CD Genomics is a trusted CRO specializing in population sequencing and integrated genomics services. With headquarters in New York and operations in North Carolina, and Europe, we serve clients in over 50 countries. Our expertise spans next-generation and long-read sequencing, genotyping, microarray analysis, and bioinformatics. By delivering accurate, scalable, and customized solutions, we empower academic institutions, pharmaceutical companies, and agricultural enterprises to advance discoveries in population genetics, drug development, and precision breeding.
As a trusted CRO, we specialize in population sequencing and integrated multi-omics solutions that support researchers in over 50 countries.
Our expertise covers next-generation sequencing, long-read sequencing, genotyping, epigenomics, and bioinformatics, enabling us to deliver accurate, scalable, and customized data solutions. By combining advanced platforms such as Illumina, Nanopore, PacBio, and spatial transcriptomics with tailored bioinformatics pipelines, we empower academic institutions, pharmaceutical companies, and agricultural enterprises to achieve breakthroughs in population genetics, drug discovery, and precision breeding.
With a strong reputation for high-quality results, responsive customer service, and global reach, CD Genomics is committed to being a long-term partner in advancing genomics research.
At CD Genomics, our mission is to accelerate life science discoveries by making advanced population genome sequencing accessible, reliable, and scalable.
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drive breakthroughs in population genetics, drug discovery, and precision breeding.
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provide global researchers with flexible, cost-effective sequencing solutions.
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contribute to food security, healthcare advancements, and biodiversity conservation.
At CD Genomics, we provide a comprehensive suite of genomics services designed to meet the demands of population-level studies. By integrating multiple sequencing platforms with advanced bioinformatics, we deliver accurate, scalable, and actionable insights that support researchers across academia, pharmaceuticals, and agriculture.
From whole genome and exome sequencing to high-throughput SNP genotyping and reduced-representation methods such as RAD-seq, ddRAD, and GBS, we enable researchers to detect genetic variation, population structure, and evolutionary signals with precision.
Our services extend to pan-genome sequencing, combining core and accessory genome analysis to capture the full genetic diversity within a species. We also specialize in ancient DNA sequencing, reconstructing population history and evolutionary events from degraded or historical samples.
Beyond DNA variation, we provide epigenomic and transcriptomic profiling, including DNA methylation microarrays, RNA modification detection, and spatial transcriptomics. These tools allow researchers to explore gene regulation, expression patterns, and population-level epigenetic diversity.
We support every project with tailored bioinformatics pipelines, cloud-based platforms, and advanced statistical genetics analysis. From variant calling to population stratification and GWAS-ready datasets, our informatics team ensures reliable interpretation and publication-ready results.

Access Illumina, Oxford Nanopore, PacBio, and spatial transcriptomics for flexibility in study design and precision in data generation.

Handle hundreds to thousands of samples with optimized workflows designed for large-cohort sequencing projects.

Comprehensive solutions across DNA, RNA, epigenomics, and metagenomics—enabling multi-dimensional insights from a single provider.

Secure global delivery of sequencing results with encrypted digital transfer and cloud accessibility.

Trusted by global researchers, with work featured in peer-reviewed journals such as G3: Genes, Genomes, Genetics, Diversity, and Ecology and Evolution.
Our clients include academic institutions, pharmaceutical companies, agricultural enterprises, and government agencies. CD Genomics has supported research featured in studies such as:
Trusted feedback from researchers and industry partners who collaborated with CD Genomics on population sequencing projects.
"In 2022, our lab conducted a large-scale population resequencing project on maize breeding lines. CD Genomics delivered high-quality SNP genotyping data that allowed us to identify key markers for stress tolerance. The timely delivery and detailed analysis helped us accelerate our breeding program significantly."
— Lead Scientist, Agricultural Research Institute, USA
"Our team collaborated with CD Genomics for a population-scale exome sequencing study in livestock genetics. Dr. Huyang provided outstanding support throughout the project. He was patient in answering our technical questions and offered expert guidance in interpreting complex variant data. His professionalism and responsiveness made the entire process seamless."
— Principal Investigator, Animal Genomics Center, Germany
"We engaged CD Genomics for a microbial population sequencing project in 2023. Their ability to combine Illumina and Nanopore data, together with customized bioinformatics pipelines, gave us a comprehensive picture of microbial diversity. The results were reliable and ready to use for downstream ecological analysis."
— Senior Researcher, Environmental Genomics Laboratory, Japan
Partner with CD Genomics for accurate, scalable, and trusted genomics solutions. Our experts are here to support your research from design to data delivery.