file, IGB adds new track to the main view (as a gray place holder track) and adds the file to the list of active data sets in the Data Management Table.
To load data into the main view, click Load Data.
Note: Many data files (especially BAM files) are huge and contain too much data to display at once. For this reason, IGB does NOT automatically load data from a newly opened file. To view data in a file, zoom (See Step 5) and scroll to a region or gene of interest and click Load Data. IGB indicates regions that have not yet been loaded by displaying a slightly darker background color.
If you have a sequence file (fasta, 2bit, bnib, etc.) that you would like to use as the reference sequence, use the File > Open Reference Sequence... option. After selecting the file, click the Load Data button to load sequence into the Coordinate Axis.
If you're working with large files such as .bam, .sam, .wig, .bedGraph, you should 'zoom in' to a smaller area before loading your data, i.e. select a smaller region of data to load. To zoom in on a region of interest, you can:
You can change track color, how IGB indicates strand, track labels, and much more.
To change track appearance
See also: