Comprehensive Sequencing Solutions: Whole-Genome Discovery to Targeted Precision
Native sequencing and methylation detection capture genomic features that reflect biological reality and can be directly utilized as powerful and informative biomarkers.
Our solutions range from low-pass whole genome sequencing for cell-free DNA (cfDNA), to targeted assays that provide higher coverage of difficult-to-sequence regions of the genome. We deliver accurate results on short tandem repeats (STRs), copy number variations (CNVs), base modifications like methylation and hydroxymethylation, and more—without PCR biases, bi-sulfite conversions, or batch effects.