Overview
Are You Related?
It's easy to determine if you are related to another person.
This simple to use online app analyzes DNA from two people and calculates their relatedness.
To get started, upload your raw DNA data from any gene test or order a DNA test today.
The results will determine the likely familial relationship, if any, between two individuals such as:
- Father <> Daughter
- Paternal Grandfather <> Grandson
- Maternal First Aunt <> Niece
- Likely Unrelated
Getting Started
This app analyzes and compares DNA from two people.
If the DNA data is not already stored in your Sequencing.com account, you can either import the data from a DNA test you've already taken or you can order a DNA test.
You've already taken a DNA test |
You need a DNA test |
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|---|---|---|---|
| Upload your DNA data | Order a DNA test | ||
| Our Universal DNA Compatibility enables this report to work with DNA data from almost any genetic test | Our clinical-grade 30x Whole Genome Sequencing test obtains data on 100% of your genome. It is the only test that provides enough genetic data for the Comprehensive version of this report. | ||
| For example, DNA data from any of the following test providers will work with this report: 23andMe, Ancestry, MyHeritage, FamilyTreeDNA, Vitagene, Dante Labs, Nebula Genomics, Veritas, Helix and most other DNA test providers. | DNA tests performed by 23andMe, Ancestry, MyHeritage and similar companies test less than 0.1% of your genome. Their tests provide enough data for the Free Report but do not provide the genetic data required for the Comprehensive Report. |
Free DNA Data Upload
Use the Upload Center to upload and use your DNA test or genome sequencing data.
Powered by our Universal DNA Compatibility technology, this report is compatible with data from most genetic 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 | ||||
| AncestryDNA | CRAM | |||||
| MyHeritage | VCF | |||||
| Dante Labs | Genome VCF (gVCF and GVCF) | |||||
| Nebula Genomics | TXT | |||||
| Genes for Good | CSV | |||||
| Living DNA | TAB | |||||
| HomeDNA | gz and zip compressed files | |||||
| FTDNA | almost all other genetic data formats | |||||
| Silverberry Genomix | ||||||
| Toolbox Genomics | ||||||
| Full Genomes | ||||||
| Color | ||||||
| New Amsterdam Genomics | ||||||
| 24Genetics | ||||||
| Vitagene | ||||||
| Helix | ||||||
| Genos | ||||||
| tellmeGen | ||||||
| GSA | ||||||
| Axiom | ||||||
| almost all other genetic tests |
Disclaimer
The genetic analysis and statements that appear in this app 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, treat, cure, or prevent any disease.
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