Choose Your Tier
G30
Our G30 service is 30X whole genome sequencing. This means each letter of your DNA will be read by the sequencer at least 30 times yielding 99% accuracy. G30 suits you if you want high-quality sequencing data and an in-depth genomics report but you are not interested in autoimmune conditions, HLA Typing, carrier status, or deep cancer gene analysis.
$1280
G40
Our G40 service is 40X whole genome sequencing. This means each letter of your DNA will be read by the sequencer at least 40 times, yielding 99.9% accuracy. G40 suits you if you want higher-quality sequencing data and an in-depth genome report including carrier status and deep cancer gene analysis, but you are not interested in autoimmune conditions or HLA Typing.
$1600
G50
Our G50 service is 50X whole genome sequencing. This means each letter of your DNA will be read by the sequencer at least 50 times, yielding essentially 100% accuracy. G50 suits you if you have autoimmune conditions in the family, are interested in HLA typing, are interested in deep cancer gene analysis, or simply want the highest quality sequencing data possible.
$1880
Each service tier delivers all your genome files and genome report to your door and includes complete privacy, weekly updates from our team, and an 8-week turnaround time from the day we receive your saliva sample.
Report Details
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Alzheimer's APOE Genotype, BRCA1/2 basic check, Sudden Cardiac Death, McArdle Disease, Werner's Syndrome, and more.
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Alcohol Flush Reaction, Deep Sleep, Genetic Weight, Lactose Intolerance, Folate Metabolism, Muscle Composition, Saturated Fat and Weight, and Sleep Movement and more.
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Abacavir, Fluorouracil (Adrucil®), NSAID, Peginterferon alpha (PEG-IFN-alpha) & ribavirin (RBV), Phenytoin, Proton Pump Inhibitor (PPI), Simvastatin, Sulfonylurea & Warfarin, and Thiopurine Methyltransferase.
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Bitter Taste, Earwax Type, Fear of Heights, Sweet Tooth, Worrier or Warrior, and more.
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Alpha Thalassemia, Cystic Fibrosis, Canavan disease, Familial Dysautonomia, Fragile X Syndrome, Hemoglobinopathies, Sickle Cell Anemia, Spinal Muscular Atrophy, Tay-Sachs Disease, and many more.
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FH, CHEK2, BARD1, ATM, BRIP1, FLCN, CDH1, CDKNZA, KIT, RET, SDHC, SMARCA4, MSH2, MUTYH, BMPRIA, STK11, PDGFRA, POLE, MSH6, MITF, SDHA, APC, EPCAM, BAP1, CDK4, TSC1, BRCA1, RAD51D, AXINZ, VHL, SMAD4, PALB2, PMS2, RAD51C, SDHD, TMEM127, MET, MSH3, PTEN, PTCH1, TSC2, CDC73, WT1, MENT, RB1, AIP, MAX, NF1, EGFR, GREM1, MLH1, SDHAF2, BRCA2, PRKARIA, TP53, SMARCB1, NTHL1, SDHB, DICERT, LZTRI, HOXB13, POT1, POLD1, NF2, CDKN1B
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High-resolution (second field) reporting of HLA Type. This level of resolution identifies the unique protein sequence of HLA class one and HLA class two genes.
What Customers Say
96% say the service is life-changing.
94% say the service is a great investment.
Gunnar
“I like that I can get my genome without sharing it with the world. As far as I know, this is the only service that allows me to do this. The initial analysis of the genome is very useful.”
William
“It was worth the money. And, indeed, you will never need to be sequenced again. I learned important things about myself from the report and changed a few habits based on those. Overall very happy with the service. ”
Rachel
“They deliver all your DNA data, which is really valuable. Their technical team also helped me look at my variants in the app IGV. Fantastic quality DNA service, lovely staff, and data to last! ”