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.
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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.
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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.
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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.
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Explore the most up-to-date publications featuring Celemics’ products and services
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Sharing interesting stories about the world of NGS and how Celemics delivers the innovative NGS solutions to the world of science.
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Explore a diverse range of engaging video content, from fascinating experiments showcasing cutting-edge research to heartfelt customer testimonials.
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Let’s change the NGS market together – our global presence and partners world-wide
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View Detail >Inherited Diseases
Scientific Reports Identification and analyses of exonic and copy number variants in spastic paraplegia Shafique A, Nadeem A, Aslam F, Manzoor H, Noman M, Wohler E, Witmer PD, Sobreira N,…
Annals of Pediatric Endocrinology & Metabolism Genetic evaluation using next-generation sequencing of children with short stature: a single tertiary-center experience Kim SJ, Joo E, Park J, Seol CA, Lee J-E.…
Genes Paternally Inherited Noonan Syndrome Caused by a PTPN11 Variant May Exhibit Mild Symptoms: A Case Report and Literature Review Han JY, Park J. Paternally inherited Noonan syndrome caused by…
Heliyon Novel compound heterozygous mutations in SCN4A as a potential genetic cause contributing to myopathic manifestations: A case report and literature review Han JY, Park J. Novel compound heterozygous mutations…
Korean Circulation Journal Clinical and Genetic Features of Korean Inherited Arrhythmia Probands Jeong JH, Oh S-K, Kim YG, Choi YY, Lee HS, Shim J, et al. Clinical and genetic features…
Ophthalmic Research Phenotypic and Genetic Alterations in Adult-Onset Cone and Cone-Rod Dystrophy Kim DJ, Woo SJ, Joo K. Phenotypic and genetic alterations in adult-onset cone and cone-rod dystrophy. Ophthalmic Res.…
Front. Genet Clinical and genetic features of Koreans with retinitis pigmentosa associated with mutations in rhodopsin Jung YH, Kwak JJ, Joo K, Lee HJ, Park KH, Kim MS, et al.…
Rev Assoc Med Bras Importance of targeted next-generation sequencing in pediatric patients with developmental epileptic encephalopathy Bariş S, Kırık S, Balasar Ö. Importance of targeted next-generation sequencing in pediatric patients…
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,…
