WHAT'S INCLUDED

• 2 Ancestry composition reports
• +30 Exclusive admixture reports
• 4 Ancient composition reports
• 2 Deep Ancient composition reports
• 3 Archaic composition reports
• Haplogroups: MTDNA and YDNA *
• +200 Traits reports**
• G25 Coordinates (standard and by chromosome)

* Only the files from 23andme contain enough DNA markers to accurately predict a haplogroup.

** The quantity and accuracy of trait predictions depend on the contents of the uploaded RAW file.

WHAT'S INCLUDED

• Everything in Starter pack
• +100 Health reports
• Imputed/Extended RAW file download (+30 Millions of SNPs)

Note: This service imputes your RAW DNA data file from 700K SNPs to 30 million SNPs. The results will be available within 24 hours after a successful payment is processed. The results are received separately in a new sample, which can be found in your account.

This service imputes a RAW DNA data files with 700K SNPs to 30 million SNPs, providing a more comprehensive and accurate understanding of ancestry and genetic traits. Results are available within 24 hours, with instructions provided via email, and a free Starter Pack. Imputed files are compatible with MyTrueAncestry, Gedmatch, and other platforms.

This service imputes 2 RAW DNA data files with 700K SNPs to 30 million SNPs, providing a more comprehensive and accurate understanding of ancestry and genetic traits. Results are available within 24 hours, with instructions provided via email, and a free Starter Pack. Imputed files are compatible with MyTrueAncestry, Gedmatch, and other platforms.

This service imputes 3 RAW DNA data files with 700K SNPs to 30 million SNPs, providing a more comprehensive and accurate understanding of ancestry and genetic traits. Results are available within 24 hours, with instructions provided via email, and a free Starter Pack. Imputed files are compatible with MyTrueAncestry, Gedmatch, and other platforms.

This service imputes 5 RAW DNA data files with 700K SNPs to 30 million SNPs, providing a more comprehensive and accurate understanding of ancestry and genetic traits. Results are available within 24 hours, with instructions provided via email, and a free Starter Pack. Imputed files are compatible with MyTrueAncestry, Gedmatch, and other platforms.

This service converts CRAM or BAM files from several whole-genome sequencing companies to different formats compatible with various tools like Gedmatch, MyHeritage, FTDNA, and Promethease. You have to provide a link to the CRAM/BAM file. The results are ready within 48 hours after purchase.

The DNA Superkit merges RAW DNA files from any company to create a superkit with increased DNA markers and improved accuracy for ancestry and DNA matching results. The tool provides better health predictions, improved matching in Gedmatch, and deeper insights in MyTrueAncestry. The algorithm works with any RAW format sample uploaded to the website. Includes a Starter Pack report.

The RAW to VCF file conversion service allows easy access and analysis of data on various platforms and tools. The resulting VCF file contains all variants in the original RAW file and is securely delivered. Users can access all relevant information, and the service enables easy conversion for analysis on other platforms.

The VCF to 23andme file conversion service allows easy access and analysis of data on different platforms and tools. The resulting 23andme file has all variants contained in the original VCF file. The service is intended for those who need to convert files for other purposes, while those with BAM or CRAM files from whole-genome sequencing tests should use the WGS to RAW file service.

The RAW to 23andme V5 format conversion service provides a converted file that is accepted by most companies. The result file is a 23andme file containing common SNPs present in the source RAW file and is securely delivered. However, the conversion process is not 100% accurate, and some variants may be missing in the result file as the 23andme V5 format may not contain some of the SNPs present in the source RAW file.

The phasing service allows DNA to be divided into two files, one for the mother and one for the father, for a more detailed view of inherited genetic traits. However, each file only contains 50% of each parent's DNA, and the service requires at least one parent's file. The phasing process is only performed for chromosomes 1-22, and haplogroups cannot be phased. This service provides an opportunity to gain deeper insights into ancestry and genetic makeup.

The phasing service divides DNA into two files for a more detailed view of inherited genetic traits. It doesn't require samples from parents but uses algorithms to phase the genome based on a human dataset. Accuracy is around 90%, and the service focuses on chromosomes 1-22. The DUO/TRIO Phasing service can be used if one parent has already been tested. This service provides enhanced genetic insights into ancestry and genetic makeup.

VCF annotation adds extra information to a VCF file, which stores DNA sequence variations like SNPs and small insertions/deletions. It can provide functional consequence details and associations with diseases/traits. The service converts RAW DNA to VCF files, and securely delivers the result.

VCF annotation adds extra information to a VCF file, which stores DNA sequence variations like SNPs and small insertions/deletions. It can provide functional consequence details and associations with diseases/traits. The result file is securely delivered.

Our on-demand Admixture service allows our customers to build their Admixture calculators without any bioinformatics knowledge in a simple way, in a few steps, and totally online.