Whole Genome Sequencing (WGS) – Ehlers Danlos Screen + 1 Report | DNA Sequencing

Explore your Ehlers-Danlos Syndrome risks with our comprehensive DNA test, covering 3 billion variants and all 30,000 genes for precise analysis.

  • Tests: Full Genome Sequencing + Ehlers Danlos Screen
  • 3 billion genetic variants
  • All 30,000 genes sequenced
  • All chromosomes fully sequenced including the mitochondrial & Y chromosomes
  • 100% of your genome
  • 30x genome sequencing depth
  • Straightforward health reports
  • Free shipping worldwide
  • At-home DNA collection kit (painless mouth swab)
  • You own your data – We don’t sell your data to anyone

Description

Step into personalized health management with our ‘Ehlers-Danlos Syndrome Screening (WGS) Bundle.’ This exceptional whole genome sequencing package – Ehlers Danlos Test is meticulously designed for comprehensive screening of all genes associated with Ehlers-Danlos Syndrome (EDS). The bundle offers an unprecedented depth of genetic analysis, covering 3 billion genetic variants and all 30,000 genes, including complete sequencing of all chromosomes and mitochondrial DNA.

Full Access To All Raw Genome Data & Analyzed Data:

  • Privacy Forever protection of all of your data
  • Next-Gen Disease Screen
  • Genome Explorer v3
  • 1 Month Premium Genome Plan
  • Full access to all raw genome data and analyzed data

INCLUDED REPORTS | Ehlers Danlos Test

Next-Gen Rare Disease Screen (includes comprehensive EDS) The world’s most comprehensive DNA whole genome sequencing with Comprehensive screening of all genes associated with EDS – Ehlers Danlos Syndrome.

Additional Details | Ehlers Danlos Test

Obtains data on around 3 billion positions within your genome (100% of your genome). Also includes the ability to download your raw genome data files for no additional fee. This includes FASTQ, BAM and VCFs covering all genetic variations: Single Nucleotide Polymorphisms (SNPs), Insertions and Deletions (INDELs), Structural Variations (SVs), Copy Number Variations (CNVs) and Mitochondrial Heteroplasmy (MITO).

Privacy First | Whole Genome Sequencing

  • No Insurance Companies – access by insurance companies is strictly prohibited by company policy
  • Keep Results Anonymous – Your Data is stored securely and HIPPA compliant (medical record grade protection). Ensuring no one ever get’s access to your secure data.
  • Submit Anonymously – A bit paranoid about privacy? That’s ok! So are we! Use this guide to create a completely anonymous account (uses a protonmail encrypted email), so that your data is not tied to your personal information.

What Sets Us Apart From Competitors like 23andMe or AncestryDNA?

DNA tests from 23andMe, AncestryDNA, and most other companies use older technology that produces data on a very small subset of the total genome.

Whole genome sequencing is an entirely different class of technology that tests every letter of your DNA, including all ~30,000 genes and all chromosomes end-to-end.

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