Hypervector
DecodeMyBio
SelfDecode
Genomelink
Whole Genome Sequencing for $299
Family Tree DNA
FDNA Face2Gene RESEARCH
Geni
Genomelink Open Biobank
DecodeMyBio analyzes a raw DNA file you already have from 23andMe or AncestryDNA and returns pharmacogenomic reports without a new test. It covers 19 pharmacogenes and more than 150 drug and gene interactions, with guidance graded on CPIC Level A and B clinical evidence.
Reports include Medication Safety, Psychiatric Medications, Pain and Anesthesia, Nutrition and Methylation, Cannabis and CBD, and Celiac and Gluten screening, each with a Clinician Pocket Summary you can share with a prescriber.
Basic trait insights such as caffeine metabolism, lactose tolerance, and alcohol flush are free with an account. Full reports are one-time purchases. Uploaded data is encrypted and auto-deleted after 30 days.
Hypervector DecodeMyBioDecodeMyBio's answer:
DecodeMyBio focuses specifically on how your genes affect your response to medications, not generic trait reports. It reads a 23andMe or AncestryDNA file you already have, analyzes 19 pharmacogenes and more than 150 drug and gene interactions, and grades the guidance on CPIC Level A and B clinical evidence. Every report includes a Clinician Pocket Summary you can hand to a prescriber, and results are one-time purchases with no subscription.
DecodeMyBio's answer:
Most DNA upload tools lead with ancestry or broad wellness traits. DecodeMyBio is built around prescribing decisions: it tells you how you are likely to respond to specific medications, backed by CPIC clinical guidelines rather than general associations. It works from a file you already have, so there is no new test or wait. Reports are one-time purchases instead of a subscription, they include a summary formatted for a clinician, and uploaded data is encrypted and auto-deleted after 30 days.
DecodeMyBio's answer:
People who already have a 23andMe or AncestryDNA raw file and want to use it for medication decisions. That includes anyone starting a new medication who wants to check genetic compatibility, people dealing with unexplained side effects or medications that are not working, and those who prefer data-driven prescribing over trial and error. It is also useful to share with a prescriber.