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 seq https://rna.cd-genomics.com/polya-rna-seq.html

Total RNA sequencing (RNA-seq) is a next-generation sequencing (NGS)-based method to capture a comprehensive view of the transcriptome. We provide total RNA-seq to help you analyze coding RNAs and multiple forms of ncRNA, including long noncoding RNA (lncRNA), small nuclear (snRNA), small nucleolar (snoRNA), and other ncRNA species. total-rna-seq https://rna.cd-genomics.com/total-rna-seq.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. deep sequencing viral genomes https://www.cd-genomics.com/mi....crobioseq/viral-phag

We provide multi-locus sequence typing service to help you characterize isolates of microbial species and contribute to the study of SNP, resistance genes and virulence factors of strains. mlst analysis https://www.cd-genomics.com/mi....crobioseq/multi-locu

PacBio Iso-seq analysis enables the discovery of new genes, transcripts, and alternative splicing events. The full-length sequences improve genome annotation to identify gene structure, regulatory elements, and coding regions and serve as an ideal method to characterize transcript isoforms within targeted genes or across an entire transcriptome. isoform sequencing https://longseq.cd-genomics.co....m/full-length-transc