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In GREAT version 1.2, the whole genome output data was:

  1. term name
  2. term description
  3. total genes (K)
  4. expected gene hits (n*K/N)
  5. gene hits (k)
  6. term gene coverage (k/K)
  7. hypergeometric p-value
  8. binomial p-value
  9. observed region hits (k)
  10. expected region hits (n*p)
  11. genome fraction (p)
  12. gene hits
  13. region hits
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