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.

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

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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.

Human Genomics

With recent developments in throughput and accuracy, long-read technologies have emerged as powerful tools in human genomics, such as resolving some of the most challenging regions of the human genome, detecting previously unavailable structural variants, and generating the first telomere-to-telomere assemblies of entire chromosomes.

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Whole-Genome Resequencing

Improvements in the accuracy and contiguity of genome assembly will inevitably enhance our understanding of more complex forms of genetic variation, which in turn will improve our understanding of mutation and evolutionary processes.

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Animal and Plant Genomics

The study of complex genomes and transcriptomes not only contributes to a better understanding of plant and animal biology at the molecular level, but also helps to protect crop and livestock health.

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Microbial Genomics

Sequencing entire bacterial, fungal, or other microbial genomes is essential and important for generating accurate reference genomes, identifying microbial species, and conducting other comparative genomic studies.

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Transcriptomics

RNA sequencing (RNA-seq) using long-read sequencing is a powerful tool for understanding the cell or tissue transcriptome. Based on advanced platforms and years of experience in transcriptome analysis, we are committed to providing the best strategy to meet the project needs of our global clients.

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Epigenetics and Methylation Analysis

Using long-read sequencing technologies, researchers can directly detect DNA and RNA methylation modifications, such as 5-methylcytosine (5mC), 5-hydroxymethylcytosine (5hmC), and N6-methyladenine (6mA) in DNA, and N6-methyladenosine modification (m⁶A), 5-methylcytosine modification (m⁵C), and N1-methyladenosine (m¹A) in RNA.

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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.