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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.
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Download your AncestryDNA raw data file and upload it for free genetic analysis reports on health and genealogy.
Account details and stored genetic data are not disclosed, sold, rented or shared. Compliance spans HIPAA, HITECH, the US-EU-UK-Swiss Data Privacy Framework and GA4GH.
Obtains data on SNVs/SNPs (single nucleotide variants) INDELs (insertion and deletion variants) Data is aligned to GRCh37 + rCRS MT and is provided in the following files and…
150 base pair paired end 30× sequencing runs on Illumina and MGI DNBSEQ-T7 systems, with reads aligned to GRCh38 and calling for SNVs, indels, CNVs and SVs.
FASTQ, BAM, CRAM and VCF files up to 100gb move into an account through the Upload Center, with a progress bar and troubleshooting steps for stalled transfers.
At Sequencing, we offer a range of interactive apps and DNA reports that provide valuable insights into your genetic data. Understanding the processing times for these tools is…
Store your raw DNA files such as VCF, BAM and FASTQ free of charge in your Sequencing account, with HIPAA compliant security and full ownership.