ribosome sequencing

CD genomics provides a ribosome-profiling strategy that is based on the deep sequencing of ribosome-protected mRNA fragments and enables genome-wide investigation of translation with sub cordon resolution. Using nuclease digestion, the ribosome position and the translated message can be precisely determined by analyzing the protected ~30-nt area of the mRNA template. ribosome sequencing https://w ww.cd-genomics.co m/ribosome-profiling.html

CD Genomics provides the accurate and cost-effective shallow whole genome sequencing service using Illumina or BGI DNBseq platforms to achieve genome-wide genetic variation for plants, animals and humans. low pass whole genome sequencing https://ww w.cd-genomics.co m/shallow-whole-genome-sequencing.html

Whole-genome resequencing focuses on the analysis of single nucleotide variants (SNV) and small fragment insertion-deletion mutations (InDel), the detection of variants in some repetitive sequence regions, and the detection of structural variants (SV) in large segments. dna resequencing http s://longseq.cd-genomics.co m/whole-genome-resequencing.html

Oxford Nanopore Sequencing Technology (ONT) enables real-time sequencing of native strands of interest without optics or amplification, and its data has been shown to efficiently and cost-effectively improve de novo genome assemblies, structural genomic variants, and more. nanopore sequencing data analysis http s://longseq.cd-genomics.co m/oxford-nanopore-sequencing-data-analysis.html

The viral whole genome sequencing platform at CD Genomics enables us to generate reference-quality viral/phage genomes, for structural genomics and comparative genomics. viral genome sequencing https://ww w.cd-genomics.co m/microbioseq/viral-phage-genome-sequencing-platform.html

Metatranscriptomics elucidates three aspects of a microbial community, including gene activity diversity, gene expression abundance, and differential gene expression analysis. microbial transcriptomics https://w ww.cd-genomics.co m/microbioseq/metatranscriptomics.html

ChIP-Seq, short for Chromatin immunoprecipitation sequencing, is a next-generation based sequencing method to comprehensively study the interaction between proteins and DNA. It takes advantage of the specificity of the antigenic antibody response to provide a fidelity reflection of the binding of protein factors to genomic DNA in vivo. chip seq data analysis htt ps://rna.cd-genomics.co m/chip-sequencing.html

CD Genomics provides a battery of biofluid profiling services utilizing next-generation sequencing technology. Our services can complement mainstream sequencing methods to investigate the levels of RNA molecules in biofluid samples, explore poorly characterized, rare transcripts and mutations. Cell-free RNA sequencing (RNA-seq) is a tool that extracts, processes, and analyzes cell-free RNA. We have developed a complete, automated workflow for performing cell-free RNA-seq. Our services are fully customizable to your research needs. cell free rna sequencing http s://rna.cd-genomics.c om/cell-free-rna-seq.html