Biopharma / Research Service
Whole Genome Sequencing
Whole genome sequencing (WGS) is a high-throughput DNA sequencing method that determines all 3.2 billion nucleotides of an individual genetic code in a single test. It enables the analysis of Single-nucleotide variants (SNVs), insertions and deletions (indels), copy number variations (CNVs) and structural variants (SVs), all of which have the potential to provide valuable insights into health, ancestry, and more.
Service Details: Whole Genome Sequencing
What is included?
DNA Extraction (if applicable)
Initial DNA QC
Library Preparation
Sequencing
Alignment and variant calling
Data Delivery
Technical Specifications
Library Preparation Kit: Illumina TruSeq DNA PCR-Free Library Prep Kit
Sequencing Platform: Illumina NovaSeq 6000
Read Type: Paired-end
Read Length: 150 bp
Sequencing Depth: Total mean coverage of ~30X
(alternative coverage options available upon request)
Deliverables
Initial DNA QC Report (.pdf)
Raw data file (.fastq) (available upon request)
Alignment file (.cram) (BAM file available upon request)
Variant file (.vcf)
Sequencing QC Metrics Report (.pdf)
Turnaround Time
2-3 weeks for a batch of up to 96 samples
Sample Requirements
For detailed information about the sample requirements for our Whole Genome Sequencing service, please consult our sample requirements page.
Why Choose Our Whole Genome Sequencing Services?
Why Choose Whole Genome Sequencing?
Applications of Whole Genome Sequencing?
Service Workflow: Whole Genome Sequencing
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