Five3 Genomics

Get Answers Fast.

Discover clinically actionable mutations within a matter of hours, not weeks, with our suite of rapid sequencing analysis algorithms.

Explore your data.

Simultaneously visualize a single sample's mutations, structural rearrangements, copy number abnormalities, and more, providing for the ﬁrst time an integrated view of a single tumor genome.

Simplify your data.

Our state-of-the-art algorithms use biological pathways to integrate many types of genomic measurements, helping you understand the biological implications of genomic disruptions.

Store your data.

Genomic data is no longer an IT nightmare! Store your data with us in our secure data vault and access it from anywhere in the world.

Tools For Researchers

Our genome processing services will take all the tedious work out of your sequencing projects, giving you more time to interact with the data and generate hypotheses. Coupled with the ﬁrst ever integrated tumor browser, you'll be able to drill deep into your data and discover the underlying alterations that may have led to tumorigenesis.

Tools For Biotech

Each tumor presents a challenge to understand the important changes from a unique and complex set of genomic and epigenetic alterations. Our tools can help you understand the common biomarkers that will ultimately determine treatment success.

Compare each patient's data with a large database of public genomic information to understand what alterations are common or unique and the impact of each alteration.

Tools For Everyone Else

Our comprehensive suite of tools can help you identify critical biomarkers in clinical trial data, interpret your genomic data at many levels of detail, and connect you with an expanding community of researchers with data to help empower your research.