Comprehensive coverage for various research needs.
Comprehensive analysis of the entire genome. Ideal for discovering rare variants, structural variations, and non-coding mutations.
Focused sequencing of protein-coding regions. Cost-effective solution for identifying disease-causing mutations in coding genes.
Deep sequencing of specific gene sets associated with particular diseases (e.g., Cancer, Cardiology, Neurology).
Tailored analysis workflows for unique research requirements, including RNA-seq, ChIP-seq, and multi-omics integration.