Whole Genome Sequencing


We provide competitively priced, CLIA certified, high quality whole genome data and analysis at a variety of coverages. We employ Illumina's NovaSeq 6000 and MiSeq DX seqencing platforms. 


To comprehensively profile the molecular drivers of cancer, the UGC offers tumor only and tumor-normal analyses. We offer integration of somatic DNA analysis RNA analysis at a variety of coverages.

Whole Exome Sequencing


UGC uses standard chemistries to achieve 200x median coverage of coding regions by targeting the 20,000 genes at a variety of coverages.


Cancer WES services include tumor-normal, tumor-only and WES & RNAseq integration at a variety of coverages.

RNA Sequencing

Our mRNA library preparations use oligo-dT beads to enrich polyadenylated RNA molecules, while preserving strand information.

Lane Sequencing

We offer lane sequencing of investigator-prepared libraries. Our lane sequencing is high quality, flexible and supports the diverse application needs of the research community. We provide lane level FASTQ files as the deliverable. Examples of lane sequencing include single cell sequencing, metagenomics, ChIP-seq and 16S libraries.