Whole genome sequencing (WGS) covers all genome ranges, such as coding and non-coding regions, with more average sequencing depths and good coverage for areas with higher GCs. In addition to detecting base mutations in small fragments, structural variation analysis of larger fragments can also be carried out, which has better results on the analysis of genetic variation and pathogenesis between individuals and populations.

Specifications:

• Sequencing Mode: NovaSeq 6000, PE 150
• Delivered data: >=90 G, 30X
• Data Format: fastq, or additional purchase of VCF
• Remarks: 45X/60X in-depth sequencing service can be purchased separately. Please contact our sales representatives for a quotation.