Transcriptome Sequencing And Data Analysis Service
CD Genomics offers services on the revolutionizing study of the transcriptome, the RNA sequencing. Whether you are targeting to understand previously undetected changes happening in diseases states and responses to therapeutics, or changes under different environmental conditions, CD Genomics provides highly sensitive and accurate tool for measuring such expressions across the transcriptome. The CD Genomics researches are ready to help you detect both known and novel features without limitation to prior knowledge using different RNA sequencing services, epitranscriptomics services, non-coding sequencing services, biofluid profiling, and many more.
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Leading universities, research institutions, and pharmaceutical companies across the world continue to trust us for over a decade, and we continue to deliver on their trust
CD Genomics' Advanced RNA Sequencing Solutions Trusted by Leading Researchers
CD Genomics offers in-depth, intuitive functionalities and features to help you conduct and scale complex transcriptome sequencing and analysis, enabling you to uncover valuable insights into gene expression.
Committed to Providing High-Quality Results
CD Genomics is not only focused on providing various sequencing methods to cover the broad range of researches but also committed to yield high-quality results with the use of the latest technologies released in the market.
Team of Experienced and Expert Scientists
CD Genomics is composed of experienced and expert scientists who ensures the yield of high quality and accurate results for the researches of our dear customers.
Customer Oriented
CD Genomics listens to its customers, from suggestions and requests to feedbacks upon receiving the results. We truly value our customers providing beyond expected service quality while considering their budget and deadline.
Takes Challenges
CD Genomics is leaned towards upgrades and improvements, thus accepting complicated and challenging samples.
Transcriptome Service Portfolio
Explore how our RNA sequencing services help researchers profile RNA and explore their pathways.
Comprehensive RNA Sequencing Services for Cutting-Edge Research
CD Genomics offers comprehensive RNA sequencing using Next Generation Sequencing technologies.
Key Features of Our RNA Sequencing Services:
Optimized for Performance & Scalability:
Advanced Epitranscriptomics Services for RNA Modification Analysis
CD Genomics also provides several epitranscriptonomic sequencing services such as m6A profiling which involves the most common modification in internal mRNA.
Key Features of Our Epitranscriptomics Services:
Optimized for Cutting-Edge Research:
ncRNA-seq for Comprehensive Transcriptomic Analysis
The Non-coding RNA sequencing services offered by CD Genomics ranges from long to short, as well as circular non-coding RNA sequencing.
Key Features of Our ncRNA Sequencing Services:
Optimized for Complex RNA Profiling:
Unlock the full potential of ncRNA research with CD Genomics, and gain deeper insights into the regulatory roles of ncRNAs in health, disease, and development.
Comprehensive Protein-RNA Interaction Analysis for Molecular Insights
Key Features of Our Protein-RNA Interaction Services:
Explore the Power of Protein-RNA Interactions:
Unlock the Power of Long-Read RNA Sequencing
Key Advantages of Long-Read RNA Sequencing:
Service Portfolio:
Accelerate Your RNA Research with Long-Read Sequencing
Expert Bioinformatics Analysis
At CD Genomics, we not only offer cutting-edge RNA sequencing services, but we also provide comprehensive RNA Bioinformatics analysis to maximize the insights from your genomic, transcriptomic, and epigenomic data.
Key Bioinformatics Services:
What We Offer:
Proven Expertise in RNA Data Analysis:
Sequencing Platform
MiSeq
NextSeq 500
NovaSeq 6000
Hiseq X Ten
Unlock Comprehensive Insights with Our RNA Sequencing Sample Report
Download our RNA sequencing sample report to explore detailed, publication-ready analysis of your RNA data. Our final report, delivered via cloud solution or on a hard drive, includes:
An easy-to-read data summary
A clear description of the project, quality assessments of your samples, and a thorough overview of the data analysis results, complete with publication-grade illustrations.
A fully annotated data analysis file
Ready for publication or to conduct your further analysis, offering deep insights into gene expression, alternative splicing, and more.
A materials and methods section
Preformatted for seamless inclusion in your publication.
Encrypted raw data
Including FASTQ and BAM files, ensuring full transparency and reproducibility.
What Our Customers Say About Us
"CD Genomics has been an invaluable partner for our research. Their RNA-Seq service not only delivered high-quality results that exceeded our expectations but also provided us with detailed insights into the gene expression changes associated with neurodegenerative disease progression. From the very first step, the team was highly professional, offering clear guidance and support throughout the process. The bioinformatics analysis was especially impressive, providing us with in-depth insights that were essential for our study. We also appreciated the quick turnaround time and the dedicated customer support. Thanks to CD Genomics, we were able to accelerate our research and achieve our project goals."
