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  1. Download and install the Integrative Genome Viewer from the Broad Institute. See  Download.
  2. Select "Human hg18" or "Human hg19" as the reference genome
  3. Get some data: File > Load from Server… > 1000 genomes > Alignments > CEU Trio WGS > select those 3 samples
  4. Navigate to the rightmost exons of the GABBR1 gene
  5. Zoom in until you find some SNPs - they might be in exons or introns; there is also at least one example of a short insertion variant between exons 2 and 3
  6. Load and look at the SNP track: File > Load from server > Annotations > Variants and Repeats > dbSNP

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