Whole Genome Sequencing and Analysis
Are you looking for human Whole Genome Sequencing and Analysis?
- The most comprehensive method for analyzing the human genome
- Reliable and sensitive detection of genetic variation
- High quality sequencing
- Cost-effective boosting of your research
- Illumina NovaSeq 6000 System
- TRuseq DNA PCR Library or Truseq DNA Nano Library
- 30X coverage, 2x150bp paired end
- QC and analysis report
- Variant calling:
- SNV (single nucleotide variants)
- Indels (Insertions and deletions)
- CNV (Copy Number variants)
- DG Reports visualization of variants
Do you need any other specification or analysis? Are you interested in other species’ genomes?
Contact us to find out more details.