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Mikhail Dozmorov edited this page Aug 31, 2015 · 2 revisions

GenomeRunner analyzes one or several SNP sets for enrichment in selected categories of regulatory features.

  1. Have your SNP set(s) as lists of rsIDs, or genomic coordinates in BED format, see Input data format.

  2. Keep the default background selection, or upload your own background SNP set, see Background selection.

  3. Select one or several categories of regulatory features, see Database structure.

Click "Submit job"

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Welcome

[Step 1] Input data format

[Step 2] Background selection

[Step 3] Database structure

[Advanced] User provided data

[Advanced] Statistical tests

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