Whole Genome Sequencing
Identify mutations and disease states
From DNA extraction, library prep, to genome sequencing, get the full range of services from one laboratory.
Using optimized protocols and technology, we deliver your results in a fraction of the time.
Gain deeper insights with long-read sequencing that captures full-length genes and repetitive regions missed by short-read technologies.
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.
We offer affordable sequencing for microbial and small genomes under 50 Mb.
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!”
“The results look excellent. It’s been a pleasure working with you.”