If you are looking to choose a personal WGS sequencing provider, we recommend looking at List of Personal Genome Sequencing and Interpretation Services from Harvard University. While our tools are compatible with data from many consumer genotyping companies, some (or sometimes many) SNPs may be missing from panels depending on what company and chip version was used for genotyping. The future is moving towards Whole Genome Sequencing and we recommend using Whole Genome Sequencing files with our tools. While these companies try to choose the most important SNPs, the data is far from a complete representation of variation in the genome. While the popular consumer genomic companies genotype hundreds of thousands of pieces of genetic data (called SNPs) from your DNA, this only represents about 0.02% of the genome. Our new product, GenVue Discovery is currently compatible with AncestryDNA, 23andMe and WGS/WES data as well as low-pass sequencing gVCF files. For whole genome sequencing, we are compatible with data from Dante Labs, Veritas Genetics (no longer selling kits), Nebula Genomics, Gencove, Helix Exome+, Genos, and many others. Our panels are also compatible with data from other consumer genomic companies as long as they are formatted like 23andMe data. The genetic raw data DNA interpretation and analysis services on this site require a 23andMe, AncestryDNA, MyHeritage, FTDNA (Family Tree DNA), Living DNA, HomeDNA, Genes for Good, WeGene (China), 23Mofang (China) raw data file or Whole Genome Sequence or Whole Exome Sequence VCF file. Genetic genie offers third party analysis, interpretation and reports for consumer genomic data as well as professional Whole Genome Sequencing (WGS) and Whole Exome Sequencing (WES) files.
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