FAQs

Who is Nebula Genomics?

What does Nebula Genomics offer consumers?

What does Nebula Genomics offer researchers?

How is Nebula Genomics different from its competitors?

What do I need to do to sequence my genome?

What results will I receive if I sequence my genome?

What is Nebula Explore?

How accurate are the results that I will receive?

How long does it take to receive my sequencing results?

Will you also give me my genomic data?

Can I use the Nebula Platform if I live outside the US?

When will clinical-grade whole genome sequencing become available?

How does billing work for Nebula Explore?

What is the Nebula Library?

What is a genome-wide association study (GWAS)?

What is a “polygenic score”?

How do I interpret a polygenic score?

What is a polygenic score percentile and how do I interpret it?

What do small and large allele effect sizes mean?

What does it mean to have none, many or all of the disease-associated variant alleles discovered in a study present in your genome?