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Keyword Search Google Search Searching... search Popular Searches Home RNA Sequencing Services RNA Sequencing Dynamic Transcriptome Analysis QuantSeq 3’ mRNA sequencing Strand-Specific RNA Sequencing (stranded RNA-seq) Transient Transcriptome Sequencing Digital RNA Sequencing (UMI RNA Sequencing) Total RNA-Seq Whole Transcriptome Sequencing De Novo Transcriptome Sequencing Reference-Based Transcriptome Sequencing Targeted RNA–Seq CAGE Sequencing Tag-Seq Single-Cell RNA-Seq Drop-Seq Microwell-Seq Single-Cell Full-Length RNA Sequencing Single-Cell RNA Sequencing for Plant Research Cappable-Seq Service tagRNA-Seq Term-Seq Ultralow Input RNA-Seq Dual RNA Sequencing Spatial Transcriptome Sequencing mRNA-Seq Eukaryotic De Novo mRNA Sequencing Eukaryotic mRNA Sequencing with Reference Nonsense-Mediated mRNA Decay (NMD) Analysis Prokaryotic mRNA Sequencing Exosome RNA Sequencing Exosomal Small RNA Sequencing Exosomal lncRNA Sequencing Exosomal microRNA Sequencing Exosomal circRNA Sequencing Exosomal Long RNA Sequencing Exosomal mRNA Sequencing Metatranscriptomics Service PAS Sequencing Poly(A)-Seq Comparative Transcriptome Analysis Gene Expression Profiling by RNA Sequencing Epitranscriptomics O 8 G-Seq hMeRIP Sequencing m1A Sequencing m7G MeRIP Sequencing acRIP Sequencing 2’-O-Methylation Sequencing Pseudo Sequencing m7G+m3C Sequencing m5C Profiling RNA Bisulfite Sequencing (BS RNA-seq) m5C-RIP Sequencing m5C lncRNA and CircRNA Sequencing m6A Profiling MeRIP Sequencing (m6A-seq) m6Am-Seq RNA Methylation Analysis Non-coding RNA Sequencing (ncRNA-seq) ATAC Sequencing 3C Sequencing (Hi-C Sequencing) tRNA Sequencing tRF&tiRNA Sequencing sdRNA (snoRNA) Sequencing Circular RNA Sequencing (circRNA-seq) Degradome Profiling (Degradome Sequencing) ChIP Sequencing Ribo-Seq (Ribosome Footprinting) Long non-coding RNA Sequencing (lncRNA-seq) Small RNA Sequencing (sRNA-seq) miRNA (microRNA) Sequencing Bacterial Small RNA-Seq piRNA Sequencing UMI Small RNA-seq siRNA Sequencing Long RNA-seq (lncRNA+circRNA+mRNA) Tumor Long RNA-seq Exosomal Long RNA-seq Polysome Profiling (Polysome-seq) RNA Interaction Protein-RNA Interactions CLIP Sequencing RNA Immunoprecipitation Sequencing (RIP-Seq) LncRNA and CircRNA RIP Sequencing Long-Read RNA Sequencing (Iso-seq) PacBio Isoform Sequencing Nanopore Direct RNA Sequencing TAIL lso-seq SMRT Full-Length RNA Sequencing Long-Read Epitranscriptomics Sequencing Nanopore full-length cDNA Sequencing RNA Bioinformatics RNA Microarray ceRNA Microarray Service circRNA Microarray Service LncRNA Microarray Service miRNA Microarray Service piRNA Microarray Service Solutions By Sample Type Biofluid Profiling Biofluid Small RNA-Seq Cell-Free RNA-Seq (cfRNA-seq) Biofluid microRNA Sequencing Circulating Cell-Free miRNA Sequencing Blood RNA Sequencing FFPE RNA-Seq By Therapeutic Areas Inherited Disease Oncology Research By Research & Development Phases Biomarker Discovery Drug Research and Development High-Throughput Gene Expression Screening By Sector Microbiology Microbiota Research Virus Identification Double-Stranded RNA Sequencing (dsRNA-Seq) Food & Agriculture Non-Coding RNA Research Solutions Integrative lncRNA Solutions lncRNA Modification Analysis lncRNA Target Prediction lncRNA-Chromatin Interaction Analysis lncRNA-Protein Interaction Prediction lncRNA-RNA Interaction Prediction Integrative circRNA Solutions circRNA Modification Analysis circRNA-miRNA Interaction Analysis circRNA-Protein Interaction Prediction Integrative microRNA Solutions microRNA Expression Analysis microRNA Target Prediction miRNA-mRNA Interactions Analysis Integrative pri-miRNA Solutions Integrative rRNA Solutions Integrative Small RNA Solutions Integrative tRNA Solutions lncRNA-miRNA-mRNA Interactions Analysis Transcriptional Regulation Transcriptional Start Site (TSS) Analysis Resource CompanyContact Us Careers Inquiry Platforms Sample Guideline Simplify your liquid biopsy research. Exosome RNA Sequencing Powering your