Our pan-cancer genomic analysis, done on a sample of blood (liquid biopsy), is used to determine the presence of cancer tumor genes and their specific types of mutation from circulating tumor DNA(ctDNA).
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For expectant women, through Non-invasive Prenatal Testing (NIPT), we can determine the risk that the fetus will be born with certain genetic abnormalities. This testing analyzes small fragments of DNA that are circulating in a pregnant woman's blood.
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Partners in forensics, law enforcement, and public safety can benefit from rapid DNA results in many applications. Our systems are designed to provide faster results and greater efficiency than ever before.
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Massive Genomics is a genome sequencing and information company aiming to solve cases of diseases that have a genetic origin; both inherited and sporadic in conjunction with doctors and other scientists.
We aim to solve cases of diseases that have a genetic origin; both inherited and sporadic in conjunction with doctors and other scientists.
A world free of the pain and suffering associated with genetic diseases like cancer by the use of precision medicine technology and processes
Our pan-cancer and myelod genomic analyses help us determine the presence of cancer tumor genes and their specific types of mutation from blood samples.
Learn MoreWe can determine the risk that the fetus will be born with certain genetic abnormalities. This testing analyzes small fragments of DNA that are circulating in a pregnant woman's blood.
Learn MoreOur scientists conduct tests on adults or children to determine their genetic predisposition to various kinds of kidney and heart diseases
Learn MorePartners in forensics, law enforcement, and public safety can benefit from rapid DNA results in many applications. Our systems are designed to provide faster results and greater efficiency than ever before.
Learn More
Our aim is to solve cases of diseases that have a genetic origin; both inherited and sporadic in conjunction with doctors and other scientists.