Created by physicians and clinical geneticists, this app analyzes your DNA and provides a straightforward, actionable DNA report. The report includes personalized guidance for protecting and optimizing your health.
The app analyzes your genetic risk of a wide range of preventable diseases. You'll learn what path your genes are putting you on for diseases such as cancer and heart disease.
Knowing your risk means having the chance to lower it. The app provides you with an actionable report that provides clear solutions for optimizing your health.
Be proactive and use the information obtained from your genes to protect your health.
This app analyzes a wide range of preventable diseases, conditions, and medication reactions including:
cancer, including skin, breast, colon, and other forms of cancer
heart disease and heart attack
harmful medication reactions
optimal medication dosage
preventable causes of sudden death
blood clot disorders
A personalized plan of disease prevention may allow you and your doctor to significantly reduce your risk of a large number of diseases and even prevent many from ever forming.
Analysis of your genes may also allow you and your doctor to understand how your body will react to a wide range of medications so that he or she can prescribe those that are likely to be most effective and least harmful.
Learn your risk for, and ways to personalize your prevention of, dozens of common diseases such as
Discover the most effective medications and the optimal dosing based on your genes, as well as what medications to avoid because they are likely to cause harmful side effects.
Genes play a significant role in determining who you are. They dictate not only your physical appearance and many of your personality traits but also your risk for disease and how your body will respond to certain medications. In addition, your genes determine your risk of passing on diseases to your children.
For most common diseases, such as many forms of cancer, heart disease, autoimmune diseases, diabetes and obesity, genes are just one of the factors that determine your risk. Non-genetic factors, such as your lifestyle (what specific foods and beverages you consume, the amounts and types of exercises you perform), the medications you take, and the medical screening procedures you have (colonoscopies, full body skin exams, etc.) may also contribute to overall disease risk and prevention.
This app analyzes data from almost all DNA tests and genome sequencing services. This includes 23andMe, Ancestry, MyHeritage, FTDNA and Dante Labs as well as our own Ultimate DNA Test and Ultimate Genome Sequencing service.
Our new Education Center provides useful information about the latest advancements and discoveries that may impact your DNA and your health. New articles are added every week based on recently published genetic research.
Once your DNA data is stored in your Sequencing.com account, purchase this DNA report, and then click the app's 'Start' button. You'll receive your report in about 30 minutes.
If your DNA data is not already stored in your account, you can either import your data from a DNA test you've already taken (such as from 23andMe or AncestryDNA) or you can order one of our DNA tests.
|Test Compatibility||Format Compatibility||Variant Compatibility||Reference Genome Compatibility|
|Whole Genome Sequencing||FASTQ and FQ||SNP / SNV
(Single Nucleotide Variants)
|hg38 / GRCh38|
|Exome Sequencing||FASTA and FA||INDEL
(Insertion Deletion Variants)
|hg19 / GRCh37|
|Ultimate DNA Test||BAM||hg18 / GRCh36|
|23andMe||SAM||hg17 / GRCh35|
|Dante Labs||Genome VCF (gVCF and GVCF)|
|Genes for Good||CSV|
|HomeDNA||gz and zip compressed files|
|FTDNA||almost all other genetic data formats|
|New Amsterdam Genomics|
|almost all other genetic tests|
Your data is protected by our Privacy First policy. You own your data. We never share or share your data, including your DNA data, with anyone.
Ultimate DNA Test
Ultimate Genome Sequencing
|Amount of genome tested||1%||100%|
|Technology||Enhanced Genotyping Microarray||Clinical-Grade 30x Genome Sequencing|
Silver Membership to Sequencing.com
(includes your choice of DNA analysis apps & reports)
Silver Membership to Sequencing.com
This app uses Sequencing.com's comprehensive database of genotypes and their related phenotypes. This includes relational data pertaining to phenotypes, algorithms to calculate risk (for multifactorial phenotypes) and carrier status (for monogenic phenotypes) and the ability to generate dynamic genetic reports focusing on straightforward, useful insights.
A multifactorial algorithm is used to assess risk of melanoma, heart disease, osteoarthritis and osteoporosis.
A monogenic algorithm is used to assess all other phenotypes. The results of monogenic analysis are one of the following:
Not a carrier
Carrier but not affected
Good news... the app does everything for you.
All you need to do is either upload or import the file containing your genetic data into your Sequencing.com account. Start the app, select the file and the app will handle do everything else.
23andMe data can be uploaded or imported directly from 23andMe (via the Upload Center) while Ancestry.com, Family Tree DNA and The Genographic Project data can be obtained from those services and then uploaded to your account at Sequencing.com. You don't need to do anything to the file you obtain from these services... just upload the file to your secure account at Sequencing.com and then you can use it to power most apps.
Both whole and exome sequencing data can be provided unaligned (such as in FASTQ or FASTA formats), aligned but without variant calling (such as BAM or SAM formats) or in VCF, CRAM or AVRO formats.
Some more good news... the app does this as well. It utilizes an advanced automated approach to determine sex and reference genome (if the file format is downstream of alignment).
Sequencing.com is the world's largest collection of DNA analysis apps and reports. We have an app for almost everything you can find out from your genes.
Genetic analysis and actionable reports for the practicing healthcare professional. Includes assessment and straightforward information for common, preventable diseases and medication reactions.
Analyzes more than 1,200 rare diseases, syndromes conditions and traits. Determines whether a person is a carrier of, or likely affected by, one or more rare diseases. Useful for comprehensive analysis of genetic data as well as preconception screening (to identify diseases a person may carry and may pass on to their children).
The genetic analysis and statements that appear in this app and report have not been evaluated by the United States Food and Drug Administration. The Sequencing.com website and all software applications (Apps) that use Sequencing.com's website, as well as Sequencing.com's open Application Programming Interface (API), are not intended to diagnose, monitor, treat, cure, prevent nor alleviate any disease.