exosome data with sequencing solutions to expand biomarker discovery, from exosomal small RNA to lncRNA, as well as cell-free RNAs. Learn More Mining information hidden in RNA. RNA Sequencing Comprehensive coding and non-coding RNA sequencing services based on NGS. Learn More Your trusted partner for RNA modification detection. Epitranscriptomics Solution m7G, m3C, m1A, 5mC, 5hmC, m6A, m6Am, Acetylation, 2’-O-Methylation, and More Learn More Empowering your research on RNA–protein interactions. RIP Sequencing Validate RNA-protein interactions, map extensive RNA-RBP networks, and delve into interactions with ncRNA, lncRNA, and miRNA on a genome-wide scale. Learn More Featured RNA Sequencing Services We are ready to help you detect both known and novel RNA with cutting-edge sequencing technologies, profiling non-coding RNA, biofluid RNA, and many more… Speak to our scientists Epitranscriptomics We provide a full range of epitranscriptomics services to investigate RNA modifications including m7G, m3C, m1A, 5mC, 5hmC, m6A, m6Am, acetylation, and 2’-O-methylation. Non-coding RNA Sequencing We help you study the ins and outs of ncRNA – to examine their changes in the abundance across samples, detect novel non-coding RNA molecules, and reveal the complex networks of interaction with other DNA/RNA/proteins. Biofluid Profiling We can assist you in investigating the levels of RNA molecules in biofluid samples (such as whole blood, serum, plasma, lymph or cerebrospinal fluids, saliva, etc.) using high-throughput sequencing technologies for medical research. tRF&tiRNA Sequencing Ribo-Seq RNA Bisulfite Sequencing Degradome Profiling More Technologies DIVERSE SAMPLE TYPES, ONE EXPERT SOLUTION We embrace the diversity of your research needs. Our commitment to accommodating a wide range of sample types sets us apart as your trusted partner in RNA sequencing. Whole Blood Plasma Serum Urine Exosome Cell-Free DNA/RNA Single Cell Cerebrospinal Fluid (CSF) Cell Ultra Low Input Microbial Sample FFPE Animal Tissue Plant Tissue Our Capacity Research Areas CD Genomics provides technologies and services that meet your research purposes. Oncology Research LEARN MORE Inherited Disease LEARN MORE Drug Research & Development LEARN MORE Microbiology LEARN MORE Our RNA Sequencing Service Workflow Sample Preparation Careful processing of the samples ensures the fidelity of data. Library Construction A variety of adapted high-quality kits for library construction. Sequencing Next-generation sequencing and third generation sequencing platforms. Bioinformatics Analysis Detailed bioinformatics analysis provides high-value data. Presenting the newest vision of the groundbreaking RNA sequencing technologies… How to Identify Gene Promoters and Enhancers by ChIP-Seq Essential techniques and methodologies for uncovering these crucial regulatory elements in the genome. A Beginner’s Guide to RNA Sequencing Ensure you have a clear roadmap to navigate the intricate world of RNA sequencing. Plan Your Next Exosome RNA Sequencing Experiment How to perform next-generation sequencing -based exosome transcriptome analysis and the cutting-edge applications. More Perspectives… VALUED PARTNERSHIPS Our dedication to RNA sequencing excellence has garnered the trust of industry leaders and esteemed research institutions. We cherish these partnerships and are privileged to share in their commitment to advancing science.CD Genomics is an advanced biotech company with years of expertise in high-throughput sequencing technologies and transcriptomics bioinformatics. We offer our global customers integrative and flexible RNA sequencing solutions with greater speed and precision, not merely for mRNA, non-coding RNA, RNA modifications, and RNA interactions. Through years of experience in sample optimization and services management, CD Genomics has successfully collaborated with many pharmaceutical companies and institutions, fueling pathbreaking advancements in both academic and clinical research with disease...