We evaluate raw genome sequencing data sourced from Illumina, Oxford Nanopore, or PacBio technologies and transform it into meaningful results for detecting inherited traits, rare or de-novo genetic variants closely linked to specific phenotypes. We are committed to working alongside our partners and clients throughout the entire process to ensure that the analytical outcomes are clear and empower decision-makers to manage personalized health.
The Personalized Genetic Compatibility Test provides DNA analysis from blood samples of a couple intending to marry, revealing if there is a risk of them having a child with health issues in the future. We obtain raw genome sequencing data from family members and deliver a completely customized list of mutations that affect development and their interactions related to common recessive inherited diseases. We can deliver clear results on the likelihood of common monogenic and polygenic recessive diseases with statistical probabilities for their future offspring.
Our aim extends beyond offering personalized genomics; we also deliver advanced reports on comprehensive genomic gene/isoform expression that reveal fundamental underlying mechanism signatures across various levels of biological complexities, with the commitment to clarify clinical interpretation regarding specific genomic causality linked to an individual patient level visible phenotypic traits.
There are roughly 1500 varieties of bacteria in our intestines, forming a community of microorganisms (Microbiome) that includes about 100 trillion microbes. Our advanced Metagenomics technologies will measure the functional connections between the beneficial and harmful microbiome and their effects on essential aspects of your health. We offer a tailored Microbiome Index (MI) score designed to assess individual microbial imbalances, functional dysregulation, inflammation, and antibiotic resistance levels in your gut that might require additional medical attention.
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