Blogs

Celemics SNP Genotyping and Targeted Sequencing SNP genotyping is a technology used to identify and analyze single nucleotide polymorphisms (SNPs) within the genome. SNPs are the most common form of genetic variation and play an important role in understanding disease susceptibility, drug response, and other genetic traits. SNP analysis is also widely applied in plant […]

Celemics Library Preparation Kit & Polymerase: Effect of High/Low GC-Ratio To conduct Next-Generation Sequencing (NGS), DNA sample must undergo a Library Preparation process tailored to the specific sequencing platform. Additionally, to perform further experiments like Target Enrichment, PCR is required to amplify the quantity of the library. However, the efficiency of this PCR process can […]

PDF Download NGS Sequencing Services Celemics provides reliable analytical results through sequencing services based on high-quality NGS panels applicable to various research fields, proven technology, and years of accumulated experience. Celemics’ NGS sequencing services are recommended for laboratories with limited NGS experience or difficulty operating their own equipment. 1. NGS Targeted Sequencing Service: Targeted sequencing […]

Celemics Influenza Virus Whole Genome Sequencing Service Respiratory viruses, especially RNA viruses like the influenza virus, exhibit high mutation rates, enabling them to rapidly form new variants By analyzing the whole genome of these viruses, researchers can obtain precise genetic information on viral strains, identify key gene mutations, and gain insights into viral evolution. This […]

Celemics Long-Read NGS Library Preparation & Target Enrichment Technology Since the introduction of the first Next-Generation Sequencing (NGS) instrument, numerous sequencing platforms with a variety of technologies have been developed. Along with their unique platforms, many NGS instrument companies such as Illumina, MGI, Thermo Fisher, PacBio, Oxford Nanopore, Singular Genomics, and Element Biosciences, have introduced […]

NGS (Next-Generation Sequencing) equipment is a technology used to rapidly analyze the nucleotide sequences of genomes. In this process, it is necessary to fragment the DNA samples into small pieces and attach universal primers to both ends of these DNA fragments. This process is known as NGS library preparation, and the primer binding sites are […]