Poly(A) RNA sequencing (RNA-seq) is a next-generation sequencing-based method to comprehensively analyze RNAs with poly(A) tails such as message RNAs (mRNAs) and long non-coding RNAs (lncRNAs). This technique accurately reveals the level of gene expression in your biological sample under specific conditions and generates a complete picture of the transcriptome for the identification of novel alternative splicing, transcripts, gene fusion events, etc. poly a rna https://rna.cd-genomics.com/polya-rna-seq.html

UMI small RNA sequencing (RNA-seq) is a unique molecular identifier (UMI)-based technology for accurate qualitative and quantitative analysis of multiple small RNAs in cells. PCR amplification bias can be removed by adding UMI into each cDNA segment, achieving accurate and unbiased quantification. UMI small RNA-seq can accurately identify SNP, quantify low-abundance transcripts, and reveal comprehensive transcriptome information. We provide UMI small RNA-seq to help you analyze microRNA (miRNA), small interfering RNA (siRNA), piwi-interacting RNA (piRNA) at one time. umi rna seq https://rna.cd-genomics.com/umi-small-rna-seq.html

We provide professional food microbiological testing uing genomics methods including 16S/18S/ITS sequencing, metagenomics, and whole genome sequencing. food microbiology https://www.cd-genomics.com/microbioseq/food-microbiological-testing.html

We provide comprehensive microbiological testing of sewage sludges based on our high-throughput sequencing technology platforms and expertise in bioinformatics analysis.We provide comprehensive microbiological testing of sewage sludges based on our high-throughput sequencing technology platforms and expertise in bioinformatics analysis. "activated sludge microbiology " https://www.cd-genomics.com/microbioseq/microbial-analysis-of-sewage-sludges.html

Long reads are excellent tools for assembling complete genomes, organizing highly repetitive regions of the genome, determining the location of removable genetic elements, and methylation studies. At CD Genomics, we are providing long-read sequencing services, including PacBio Sequel and Oxford Nanopore library preparation and sequencing services. long-read-sequencing https://longseq.cd-genomics.com/services.html

As a leading genomics company, CD Genomics provides next-generation sequencing and bioinformatics services to pharmaceutical and biotech companies, as well as academic and government agencies around the world, relying on advanced sequencing instruments and rich project experience. pacbio-hifi-sequencing https://longseq.cd-genomics.com/pacbio-smrt-sequencing-technology.html

As one of the leading providers of 16S/18S/ITS amplicon sequencing data analysis, CD Genomics uses bioinformatics to help you detect the diversified environmental microorganisms in one step. Our unique data analysis platform can also meet customers' personalized data analysis needs and provide you with a fast analysis cycle and a high-quality result report. its analysis https://bioinfo.cd-genomics.com/16s-18s-its-amplicon-sequencing.html

As a provider of 10x genomics single cell RNA-Seq data analysis, CD Genomics uses bioinformatics to help you explore the secrets of individuals biologically through cells. Our unique data analysis techniques will meet our customers' personalized data analysis needs. We provide a high-quality data analysis platform, a time-efficient analysis, and a high-quality study report. 10x genomics scrna seq https://bioinfo.cd-genomics.com/10x-genomics-single-cell-rna-seq-analysis.html

CD Genomics is offering high-throughput and cost-efficient lncRNA sequencing service by combining the latest Illumina sequencing instruments and advanced bioinformatics analysis. lncrna sequence https://www.cd-genomics.com/lncRNA.html

CD Genomics has been providing the flexible and affordable whole exome sequencing service for couple of years. We employ Illumina HiSeq sequencing platform to obtain the genetic variations information in a more efficient way. exome sequencing https://www.cd-genomics.com/Whole-Exome-Sequencing.html