GENOME FULL
Whole Genome Sequencing
Whole Genome Sequencing at extraordinary coverage depth for pathogenic mutation detection in rare diseases.
Human genomic content: 3 billion bp.
- 20,000 Human Genes
- All Exons + Introns
- Intergenic Regions
- SNV – Single Nucleotide Variations
- CNV – Copy Number Variations
- mtDNA
- CREs
- Incidental / Secondary Findings
- Secondary Phenotypes
- Carrier Screening 1st level

Accessories: