<h3>Compatible with data from almost all DNA tests and genome sequencing services.</h3><p><strong><a href="https://sequencing.com/data/upload">Upload Your DNA Data For Free</a></strong></p><div style="width:270px;display:flex;align-items:center;justify-content:center;"><a href="https://sequencing.com/data/upload" style="color:#fff;">Free DNA Data Upload</a></div><table align="left" border="0" cellpadding="0" cellspacing="5" ><thead><tr><th style="text-align: left;"><big>Test Compatibility</big></th><th style="text-align: left;"> </th><th style="text-align: left;"><big>Format Compatibility</big></th><th style="text-align: left;"> </th><th style="text-align: left;"><big>Variant Compatibility</big></th><th style="text-align: left;"> </th><th style="text-align: left;">Reference Genome Compatibility</th></tr></thead><tbody><tr><td><a href="https://dna.sequencing.com/shop-all-bundles/">Whole Genome Sequencing</a></td><td> </td><td>FASTQ and FQ</td><td> </td><td>SNP / SNV<br /><small>(Single Nucleotide Variants)</small></td><td> </td><td>hg38 / GRCh38</td></tr><tr><td>Exome Sequencing</td><td> </td><td>FASTA and FA</td><td> </td><td> </td><td> </td><td>hg19 / GRCh37</td></tr><tr><td>Ultimate DNA Test</td><td> </td><td>BAM</td><td> </td><td> </td><td> </td><td>hg18 / GRCh36</td></tr><tr><td>23andMe</td><td> </td><td>SAM</td><td> </td><td> </td><td> </td><td>hg17 / GRCh35</td></tr><tr><td>AncestryDNA</td><td> </td><td>CRAM</td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>MyHeritage</td><td> </td><td>VCF</td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Dante Labs</td><td> </td><td>Genome VCF (gVCF and GVCF)</td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Nebula Genomics</td><td> </td><td>TXT</td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Genes for Good</td><td> </td><td>CSV</td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Living DNA</td><td> </td><td>TAB</td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>HomeDNA</td><td> </td><td>gz and zip compressed files</td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>FTDNA</td><td> </td><td>almost all other genetic data formats</td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Silverberry Genomix</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Toolbox Genomics</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Full Genomes</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Color</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>New Amsterdam Genomics</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>24Genetics</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Vitagene</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Helix</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Genos</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>tellmeGen</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>GSA</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Axiom</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>almost all other genetic tests</td></tr></tbody>
</table><p> </p><p> </p>


<p>The genetic analysis and statements that appear in this app and report have not been evaluated by Donald Trump or 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.</p>


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