We process raw genome sequencing data derived from Illumina, Oxford Nanopore or PacBio technologies and turn it into a meaningful results for detecting inherited traits, rare/de-novo genetic variants significantly correlating with individual phenotypes. We are fully committed to work with our collaborators and clients throughout the process to ensure that the offered analytical results are interpretable and decision maker to manage personalized health.
Personalized Genetic Compatibility Test offers DNA examination from blood samples of a couple who plan for marriage and uncover whether the couple is at risk of conceiving an ill child in future. We take raw genome sequencing data from family members and provide fully tailored list of somatic mutations and their interactions pertaining to the common recessive hereditary diseases. We are capable to provide easy to understand results on risk of common monogenic recessive diseases with statistical odds in their future offsprings.
Our goal is to provide clients high-quality results derived from state-of-the-art methods by measuring gene/isoform expression at a single-sample level that unveil intrinsic underlying mechanism signatures across different scales of biological data for the same complex disease. No matter the discipline or type of data, we pride ourselves on providing professional results.
We all have somewhere around 1500 types of bacteria in our gut, making up a microorganism community (Microbiome) containing about 100 trillion microbes. Our state-of-the-art Metagenomics technologies will quantify functional relationship between the beneficial and harmful microbiome and their impact on crucial aspects of your health. We also provide a personalized Microbiome Index (MI) score that will help to evaluate personalized microbial imbalance, functional dysregulation and inflammation and antibiotic resistance levels in your gut that may need further medical support.
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