Long Read Sequencing Services

Long Read Sequencing Services

Long reads are excellent tools for assembling complete genomes, organizing highly repetitive regions of the genome, determining the location of removable genetic elements, and methylation studies. At CD Genomics, we are providing long-read sequencing services, including PacBio Sequel and Oxford Nanopore library preparation and sequencing services.

Benefits of our services:

  • Largest sequencing capacity, including the largest Illumina, PacBio SMRT and ONT Nanopore sequencing capacity worldwide.
  • Decades of experience in genomics services and innovative technology platforms.
  • Exceptionally long read lengths (20 kb or more) and unparalleled consensus accuracy.
  • Flexible sequencing strategies and bioinformatics pipelines.
  • Customized services for your biological problems of interest.
  • Fast turnaround time with the most competitive prices.
24 hours support
Tell Us Your Project

We are dedicated to providing outstanding customer service and being reachable at all times.

Dedicated to providing optimal strategy and high quality long-read sequencing services in a fast and cost-effective manner.

Our service is end-to-end and typically consists of five main components, including experimental consultation and design, library construction and QC, short-read/long-read sequencing, data analysis, and after-sales Q&A.

Talk about your projects

For research purposes only, not intended for personal diagnosis, clinical testing, or health assessment

CD Genomics is a leading global life sciences company dedicated to providing high-quality long-read sequencing services to the research community. We specialize in the application of long-read sequencing technologies, including Oxford Nanopore and PacBio SMRT sequencing.