Dr. Johannes Müller
Professor of Molecular Biology, Germany
What Our Customers Say About Us
"We have been working with CD Genomics for several years on projects involving cancer immunotherapy. The team is always responsive and willing to go the extra mile to ensure the success of our projects. The quality of the data and the speed of the service are second to none. We particularly appreciate their customized bioinformatics analysis, which has helped us to draw more meaningful conclusions from our data. CD Genomics is a key partner in our research, and I would highly recommend their services."
Dr. Emily Richards
Senior Research Scientist, Stanford University, USA
Application of Transcriptome Sequencing
We understand the significance of your blood RNA sequencing projects. That's why we ensure your samples are handled with the utmost care, utilizing advanced workflows and cutting-edge sequencing technologies to deliver precise and reliable results. With our tailored bioinformatics analysis, your research data will be actionable, helping you discover new biomarkers, gene variants, and therapeutic targets.
CD Genomics offers biofluid profiling services powered by advanced sequencing technologies. Our biofluid sequencing pipeline includes a global network of platforms, including Illumina, PacBio, and Nanopore, ensuring high-quality, reliable results. We support seamless data integration and analysis, with secure cloud storage across multiple regions, ensuring your data is always protected and easily accessible for further research.
Enhance your research with our FFPE RNA-Seq service
Benefit from a seamless process that includes expert sample preparation, high-throughput sequencing, and customized bioinformatics analysis. Our team is here to guide you at every step, ensuring the integrity of your data and helping you uncover valuable insights from challenging FFPE samples.
Supporting your research in inherited disease genetics
With our optimized RNA sequencing workflows, including mRNA, lncRNA, circRNA, and miRNA sequencing, CD Genomics ensures precise gene expression profiling in diverse sample types. Whether you're researching cystic fibrosis, autism, epilepsy, or other inherited conditions, we provide accurate and reliable results for biomarker discovery, gene identification, and drug research. Our professional team will guide you through every step of the process, delivering insights that drive your research forward.
Our RNA sequencing services, including mRNA, small RNA, lncRNA, and circRNA, offer a complete solution for cancer research. We utilize top-tier platforms like Illumina, PacBio, 10x Genomics, and Nanopore to provide accurate and high-quality sequencing results. Our bioinformatics expertise ensures that you can uncover critical information related to tumor heterogeneity, cancer biomarkers, and therapeutic targets.
Accelerate Your Biomarker Discovery with Advanced RNA Profiling
RNA plays a critical role in storing, processing, and transmitting genetic information. Beyond mRNA, non-coding RNAs (ncRNAs) like miRNAs, lncRNAs, and circRNAs are increasingly recognized as powerful biomarkers due to their stability and functional significance. CD Genomics provides a complete RNA sequencing service using cutting-edge platforms such as Illumina, PacBio, and Nanopore, ensuring precise and comprehensive biomarker discovery. Our bioinformatics support offers in-depth analysis, including gene expression, splicing variation, and ncRNA interactions to push your research forward.
Accelerate Drug Discovery with High-Throughput Gene Expression Screening
CD Genomics offers high-throughput gene expression screening using next-generation sequencing (NGS) platforms to provide fast, cost-effective gene expression data. Whether you are investigating compound mechanisms, drug efficacy, or therapeutic responses, our screening service provides reliable and high-resolution data, allowing you to move your projects forward with greater efficiency and precision.
Unparalleled Precision in TSS Analysis
CD Genomics offers state-of-the-art, capture-based sequencing solutions for comprehensive, genome-wide transcriptional start site (TSS) analysis. Our advanced technology ensures that every TSS is accurately identified, providing you with a deeper understanding of gene regulation and its role in development and disease. Whether you're investigating disease mechanisms, drug discovery, or biomarker identification, we offer expert support and customized solutions to meet your research needs. Rest assured, your data is handled with the utmost security, giving you the confidence to focus on your scientific discoveries.
General Service Workflow
Sample submission
Frequently Asked Questions
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- How is the consistency of biological replicates determined? Methods and formulas for biological replicate statistics
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- Should DEGs be represented by Transcripts or Unigenes?
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- What does transcript-id signify? Why might a gene have multiple transcript-ids?
