We offer competitively priced CLIA/CAP certified Whole Genome Sequencing as well as other services as outlined below.

 

Whole Genome Sequencing

Germline

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

Somatic

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

Whole Exome Sequencing

Germline

The UGC uses standard chemistries to achieve a minimum of 250x median coverage of coding regions by targeting the 20,000 genes.

Somatic

Cancer WES services include tumor-normal and tumor-only sequencing and integration with germline DNA and RNAseq information.

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 applications requested by the research community. We provide bioinformatics services to deliver a FastQ, BAM, and VCF formatted files. Examples of libraries for lane sequencing include projects investigation single cell transcriptome, metagenomics, ChIP-seq, and 16S libraries