Whole Genome Sequencing (solo/duo/trio)

Whole Genome Sequencing (WGS) captures the complete set of genetic instructions present in an individual's DNA, enabling detection of millions of single‑nucleotide variants, insertions, deletions, and structural changes. Offered in solo, duo, or trio formats, the test can assess personal risk, identify carrier status for recessive conditions, and inform lifestyle or medical decisions based on genetic predispositions. Results may support conversations with a genetics professional about disease susceptibility, pharmacogenomics, or family planning. The package includes a venous blood draw, high‑throughput sequencing of the entire genome, a comprehensive analytical report, and a follow‑up tele‑consultation to interpret key findings. A £50 phlebotomy charge applies for each collection visit.