Human whole genome sequencing (hWGS) enables researchers to describe the full genetic composition of individuals and characterize entire human genomes. It allows the identification of genomic variation information, including single-nucleotide polymorphisms (SNPs), insertions and deletions (InDels), structural variations (SVs), and copy number variations (CNVs) in a single and cost-efficient assay.
Specifications:
- Sequencing Mode: NovaSeq 6000/X, PE 150
- Delivered data: >=90 G, 30X
- Data Format: fastq, or additional purchase of VCF