11/08/2023
Hey everyone! 🧬
A while back, we tackled a special challenge: reverse-engineering 23andMe's DNA variants with proprietary identifiers to enhance GenVue. But every challenge has its moments. We noticed inconsistencies, particularly with vital markers like BRCA and MSH2 Lynch syndrome.
Here's a little insight: 23andMe has used various chips over the years, and this can sometimes lead to data inconsistencies. Given this, we've opted to step back from these specific variants. However, the general DNA data (those with an rs #) from 23andMe is still pretty good.
If you're seeking reliable DNA insights, AncestryDNA is a solid choice. But if you want the deepest of dives? Whole Genome Sequencing is unbeatable.
Thanks for riding along with us on this DNA journey! 😊
P.S.
We've recently made GenVue easier to understand for beginners by adding new variant annotations. Check it out:
Upload raw data from AncestryDNA, 23andMe, or upload a Whole Genome Sequencing (WGS/WES) file in .vcf.gz or .vcf format (1 GB max file size) to learn about conditions, drug/chemical response, rare mutations, and more. If you have multiple VCF files, SNP and Indel files are compatible. No information...
