CD Genomics insists on offering high-quality next generation sequencing (NGS) services to researchers all over the world.
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.
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.
Genome sequencing is the methodology employed to employ high-throughput DNA sequencing techniques alongside advanced bioinformatics tools for the compilation and scrutiny of both the functional and structural constituents of an entire genome. This comprehensive approach facilitates the examination of individual disparities and distinctions within populations. Moreover, by executing de novo sequencing and leveraging bioinformatics methodologies, it becomes possible to derive genetic maps for various species.
The term "transcriptome" encompasses the entirety of transcripts generated by the cells or tissues of a particular species under specific conditions. Leveraging second-generation high-throughput sequencing, it becomes feasible to efficiently and extensively acquire sequence data pertaining to nearly all transcripts and information on differential gene expression within the tissues or organs of a specific species under particular conditions. This approach has found extensive utility across diverse domains, encompassing fundamental research, clinical diagnostics, and pharmaceutical research and development.
. Highly experienced and qualified personnel
. State-of-the-art instruments and cutting-edge technologies
. Stringent quality control
. Personalized NGS and customized bioinformatics solution to suit your research needs
Professional strategy design
. Broad range of applications
. Competitive price
Surfing to learn how we can help you achieve your research goals through NGS technologies. For more information, please contact us! Our industry-leading Ph.D.-level specialists are always dedicated to providing comprehensive support and technical troubleshooting as quickly as possible.