IGB display reference genomic sequence in the Coordinates track. IGB supports many interactions and views on genomic sequence, including copying sequence, viewing sequence in the Sequence Viewer, and running BLAST searches. Other features may be available via IGB plug-ins.
IGB does not load genomic sequence until you request it, giving you total control over how much data is loaded and when.
To load genomic sequence
Sequence data will then load from a remote data source or local file, depending on whether you're viewing a genome version supported by an external data source or if you're viewing a genome you loaded using the Load Custom Genome option.
If you are working with a genome that is not supported by the IGBQuickLoad data source, let us know. It is easy to add new genome versions to IGBQuickLoad.org.
Some external sequence data servers will reject requests for residues from a region that is too large. Others will return the data, but only after a very long wait. If you have problems, let us know.
If you have a sequence file in one of the formats that IGB can read (File Formats), you can use that sequence as a reference sequence.
To use your own file as the reference genome sequence
IGB will then open the file and it will appear in the Data Management table.
To load data, click Load Sequence button (NOT Load Data) to view the sequence in the coordinate axis.
If the chromosome names do not follow standard synonym conventions you may need to create a personal synonyms file. See: Personal Synonyms.
If the sequence length contradicts your annotation files, IGB will not be able to display them together. Please contact us if you need help.
If you want to load an additional sequence as a track rather than as a reference sequence (perhaps a substrain or an individual), open it as if it were an ordinary file.
As with any other track, a new empty track will appear labeled with the name of the file you opened. The file name will appear in the Data Management table in the Data Access tab.
At low zoom (many bases are shown) loaded sequence is shown as a gray bar beneath the coordinates axis.
When you are zoomed in, the sequence bases become visible. If sequence has not yet been loaded, '-' (hyphen) characters are shown. If the sequence is loaded, the nucleotide base letters are shown. By default, IGB uses cool colors to represent A and T bases and warmer colors to represent G and C bases.
Change base colors in the Preferences > Other Options tab.
Note that depending on the sequence data server, file, or URL that supplied the sequence data, bases may appear in upper or lower case.
In the first image, you can see a sequence loaded as a track (red arrow). Notice that the refseq has not yet been loaded (blue arrow) so it appears gray with '-' marks; when you are zoomed out, the sequence track shows a gray bar (default color), and the coordinate axis is empty.
After loading the refseq (red arrow), the sequence in the track (yellow arrow) changes to the FG color for that track (cyan in this case) where ever it matches the refseq. In this state, it will only highlight differences/mismatches with a letter and a color change. Zoomed out, the track appears as a solid bar in the FG color for the track. The refseq appears as a gray bar in the coordinate axis.
You can copy a sequence of bases into another application, such as Notepad.
To capture a sequence of bases:
If you have selected an annotation that has introns, the selected residues will only include the exon regions.
If you have selected a negative-strand annotation, the selected residues will be reverse-complemented.
If you want to capture all the residues including the intron regions, select the region by dragging in the Coordinates track