Study-Driven Design
We begin with the biological question and align workflow selection with sample type, project scope, and expected downstream interpretation.
Research-focused epigenomics services across DNA methylation, chromatin analysis, RNA modification, and epitranscriptomics.
CD Genomics supports epigenetics research with integrated workflows from study design and sequencing to bioinformatics and interpretation-oriented reporting.
CD Genomics provides research-focused support for scientists working across epigenetics and epigenomics. Our platform is built for projects that need more than standalone data generation, combining workflow planning, sequencing support, epigenomic data analysis, and structured deliverables to help researchers move toward biologically meaningful conclusions.
We support academic, translational, and industry teams investigating DNA methylation changes, chromatin dynamics, RNA-associated regulation, and integrated molecular mechanisms. Across these workflows, our goal is to make complex epigenomics studies more accessible, more organized, and more useful for downstream discovery.
Mission: Support researchers with integrated epigenomics workflows that turn molecular profiling into interpretable biological insight.
Vision: Make advanced epigenetics and epigenomics research more actionable through coordinated experimental and analytical support.
Values: Scientific rigor, transparent communication, and project-oriented collaboration.
Our workflows are designed to reduce fragmentation across experimental execution, sequencing, and bioinformatics support, giving researchers a more structured path from project setup to interpretable results.
We begin with the biological question and align workflow selection with sample type, project scope, and expected downstream interpretation.
Quality checkpoints are incorporated across sample review, experimental processing, sequencing, and analytical steps to support consistency and data traceability.
Our workflows are designed not only to process data, but to help researchers better understand methylation patterns, chromatin features, RNA modification signals, and regulatory relationships in context.
Epigenomics projects often involve project-specific decisions. We support communication throughout the workflow so researchers can move forward with greater clarity at each stage.
Our epigenomics services support a broad range of research questions across core areas of epigenetics research.
Support for genome-wide and targeted studies of DNA methylation, including workflows relevant to methylation profiling, comparative analysis, and methylation-linked biological interpretation.
Support for projects exploring hydroxymethylation patterns and related epigenetic regulation in different biological contexts.
Support for chromatin analysis workflows involving chromatin accessibility, protein-DNA interaction, RNA-associated chromatin regulation, and higher-order chromatin studies aimed at understanding regulatory architecture and functional control.
Support for RNA modification studies involving transcript-level regulation and broader epitranscriptomics questions related to post-transcriptional control.
Support for QC, alignment, feature-level analysis, differential interpretation, annotation, and integrative strategies connecting epigenomic data with transcriptomic or other molecular layers.
Sample Types Supported: We support a wide range of sample types used in epigenetics and epigenomics research. For recommended submission formats, handling notes, and project preparation details, please visit our Sample Guidelines page.
A quantitative view of our research support footprint across publications, institutions, experience, and epigenomics coverage.
Our services have supported projects from researchers across academia, biotechnology, and translational science.
Supporting researchers from leading institutions across diverse biological and translational research programs.
The publications below highlight representative research outputs associated with workflows relevant to DNA methylation, chromatin biology, RNA modification, and broader epigenomics analysis.
Representative comments reflecting how researchers evaluate communication, workflow structure, and interpretation support across project stages.
"From the very start, CD Genomics worked hand-in-hand with us to plan our DNA methylation study. Their tips on experiment design saved us time and prevented unnecessary repeats. It's great to partner with a team that communicates so proactively."
"The whole process—from sending samples to getting results—was super smooth. Every stage had a clear contact, and they adapted quickly when we needed special analyses. Professional yet flexible, just how we like it."
"We were new to whole-genome bisulfite sequencing, but their QC reports and clear annotations made everything way easier to handle."
"Their reports link methylation patterns to real biology, with clear figures. Made our internal discussions a breeze."
"For our chromatin accessibility and protein-DNA binding work, their ATAC-Seq and ChIP-Seq services were key. They checked samples carefully, optimized workflows, and were always ready to chat about data. Their support really sped up our downstream experiments."
Our workflow is designed to connect experimental execution, sequencing, and bioinformatics support in a structured, research-oriented way.
We begin with your research objective, sample type, and preferred analytical direction.
Workflow selection is aligned with the biological question and the type of outputs needed for downstream interpretation.
Sample requirements and project details are reviewed before workflow execution.
Experimental and sequencing steps are carried out within a coordinated workflow designed for research-focused data generation.
Data are processed through quality review and analytical pipelines to generate structured outputs for interpretation.
Researchers receive organized deliverables and can discuss project-specific questions relevant to downstream use.
Outputs are organized to support internal review, follow-up validation planning, and downstream analysis workflows.
Our laboratory environment supports sample preparation, workflow execution, and instrument-based research activities across epigenomics studies.
Researchers choose CD Genomics when they need integrated epigenomics services, project-oriented workflow planning, sequencing plus bioinformatics support, publication-oriented outputs, and clear communication throughout the project cycle.
Support across DNA methylation, chromatin analysis, RNA modification, and epitranscriptomics within a coordinated service structure.
Workflows are designed to connect data generation with structured analysis and interpretation-oriented reporting.
Workflow selection and project setup are aligned with the biological question, sample type, and analytical priorities.
Deliverables are organized to support internal review, downstream validation, and broader research communication.
Tell us your research goal, sample type, and preferred direction, and we can help identify a suitable epigenomics workflow for your study.
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