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.
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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.
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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.
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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 >
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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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Let’s change the NGS market together – our global presence and partners world-wide
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View Detail >Oncology
Epigenomics Identification of tissue of origin in cancer of unknown primary using a targeted bisulfite sequencing panel Bae JM, Ahn JY, Lee H, Jang H, Han H, Jeong J, et…
Genes Development and Application of a Target Capture Sequencing SNP-Genotyping Platform in Rice Lee C, Cheon KS, Shin Y, Oh H, Jeong YM, Jang H, et al. Development and Application…
Investig Clin Urol Germline pathogenic variants in unselected Korean men with prostate cancer So MK, Ahn HK, Huh J, Kim KH. Germline pathogenic variants in unselected Korean men with prostate…
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…
Star Protoc High-throughput in vitro processing of human primary microRNA by the recombinant microprocessor Kim K, Kim VN. High-throughput in vitro processing of human primary microRNA by the recombinant microprocessor.…
BIODIVERSITAS Genetic diversity and phylogenetic analysis of Khiew-Phalee chickens based on mitochondrial DNA cytochrome b gene sequences Phromnoi S, Lertwatcharasarakul P, Phattanakunanan S. Genetic diversity and phylogenetic analysis of Khiew-Phalee…
Cancer Genet Evaluation of hereditary/familial breast cancer patients with multigene targeted next generation sequencing panel and MLPA analysis in Turkey Bora E, Caglayan AO, Koc A, Cankaya T, Ozkalayci H,…
Veterinary World First report on molecular characteristics and risk factor analysis of Ehrlichia canis in dogs in Khon Kaen, Thailand Mitpasa T, Sarker BR, Macotpet A, Bupata PA, Sangmaneedet S,…
Scientific Reports Feasibility of targeted cascade genetic testing in the family members of BRCA1/2 gene pathogenic variant/likely pathogenic variant carriers Lee J, Ham JY, Park HY, Jung JH, Kim WW,…
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…
