SGD

SGD Help: Genomic Stripe View


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Description

The Genomic Stripe View provides a way to display all the regions in the genome that are similar to a selected sequence. The similarities that are displayed are derived from a set of 256 pre-calculated similarity matrices that compare every yeast chromosome to every yeast chromosome. These matrices are the ones used to create the Pairwise Chromosome Similarity View. To learn more about the way the similarity matrices are calculated, see Similarity Data Generation Details.

Using Genomic Stripe View

  1. The Genomic Stripe View Display:

    The Genomic Stripe View display is a set of sixteen black vertical bars, or stripes, representing the sixteen S. cerevisiae chromosomes. They are labelled at the top of the figure, and the scale (in basepairs) is indicated on the left of the figure. Similarities that are at least 25 or 30 base pairs long (depending on the length of sequence used) are indicated as blue or green dots or lines. A blue line indicates that the similarity is is in the direct orientation (when the sequences are lined up from the left arm of the chromosome) and a green line indicates that the similarity is in the indirect orientation. To conserve space in the display, the vertical scale may be compressed relative to that of the horizontal scale. This makes the patterns slightly distorted, but using the Pairwise Chromosome Similarity View (see below) will show you the uncompressed comparison.

  2. Connecting to the Pairwise Chromosome Similarity View:

    Clicking on any part of an image in the figure will show you the Pairwise Chromosome Similarity View for that part of the sequence comparison matrix. Some of the advantages of displaying the Genome-wide DNA Similarity View are that you can zoom in or out, scroll to see a different section of the comparison, or even change the comparison parameters (when the view is zoomed in to the full extent) using "Custom Re-Scan of Current View."

Accessing Genomic Stripe View

Use Gene/Sequence Resources to select a sequence to display using Genomic Stripe View. Simply input the sequence for which you want to view similarities and select Genomic Stripe View as the display option. Note that Genomic Stripe View requires a minimum of 3,000 and a maximum of 100,000 base pairs for the display. If your input sequence is smaller than that, the program will add enough neighboring sequence to make 3000 base pairs. If you enter more than 100,000 base pairs, the program will truncate your sequence. The resulting display will be a graphical representation of sequences throughout the genome that display similarity to your input sequence.

Links to Other SGD Pages

Go to Gene/Sequence Resources


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