Whole Genome Sequencing Rare Disease Bundle | DNA Sequencing

Explore your genetic health with our Rare Disease 30x Sequencing Bundle, offering in-depth analysis for over 10,000 rare conditions.

  • Tests: Rare Diseases – 2 Reports Included (see full description below)
  • 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

Description

Dive into a comprehensive understanding of your health with the ‘Rare Disease 30x Sequencing Bundle.’ This advanced whole genome sequencing package is a rare disease DNA test, uniquely crafted to explore more than 10,000 rare diseases, syndromes, and conditions. With the power of Whole Genome Sequencing, you’ll receive detailed insights into your DNA, covering all 30,000 genes and every chromosome, including mitochondrial and Y chromosomes. This kit includes specialized reports to enlighten you on your genetic risks and traits, empowering you with knowledge to take proactive steps in your health journey. It’s a window to unparalleled insights into your genetic makeup, guiding you towards informed health decisions. The Best Genetic Testing!

Full Access To All Raw Genome Data & Analyzed Data:

  • 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

What’s Included | Rare Disease DNA Test

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

INCLUDES 2 REPORTs | Rare Disease DNA Test

  1. Next-Gen Disease Screen (Including EDS)
  2. Wellness & Longevity Report
NextGen Disease Screen (Report) The world’s most comprehensive DNA analysis designed to detect genetic predispositions to more than 10,000 diseases, syndromes and traits.
Wellness & Longevity (Report) The world’s most comprehensive DNA analysis designed to detect genetic predispositions to more than 10,000 diseases, syndromes and traits.

Additional Details | Whole Genome Sequencing

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.

Reviews

There are no reviews yet.

Be the first to review “Whole Genome Sequencing Rare Disease Bundle | DNA Sequencing”

Your email address will not be published. Required fields are marked *

You may also like…