Moon allows you to download the following files, by using the drop-down menu next to the sample name on the analysis screen:

  • The annotated list of variants in the shortlist of Moon as .csv file
  • An annotated list of all rare variants (PASS in VCF Filter field and gnomAD allele frequency < 2%) with the indication of why these were filtered out by Moon. This list also indicates which variants could (potentially) cause a carrier status for a recessive disease of which the presentation is of relevance for the reported clinical phenotype.

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