Whole Genome & Exome Sequencing Services
Genome Sequencing & Variation for Your Research
Study genome-wide and coding variation for disease, cancer, population and trait research, with variant calling and annotation included in the analysis.
- Complimentary sample pickup: Europe & Middle East
- Live project tracking online
- Tailored, itemized quotation
Every variant, genome-wide or coding
What we offer
We provide whole-genome sequencing and resequencing, whole-exome sequencing (WES), and disease- and cancer-focused genome and exome workflows for research characterization of genetic variation.
For population and trait studies, our portfolio includes population genetics and evolution, genome-wide association studies (GWAS), genetic linkage map construction and bulked segregant analysis (BSA), with SNP, InDel and structural variant analysis as the data permit.
Genome Sequencing & Variation Services
Every service below can be quoted individually or combined in one project.
- 01
Standalone DNA sequencing
Sequencing of suitable DNA libraries or DNA inputs
- 02
Whole-genome sequencing / resequencing
Reference-based genome-wide variation
- 03
Disease-focused genome resequencing
Disease-related genome-wide research
- 04
Cancer whole-genome sequencing
Research characterization of tumor alterations
- 05
Whole-exome sequencing (WES)
Variant discovery in coding regions
- 06
Disease-focused whole-exome sequencing
Research on coding variation in disease
- 07
Cancer whole-exome sequencing
Tumor coding-variant analysis for research
- 08
Population genetics and evolution
Diversity, ancestry and population structure
- 09
Genome-wide association studies (GWAS)
Genotype association with measured traits
- 10
Genetic linkage map construction
Genetic markers and inheritance patterns
- 11
Bulked segregant analysis (BSA)
Trait-associated genomic region discovery
- 12
SNP / InDel / structural variant analysis
Variant calling and annotation as data permit
From Your Samples to Clear Results
An automated, tracked process, from quotation to delivery.
- 1
Request a quote
Tell us about your samples and research goals. You receive an itemized quotation by email with a PDF copy.
- 2
Complimentary pickup
For clients in Europe and the Middle East we arrange complimentary pickup of your samples and their shipment to our team in Hong Kong.
- 3
Analysis
Your samples are processed and analysed according to the accepted quotation.
- 4
Results & reports
Data, QC reports and figures are delivered, and every stage is visible in your account.
Frequently Asked Questions
Whole-genome sequencing (WGS) covers the entire genome, while whole-exome sequencing (WES) focuses on the protein-coding regions. WES is often chosen to discover coding variants; WGS also captures non-coding and structural variation.
No. Our genome sequencing services are for research use, such as disease, cancer, population and trait research.
Yes. We work with researchers in Europe and the Middle East and arrange complimentary sample pickup, with the samples shipped to our team in Hong Kong. Every step is tracked live and visible to you online.
Turnaround depends on the service, the number of samples and the analysis required. Your tailored quotation describes the scope of the work for your project.
Send a quote request describing your samples and research goals. Our team reviews it and emails you an itemized quotation with a PDF copy, which you can accept online.
Yes. After you accept the quotation, you can follow each stage of your order, see updates from our team and download your documents in your account.
Plan your genome sequencing project with us
Send us your samples and goals and receive a tailored quotation. Complimentary sample pickup is available across Europe and the Middle East.