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