We provide a full range of RNA sequencing services to help analyze the gene expression patterns, examine changes in the transcriptome, and detect novel RNA molecules, mutations, and gene fusions, enabling a deeper understanding of RNA biology and disease development. In addition to NGS, we provide a long-read sequencing-based method (iso-seq) for full-length transcript sequencing, avoiding errors that can occur with NGS approaches. rna seq data analysis https://rna.cd-genomics.com/rna-sequencing.html

Assays for Transposase-Accessible Chromatin using sequencing, short for ATAC-Seq, is a next-generation sequencing (NGS)-based method to study the open regions of chromatin on a genome-wide scale. ATAC-Seq has the advantages of easy operation, no crosslinking required, high signal-to-noise ratio, and low requirement for sample amount. Combined the data of ATAC-Seq, RNA-Seq, and epigenomics, the relationship between gene differential expression and regulation can be studied more accurately and comprehensively. atac sequencing https://rna.cd-genomics.com/atac-sequencing.html

Single-cell RNA sequencing (scRNA-seq) is a next-generation sequencing (NGS)-based method to amplify and sequence the whole transcriptome of a single cell. It is becoming a powerful tool and has been applied to research related to stem cell differentiation, embryogenesis, whole tissue analysis, and even tumors. single cell seq https://rna.cd-genomics.com/single-cell-rna-seq.html

We provide a full range of RNA sequencing services to help analyze the gene expression patterns, examine changes in the transcriptome, and detect novel RNA molecules, mutations, and gene fusions, enabling a deeper understanding of RNA biology and disease development. In addition to NGS, we provide a long-read sequencing-based method (iso-seq) for full-length transcript sequencing, avoiding errors that can occur with NGS approaches. rna seq data https://rna.cd-genomics.com/rna-sequencing.html

We provide MicroSEQ® microbial identification service based on sequencing of the 16S rRNA gene and ITS/D2 region of 28S large subunit (LSU) rRNA gene to identify the microbial species. microseq microbial identification system https://www.cd-genomics.com/microbioseq/microseq-microbial-identification.html

Pacbio SMRT sequencing technology can sequence a single molecule DNA in real time without amplification, and generates kilobase-long reads with the potential to complete microbial genome assembly. smrt sequencing disadvantages https://www.cd-genomics.com/microbioseq/pacbio-smrt-sequencing.html

We offer professional microbial epigenomics service to analyze the frequency and distribution of methylated residues in microbial genomes for a full understanding of their functions by using Nanopore sequencing technologies. nanopore dna methylation https://www.cd-genomics.com/microbioseq/nanopore-based-microbial-epigenomics.html

We provide professional SMRT-based transcriptomics analysis service to identify novel transcript isoforms, fusion gene expression and alternative splicing events, and improve genome annotation. smrt transcriptomic sequencing https://www.cd-genomics.com/microbioseq/smrt-based-transcriptomics-analysis.html

CD Genomics is a provider of transcriptome bioinformatic data analysis. We can analyze transcriptome raw data of different sequencing platforms, different samples, and different sequencing depths, maximizing the mining of data information. rna seq analysis https://bioinfo.cd-genomics.com/transcriptomics.html

The concept of genomics (genomics) was first proposed by American geneticist Thomas H. Roderick in 1986. Genomics is a cross-biological subject that implements collective characterization, quantitative study and comparative study of different genomes of all genes in organisms. The structure, function, evolution, location, editing and their effects on organisms of genomes can be studied by bioinformatics. ngs data analysis https://bioinfo.cd-genomics.com/genomics.html