miRNA sequencing, based on next-generation sequencing (NGS), can comprehensively profile miRNA sequences, either known or novel miRNAs. Our miRNA sequencing detects novel miRNAs as well as isomiR, enabling you to see precisely which miRNA sequences are expressed in your samples and uncover the importance of these small regulatory elements linked to a wide range of biological functions. microrna-seq https://rna.cd-genomics.com/mirna-sequencing.html
We provide full-length 16S/18S/ITS rRNA service based on PacBio or Oxford nanopore sequencing platform for accurate microbial identification, molecular phylogeny, and functional profiling. 16s full length sequencing https://www.cd-genomics.com/mi....crobioseq/full-lengt
CD Genomics provides reliable and comprehensive TCR/BCR repertoire analysis for blood, bone marrow, or tissue samples based on long-read sequencing technology, PacBio SMRT sequencing. We can guarantee the consistency of the sequencing process and analysis results for each sample throughout the experiment, and perform detailed bioinformatics processing and data analysis of the sequenced data. bcr repertoire sequencing https://longseq.cd-genomics.co....m/full-lengthtcr-bcr
CD Genomics provides target area sequencing data analysis service. We use bioinformatics to deeply mine the target genes genetic information and mutation information based on the target area sequencing data. Our unique skills in data analysis can meet customers' personalized data analysis needs and provide the most comprehensive data analysis results. target capture sequencing https://bioinfo.cd-genomics.co....m/target-area-sequen
CD Genomics is now providing 2b-RAD sequencing which is a novel reduced-representation whole genome sequencing and restriction-site associated DNA (RAD) sequencing method for linkage mapping and determination of genome-wide variants in a cost-effective way. radseq https://www.cd-genomics.com/2b-RAD.html
