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- 1-631-338-8059
info@cd-genomics.com
info@cd-genomics.com
As a seasoned sequencing company, CD Genomics excels in targeted sequencing technology and enrichment strategies. We offer quick, cost-effective, ultra-sensitive, high-throughput testing solutions. These services empower researchers to identify various pathogens, analyze pathogen mutations, and explore disease mechanisms efficiently.
| Service | Application | Advantages |
|---|---|---|
| HBV/HPV/EBV Capture Sequencing | Virus Mutation Analysis | High-sensitivity detection of viral subtypes and mutations for a deeper understanding of viral evolution. |
| Viral Genome Studies | Captures and sequences specific viral gene regions, enhancing research efficiency and data precision. | |
| Virus Subtype Identification | Supports precise identification of various subtypes, applicable to research on multiple virus types. | |
| Pathogens Capture Sequencing | Pathogen Genome Analysis | Precisely captures and analyzes multiple pathogen genomes, supporting large-scale epidemiological studies. |
| Antibiotic Resistance Gene Research | Efficiently detects resistance-related mutations for an in-depth understanding of pathogen resistance evolution. | |
| Multi-Pathogen Detection | Simultaneously detects multiple pathogens, enhancing the comprehensiveness and efficiency of research. | |
| Intestinal Flora Detection | Gut Microbiome Composition Analysis | High-throughput analysis of microbial species and their distribution in the gut, offering precise data for research. |
| Microbial Diversity Assessment | Conducts thorough assessments of microbiome health through alpha and beta diversity analyses. | |
| Microbial Community Studies | Accurately identifies bacterial species in the gut, supporting in-depth studies of the gut ecosystem. |
Get accurate, efficient, and reliable pathogen sequencing results quickly with CD Genomics. Our expert team guides you through each step of the process.
Fill out a form and tell us more about your study and research goals. Our team will help you design the most suitable sequencing plan.
Prepare and submit your samples according to the guidelines on the specific service page, or contact our team for personalized assistance with sample preparation and submission.
Conduct high-precision sequencing using the Illumina platform. Our team then performs detailed data analysis to ensure the accuracy and reliability of results.
We provide a comprehensive analysis report, including data interpretation, charts, and statistical results. Our technical support is also available to help you understand and utilize the data in the report.
The final report for each service will be customized based on specific circumstances and typically includes the following information:
Identifies pathogens present in the sample, including viruses, bacteria, and fungi.
Provides in-depth analysis of pathogen genomes, revealing mutations, gene variations, and potential resistance traits.
Offers detailed data on the composition of gut microbial communities and analyzes interactions between microbes and potential pathogens.
Evaluates the reliability and quality of the data obtained during the experiment to ensure the accuracy of the report content.
Our flexible and comprehensive testing solutions are designed to accelerate your research with precision and efficiency.
Our capture sequencing technology, combined with high-throughput platforms, allows for the detection of multiple pathogens in a short time frame, significantly reducing experimental costs.
Utilizing high-sensitivity and specificity capture sequencing technologies ensures precise pathogen detection, even in low-abundance samples
In addition to offering standard panels, we provide customized services that can design specific capture probes and sequencing strategies tailored to your research needs
From sample preparation to data analysis, we offer full technical support to help you quickly obtain reliable data results, advancing your research progress.
"We ran a metabolic disease project with their intestinal flora service. The 16S platform was solid, and the data came out super clear. Their Standard Data Analysis saved us a ton of time."
Michael Johnson (Principal Scientist)
"Fast, reliable, and picks up low-abundance pathogens. Great service."
Sarah Williams (Associate Director)
"We used CD Genomics' HPV capture sequencing to look at viral mutations. It picked up multiple subtypes and key changes really clearly—way better than what we'd used before. Super helpful for our HPV work."
Emily Thompson (Postdoctoral Fellow)
"We ran a metabolic disease project with their intestinal flora service. The 16S platform was solid, and the data came out super clear. Their Standard Data Analysis saved us a ton of time."
Michael Johnson (Principal Scientist)
Please submit a detailed description of your project. We will provide you with a customized project plan to meet your research requests. You can also send emails directly to info@cd-genomics.com for inquiries.
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