DNA Enhancement
Expand your DNA coverage up to 30M SNPs, merge multiple files, and maximize compatibility.
Enhance, convert, and unlock the full potential of your genetic information with our professional-grade DNA processing services.
Whether you need to enhance coverage, convert formats, or process sequencing data—we have the tools.
Expand your DNA coverage up to 30M SNPs, merge multiple files, and maximize compatibility.
Transform between VCF, RAW, BCF, PLINK, and other genetic file formats seamlessly.
Process WGS, FASTQ, BAM, and CRAM files from advanced sequencing providers.
Transform limited DNA chip data into comprehensive genomic coverage for deeper ancestry analysis.
Extend your DNA coverage from ~700K to approximately 30 million SNPs using statistical inference with the 1000 Genomes reference panel.
Combine up to 5 DNA files from different providers into a single superkit for improved coverage and accuracy.
Maximize your RAW file compatibility across different platforms and testing providers.
Professional desktop application for analyzing, merging, comparing, and managing your RAW DNA files locally.
Seamlessly convert your genetic data between different file formats for maximum compatibility.
Convert VCF variant call format files to universal RAW DNA format.
Learn moreConvert RAW DNA files to VCF format for bioinformatics tools.
Learn moreConvert binary BCF files to RAW format for ancestry analysis.
Learn moreConvert PLINK BED/BIM/FAM files to RAW DNA format.
Learn moreConvert 23andMe imputed files to standard RAW format.
Learn moreProfessional tools for processing whole genome sequencing, FASTQ, BAM, and CRAM files.
Convert whole genome sequencing files from Nebula Genomics, Dante Labs, and other WGS providers to RAW format for ancestry analysis.
Align your raw FASTQ sequencing reads to the Telomere-to-Telomere (T2T) human reference genome for the most complete genomic analysis.
Convert raw FASTQ sequencing files directly to RAW DNA format for immediate use in ancestry analysis platforms.
Our services support RAW files from all major DNA testing companies.
| Provider | Chip/Version | Format | SNPs | Year | Compatibility | Notes |
|---|---|---|---|---|---|---|
| 23andMe | v5 | RAW | ~730K | 2017 | All services | Current chip |
| 23andMe | v4 | RAW | ~600K | 2013 | All services | Legacy |
| 23andMe | v3 | RAW | ~960K | 2010 | All services | Custom chip |
| AncestryDNA | v2 | RAW | ~710K | 2018 | All services | Current chip |
| AncestryDNA | v1 | RAW | ~680K | 2012 | All services | Legacy |
| MyHeritage | v2 | RAW | ~730K | 2019 | All services | GSA chip |
| MyHeritage | v1 | RAW | ~700K | 2016 | All services | OmniExpress |
| FamilyTreeDNA | Family Finder | RAW | ~700K | 2018 | All services | — |
| LivingDNA | GSA v2 | RAW | ~730K | 2019 | All services | — |
| Nebula Genomics | 30x WGS | FASTQ/VCF | 30M+ | 2019 | After conversion | Requires WGS to RAW conversion |
| Dante Labs | WGS | FASTQ/VCF | 30M+ | 2018 | After conversion | Requires WGS to RAW conversion |
| Gene by Gene | GPS Origins | RAW | ~700K | 2016 | All services | — |
| 24Genetics | Custom | RAW | ~700K | 2018 | All services | — |
| National Geographic | Geno 2.0 | RAW | ~150K | 2012 | Limited | Discontinued |
| WeGene | Custom | RAW | ~700K | 2016 | All services | Asia focus |
| Genera | Custom | RAW | ~650K | 2019 | All services | Brazil |
| TellMeGen | Custom | RAW | ~700K | 2017 | All services | Spain |
| Adntro | Custom | RAW | ~700K | 2020 | All services | Spain |
Upload your DNA file and unlock the full potential of your genetic information with our professional processing services.
Most services complete within 24-48 hours. DNA imputation typically takes around 24 hours, while file conversions are usually faster at 12-24 hours. WGS processing may take 48-72 hours depending on file size.
Yes, all files are processed on EU-hosted servers with encryption. Your data is automatically deleted after 15 days, and you can request deletion at any time. We never share your genetic data with third parties.
We support RAW files from all major providers (23andMe, AncestryDNA, MyHeritage, etc.), VCF, BCF, PLINK (BED/BIM/FAM), BAM, CRAM, and FASTQ formats for different services.
Output files are available for download for 15 days after processing. If you need to reprocess, you'll need to place a new order. We recommend downloading your results promptly.
Imputation is a statistical method that predicts genetic variants not directly measured by your DNA chip. By comparing your tested SNPs against reference populations, we can infer approximately 30 million variants from your original ~700K.
Imputed files work great with GEDmatch, MyTrueAncestry, Illustrative DNA, and our own G25 Studio. Higher SNP density provides more accurate ancestry modeling and ancient DNA comparisons.