Transcriptome Service Portfolio
Explore how our RNA sequencing services help researchers profile RNA and explore their pathways.
CD Genomics offers comprehensive RNA sequencing using Next Generation Sequencing technologies.
Key Features of Our RNA Sequencing Services:
High-Quality Data
≥80% bases with ≥Q30, ensuring superior data quality.
Comprehensive Analysis
From total RNA-Seq to single-cell RNA-Seq, we provide deep insights into transcriptomic profiles.
Customizable Solutions
Tailored to meet the unique needs of your project, from targeted RNA sequencing to full-length transcript analysis using Iso-Seq.
Optimized for Performance & Scalability:
Efficient Data Processing
Our state-of-the-art bioinformatics pipeline offers high-speed, high-sensitivity analysis that supports large-scale studies.
Advanced Tools for Deep Insights
From differential gene expression analysis to alternative splicing, explore RNA dynamics with our robust suite of analytical tools.
Explore RNA Sequencing Service Portfolio
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:
Single-Base Resolution
Detect RNA modifications with high accuracy at a single-nucleotide level.
Wide Coverage
Explore a variety of RNA molecules, including mRNA, lncRNA, tRNA, rRNA, and pri-miRNA.
Fast Turnaround Times
Rigorous quality control ensures quick, reliable results for your research.
Customizable Bioinformatics Analysis
Our expert team provides efficient, tailored analysis to meet your specific research needs.
Optimized for Cutting-Edge Research:
High-Throughput Sequencing
Gain comprehensive insights with high-throughput sequencing methods that deliver extensive data on RNA modifications.
Advanced Analytical Tools
Explore multiple modification types simultaneously with services like m7G+m3C sequencing and m6A profiling for in-depth molecular mapping.
Start Mapping RNA Modifications Today!
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:
Detect Novel ncRNAs
Discover new non-coding RNA species and identify potential biomarkers.
High Data Quality
Achieve superior sequencing quality with ≥80% bases at ≥Q30 and >90% on average.
Comprehensive Analysis
Tailored bioinformatics analysis to suit your specific research needs and ensure accurate results.
Wide Range of ncRNA Profiling
From long RNA and circRNA to small RNA, miRNA, and piRNA, we offer specialized sequencing solutions for each RNA class.
Optimized for Complex RNA Profiling:
Long RNA-Seq
For comprehensive profiling of lncRNAs, circRNAs, and mRNAs to understand gene regulation mechanisms.
Small RNA-Seq
Profiling of miRNAs, siRNAs, piRNAs, and more, with options for UMI-based quantification to reduce PCR bias.
Bacterial Small RNA-Seq
Detect novel bacterial small RNAs to explore microbial gene regulation.
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.
Explore ncRNA Dynamics Now!
Key Features of Our Protein-RNA Interaction Services:
High Coverage & Sensitivity
Detect and profile protein binding sites across the entire transcriptome.
Comprehensive Bioinformatics Analysis
Tailored bioinformatics pipelines that offer data visualization, peak calling, motif search, differential binding analysis, and more.
One-Stop Solution
From sample preparation to library construction, sequencing, and data analysis, we provide a seamless workflow to accelerate your research.
Explore the Power of Protein-RNA Interactions:
Our platform supports the study of both coding and non-coding RNAs (e.g., lncRNAs, miRNAs, snoRNAs), allowing for the exploration of complex gene regulation mechanisms such as RNA-protein recognition, gene expression facilitation, and RNA modification impacts. Whether you're investigating cellular homeostasis, disease mechanisms, or RNA drug design, our services provide the essential data to advance your projects.
Unravel RNA-Protein Interactions!
Key Advantages of Long-Read RNA Sequencing:
Single-Base Resolution
Achieve highly accurate analysis at the individual base level with minimal alignment errors.
Identification of Novel Transcripts
Discover new transcripts and alternative splicing events that were previously challenging to detect.
Structural Variants and Repetitive Regions
Resolve structural variants and complex genomic regions, including repetitive sequences, with precision.
Direct Real-Time Analysis
Benefit from real-time sequencing with Nanopore technology, which offers ultra-long read lengths, allowing you to analyze long RNA fragments in a short sequencing time.
Service Portfolio:
Unlock the complete view of transcriptomes by accurately detecting structural variations and providing more comprehensive genetic data.
Achieve ultra-long read sequencing for novel transcriptomics and enhance existing reference transcriptomes.
Detect RNA modifications across the entire transcriptome with single-base resolution, enabling detailed analysis of epitranscriptomic changes.
Accelerate Your RNA Research with Long-Read Sequencing
Whether you're exploring new diseases, refining reference transcriptomes, or investigating alternative splicing, CD Genomics' Long-Read RNA Sequencing services provide the tools you need to uncover deeper biological insights.
Start Mapping Long-Read RNA Sequencing!
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:
Data Quality Control and Annotation
Ensure the highest data accuracy and integrity with comprehensive QC and detailed annotation.
Differential Expression & Functional Analysis
Discover gene expression patterns, identify differentially expressed genes, and uncover key biological insights.
Alternative Splicing & Regulatory Network Analysis
Gain insights into gene regulation and splicing events, and explore complex RNA-protein interactions.
Epigenomics and RNA Modifications Analysis
Analyze the dynamic epitranscriptome and regulatory modifications at a deep, molecular level.
What We Offer:
Comprehensive Analysis
From abiotic and biotic stress to therapeutic responses, our bioinformatics expertise spans a wide range of biological processes.
Data Security & Confidentiality
We ensure a secure, confidential process for all data exchanges, providing peace of mind throughout your project.
Deliverables
FastQ, BAM, coverage summaries, QC reports, and custom bioinformatics analysis reports are all part of our service to help you make data-driven decisions.
Proven Expertise in RNA Data Analysis:
Whether you're studying cancer transcriptomics, drug development, or agricultural applications, CD Genomics' RNA Bioinformatics services empower you to explore, interpret, and visualize your data with unparalleled clarity.
Let Us Help You Navigate the Complexities of RNA Data
