Whole Genome Sequencing

Identify mutations and disease states

Accelerate Your Infectious Disease Research

All-inclusive services

From DNA extraction, library prep, to genome sequencing, get the full range of services from one laboratory.

Rapid turnaround

Using optimized protocols and technology, we deliver your results in a fraction of the time.

Long-read sequencing

Gain deeper insights with long-read sequencing that captures full-length genes and repetitive regions missed by short-read technologies.

The Use Cases of Whole Genome Sequencing in Research

Drug development

Cancer research

Infectious diseases

Population genetics

Variant studies

Whole genome sequencing is a cornerstone of today’s modern medical research. It provides comprehensive genetic information, enabling researcher to identify unique genetic markers and understand genetic diversity, which is critical for developing targeted therapies and personalized medicine. This technology helps to identify disease-associated genetic variants, allowing researchers to compare genomes to understand disease susceptibility and aid in the development of novel treatments.

Whole genome sequencing also plays a significant role in cancer research by enabling the comparison of tumor genomes and the study of their evolution, as well as in infectious disease research by providing insights into pathogen genetics. In population genetics, it helps researchers understand the genetic structure of populations, and in variant studies, it allows for the detailed analysis of genetic mutations and their implications for health and disease.

Microbial and small genome sequencing

We offer affordable sequencing for microbial and small genomes under 50 Mb.

Microbes

Bacteria
Bacteriophage
Viruses
Plasmids

Small Genomes

Yeast
Parasites
Fungi
Small prokaryotic, eukaryotic & archaeal genomes

The Benefits of Long-read Sequencing

Long-read sequencing is revolutionizing the field of genomics by providing more comprehensive and accurate genome assemblies compared to traditional short-read sequencing methods. With read lengths exceeding 10,000 base pairs, long-read sequencing can resolve complex genomic regions, repetitive sequences, and structural variations that short reads often miss.

This enhanced capability generates complete, high-quality genome assemblies, facilitates the discovery of novel genes, regulatory elements, and disease-associated variants. Long-read sequencing is particularly valuable for de novo genome assembly, metagenomics, and studying organisms with large, complex genomes.

The Sequencing Center uses long-read sequencing to deliver the highest quality reads to ensure researchers will get the best results in their individual downstream bioinformatics.

Leading Research Institutions Choose Us

Experts in genomics trust our whole genome sequencing services for top-quality genomic data.

“This was the fastest turnaround time ever! From cells to full genome sequence in 5 days! We will definitely work together in the future. Thank you!”

Craig RouskeyPando Nutrition

“The results look excellent. It’s been a pleasure working with you.”

Daniel PrestonGreffex

About Us

The Sequencing Center is a leading online knowledge base dedicated to providing news and resources related to genome sequencing technology and life sciences innovations. We offer insights and analyses of the latest advancements in genomics, sequencing techniques, bioinformatics tools, and their practical uses across the life sciences industries. We work with leading research organizations world-wide in various fields including immunology, oncology, transplantation, inherited diseases, neurodegenerative diseases, and drug discovery and development.