The most comprehensive whole exome panel that covers the target regions of all major WES panels in the market. With our proprietary technologies, we provide industry-leading performance and efficiency with complete BI solution.
View Detail >
Hybridization-based target enrichment panel with our intrinsic probe design, rebalancing, and molecular barcode technologies to efficiently analyze not only hard-to-capture areas but also challenging samples, such as damaged DNA or RNA.
View Detail >
End-to-end customized target enrichment panel with assay optimization, validation and even complete BI support. Over 1,000 custom panels developed world-wide. White-labeled customized product for business expansion also available.
View Detail >
The most comprehensive whole exome panel that covers the target regions of all major WES panels in the market. With our proprietary technologies, we provide industry-leading performance and efficiency with complete BI solution.
View Detail >
The most comprehensive whole exome panel that covers the target regions of all major WES panels in the market. With our proprietary technologies, we provide industry-leading performance and efficiency with complete BI solution.
View Detail >
End-to-end customized target enrichment panel with assay optimization, validation and even complete BI support. Over 1,000 custom panels developed world-wide. White-labeled customized product for business expansion also available.
View Detail >
Providing NGS-based diagnostics solutions for biopharma companies. Celemics can develop and deliver a flexible customization and commercialization services while maintaining the market-leading performance for our clients interested in clinical and companion diagnostics.
View Detail >
Tailored-fit customized assay development from designing to validation run; including not only the custom panel design but also species-specific or sequencer-specific blockers, followed by reagent conditioning to optimize the individual experiment and sequencer.
View Detail >
The most comprehensive whole exome panel that covers the target regions of all major WES panels in the market. With our proprietary technologies, we provide industry-leading performance and efficiency with complete BI solution.
View Detail >
Find useful information, insights and tools for your Celemics’ products and services
View Detail >
Explore the most up-to-date publications featuring Celemics’ products and services
View Detail >
Sharing interesting stories about the world of NGS and how Celemics delivers the innovative NGS solutions to the world of science.
View Detail >
Explore a diverse range of engaging video content, from fascinating experiments showcasing cutting-edge research to heartfelt customer testimonials.
View Detail >
Find useful information, insights and tools for your Celemics’ products and services
View Detail >
Stay up-to-date with the latest updates on our activities, events and achievements
View Detail >
Let’s change the NGS market together – our global presence and partners world-wide
View Detail >
Waiting for your experience with Celemics, an innovative leader in NGS industry
View Detail >Inherited Diseases
BMC Medical Genomics A novel mutation in RNF216 gene in a Turkish case with Gordon Holmes syndrome Durmaz Çelik N, Erzurumluoğlu E, Özben S, Toprak U, Yorulmaz G, Artan S,…
Genes Genotypic Profile and Clinical Characteristics of CRX-Associated Retinopathy in Koreans Kim DG, Joo K, Han J, Choi M, Kim S-W, Park KH, et al. Genotypic profile and clinical characteristics…
Korean J Ophthalmol Clinical and Genetic Findings in Korean Patients with Choroideremia Jo WG, Lee CS, Han J. Clinical and genetic findings in Korean patients with choroideremia. Korean J Ophthalmol.…
PloS one Novel THPO variant in hereditary thrombocytopenia: A potential candidate variant for predisposition to myeloid neoplasm Kwon SR, Kim MJ, Lee Y-E, Yun J, Jeong D-J, Park JH, et…
International Journal of Molecular Sciences The Genotype-Phenotype Correlation in Human 5α-Reductase Type 2 Deficiency: Classified and Analyzed from a SRD5A2 Structural Perspective Seo J, Shin S, Kim S-W, Kim SJ,…
Ann Pediatr Endocrinol Metab A Korean boy with a CHD8 mutation who presented with overgrowth, intellectual disability, and autism </h4 > Kim C, Noh E-S, Cho SY. A Korean boy…
Genes Clinical and Genetic Features of Korean Patients with Achromatopsia </h4 > Choi YJ, Joo K, Lim HT, Kim SS, Han J, Woo SJ. Clinical and genetic features of Korean…
BMC Medical Genomics Clinical and Genetic Analyses and Treatment Experiences of Patients with Lateralized Overgrowth Kim YM, Lee Y, Choi Y, Choi IH, Heo SH, Choi JM, et al. Clinical…
J Atheroscler Thromb Phenotypic and Genetic Analyses of Korean Patients with Familial Hypercholesterolemia: Results from the KFH Registry 2020 Kim H, Lee CJ, Kim SH, Kim JY, Choi SH, Kang…
Yonsei Med J Genetic Variants Associated with Adverse Events after Angiotensin-Converting Enzyme Inhibitor Use: Replication after GWAS-Based Discovery Lee CJ, Choi B, Pak H, Park JM, Lee JH, Lee SH.…
