Why does my digital genome contain less than 100% of my genome data?
Microarray, exome and VCF data cover only part of the roughly 3 billion positions in the human genome. Adding FASTQ, BAM, CRAM or WGS data raises the percentage.
The team of bioinformaticians, Genetic Health Coaches, and writers at Sequencing.
The Sequencing team is made up of physicians, bioinformaticians, Genetic Health Coaches, and health writers who create and review the content published on Sequencing. The team draws on backgrounds in medical genetics, personalized preventive medicine, and genetic health coaching to make sure every article reflects current science and gives readers something they can act on.
This byline is used for articles written collaboratively across the team, or when content does not have a single named author. Every article carries the same standard of review regardless of byline.
Microarray, exome and VCF data cover only part of the roughly 3 billion positions in the human genome. Adding FASTQ, BAM, CRAM or WGS data raises the percentage.
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Several FASTQ, BAM, VCF or third-party files from the same person are merged automatically, with the stronger variant calls kept, into a single digital genome.

We do not sell your DNA data. You own your data. You’re always in full control of your data. You can access, download, and permanently delete your data and results at any time.

Whole genome sequencing results take 2 to 3 weeks with Ultra Rapid, 4 to 6 weeks with Expedited and 7 to 8 weeks with Standard, from lab receipt.

Sequencing's whole genome sequencing service is powered by US-based clinical laboratories that are CLIA-certified and CAP-accredited.