Our Services & Resources
Our Core and Custom Genomics Services
By utilizing our leading-edge automation and robotics, we can handle large scale, multi-year studies involving up to thousands of samples to ensure that consistent, reproducible libraries are created throughout the duration of the study. Following library preparation, we utilize a fleet of Illumina sequencers, spearheaded by the NovaSeq 6000, to ensure that your data is delivered in a timely manner.
Clinical Reporting Services
Our ISO 15189-compliant, high-quality sequencing and analysis services available for clinical diagnostics.
From tissue extraction to targeted, whole genome/exome/transcriptome, or customized sequencing, we can help at any stage of your genomics research, even if you are working with low input and/or low quality biospecimens.
Our Bioinformatics team utilizes a variety of automated, semi-automated and customized analysis workflows to deliver analyzed data that meets your project’s scientific needs, and analysis summaries that are easy to understand.
How to work with us
What can I submit, and how?
We accept a variety of materials, such as nucleic acids, blood samples, fresh or frozen tissues, formalin-fixed/paraffin-embedded (FFPE) tissues and fully constructed libraries. For information on sample requirements and instructions on how to submit and track samples, please see manuals in our Resource Library for the services you are interested in.
Terms of Service and Policies
Please view our policy documents to understand how we approach collaborations and for important information on data and sample storage.