Whole Genome Sequencing

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.

*Turnaround times are indicative and may be subject to sample type and volume.

Why Choose Our Whole Genome Sequencing Services?

Why Choose Whole Genome Sequencing?

Applications of Whole Genome Sequencing?

Service Workflow: Whole Genome Sequencing

Service Workflow: Whole Genome Sequencing
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