Promethease is a literature retrieval system that builds a personal DNA report based on connecting a file of DNA genotypes to the scientific findings.
Biomedical researchers, healthcare practitioners, and customers of DNA testing services such as 23andMe and AncestryDNA use Promethease to retrieve information published about their DNA variations.
Learn more about Promethease DNA analysis: upload and analyze your genetic data.
Explore your genome for free.
View, search, and learn about your genetic data from any DNA test.
Works with genotyping microarrays (23andMe, AncestryDNA, MyHeritage and similar test providers), exome sequencing and whole genome sequencing (Dante Labs, Nebula Genomics, Full Genomes and similar sequencing providers).
Promethease analyzes your DNA data. To get started, upload or import your DNA data into your Sequencing account.
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 great DNA tests.
You've already taken a DNA test
You need a DNA test
|Our Universal DNA Compatibility enables this app to work with DNA data from almost any genetic test including 23andMe, Ancestry, MyHeritage, FTDNA, and genome sequencing.||Our clinical-grade 30x Whole Genome Sequencing test obtains data on 100% of your genome.|
|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||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|
Compare to 23andMe, Ancestry, MyHeritage and similar that test less than 0.1% of your genome.
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
The wide selection of DNA analysis apps and reports available in our App Market are able to analyze DNA data from any genetic test. This includes data from 23andMe, AncestryDNA, MyHeritage as well as genome sequencing data in any format (fastq, bam, gvcf or vcf).
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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 for carrier screening as well as preconception screening (to identify diseases a person may carry and may pass on to their children).
Explore your genome for free. View, search and learn about your genetic data from any DNA test including genotyping microarrays (23andMe, AncestryDNA, MyHeritage and similar test providers) and whole genome sequencing (Dante Labs, Nebula Genomics, Full Genomes and similar sequencing providers).
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.