What Is NGS

NGS, also known as high-throughput sequencing, is a DNA sequencing technology which has revolutionized genomic and molecular research and has influenced all fields of biological research, it has become increasingly prevalent in modern society. NGS allows us to sequence DNA and RNA much more accurately, quickly and cheaply.

Library sequencing is a technique that encompasses the initial step of attaching adapters, which include elements like index sequences, barcodes, and sequencing primer binding regions, to both ends of the desired target fragments. Subsequently, these prepared fragments are subjected to sequencing using a dedicated sequencer. In contrast, targeted sequencing is characterized by the selective capture of particular genes or regions of interest before the sequencing phase. Notably, the principal methods for executing targeted sequencing comprise hybrid capture and multiplex PCR.

NGS Services At CD Genomics

With our many years of experience, CD Genomics is a leading provider of NGS services to provide advanced sequencing and bioinformatics solutions for its global customers. Equipped with a wide array of state-of-the-art technologies and supported by a group of experienced professionals, CD Genomics is committed to offering a complete service including experimental design, DNA isolation, DNA fragmentation, library preparation, sequencing, and bioinformatics, as a result, we deliver rapid, cost-effective and high-quality results that enable researchers to achieve scientific breakthroughs.

We are offering both the Illumina sequencing platforms, PacBio Single Molecular Real-Time (SMRT) and Nanopore technologies to meet a broad range of research goals and your budget.

Our technologies and products have been validated through multiple partnerships with the academic institutes, diagnostic companies, and testing laboratories.