Quickly and scalably identify clinically-relevant phenotype-associated genes and variants.
WuXi NextCODE is the world’s most powerful genome analytics solution. It enables diagnostic marker identification and carrier searches at speeds and scale impossible on any other platform.
Our platform is built on the only big data architecture built from the ground up for genomics. Our clinical applications enable you to query massive datasets on-the-fly and visualize raw sequence instantly.
No other system in the world is being used to manage, mine and interpret more genomes. Our data architecture was built to finding key connections between sequence variants and phenotypes, , with tools that empower users through fully-customizable queries backed by always-on full-resolution data visualization.
The power of the WuXi NextCODE system lies in the computational efficiency of a big data architecture built for genomes. It enables you to query all your data in the context of constantly updated global reference datasets, using simple and powerful toggle filters for allelic frequencies, variant impact prediction and other criteria, with mode of inheritance modeling and de novo detection. All this along with integrated query languages and the ability to bring in your own query scripts in R, Python and others.
Detect novel variants with allelic frequencies down to 0.01%
always-on, constantly updated global reference datasets
A worldwide ecosystem of partners
We offer a full suite of genomics solutions, starting from patient collection data management, sequencing and secondary analysis. Integrated with our analytics, we offer an unmatched comprehensive solution.
Integrate existing processes and use our ecosystem to collaborate with colleagues and institutions around the world. Leverage full-resolution data without moving big files.
Run our system in the cloud to get elastic scalability, compliance and the best-in-class security (powered by DNAnexus). Pay only for the compute time and storage you need.