Whole Genome Sequencing Services

Discover Single Nucleotide Polymorphisms (SNPs), Copy Number Variation (CNV), and Structural Variation.  Flexible sample type, including FFPE curls or slides, blood, saliva, etc. Scalable high throughput capability operating in CLIA-lab. Bioinformatic support including QC, Mapping, Markdup, BQSR, Germline Variant Analysis, and more.