Revolutionary Bioinformatics solution providing fast and accurate, client-specific analysis services.
Trust CAS with your BI analysis !
Highly optimized library preparation kit to be used with all Celemics ready-to-use or customized panels. Experience the incomparable efficiency and performance for NGS library preparation
Revolutionary Bioinformatics solution providing fast and accurate, client-specific analysis services.
Trust CAS with your BI analysis !
Highly optimized library preparation kit to be used with all Celemics ready-to-use or customized panels. Experience the incomparable efficiency and performance for NGS library preparation
Celemics’ comprehensive NGS panel for somatic cancer allows highly accurate and comprehensive analysis for identifying significant mutations and variants for solid tumors.
Utilizing NGS-based target enrichment methods for higher genotyping efficiency and accuracy. Providing cost-effective and optimized experiment compared to conventional methods, such as GBS, PCR and microarray in plant and animal research
Revolutionary Bioinformatics solution providing fast and accurate, client-specific analysis services.
Trust CAS with your BI analysis !
Utilizing NGS-based target enrichment methods for higher genotyping efficiency and accuracy. Providing cost-effective and optimized experiment compared to conventional methods, such as GBS, PCR and microarray in plant and animal research
Revolutionary Bioinformatics solution providing fast and accurate, client-specific analysis services.
Trust CAS with your BI analysis !
In-silico designed and wet-lab validated exclusive probes to ensure state-of-the-art capture performance
In-silico designed and wet-lab validated exclusive probes to ensure state-of-the-art capture performance
Revolutionary Bioinformatics solution providing fast and accurate, client-specific analysis services.
Trust CAS with your BI analysis !
Highly optimized library preparation kit to be used with all Celemics ready-to-use or customized panels. Experience the incomparable efficiency and performance for NGS library preparation
Revolutionary Bioinformatics solution providing fast and accurate, client-specific analysis services.
Trust CAS with your BI analysis !
Highly optimized library preparation kit to be used with all Celemics ready-to-use or customized panels. Experience the incomparable efficiency and performance for NGS library preparation
Celemics’ comprehensive NGS panel for somatic cancer allows highly accurate and comprehensive analysis for identifying significant mutations and variants for solid tumors.
Utilizing NGS-based target enrichment methods for higher genotyping efficiency and accuracy. Providing cost-effective and optimized experiment compared to conventional methods, such as GBS, PCR and microarray in plant and animal research
Revolutionary Bioinformatics solution providing fast and accurate, client-specific analysis services.
Trust CAS with your BI analysis !
Utilizing NGS-based target enrichment methods for higher genotyping efficiency and accuracy. Providing cost-effective and optimized experiment compared to conventional methods, such as GBS, PCR and microarray in plant and animal research
Revolutionary Bioinformatics solution providing fast and accurate, client-specific analysis services.
Trust CAS with your BI analysis !
In-silico designed and wet-lab validated exclusive probes to ensure state-of-the-art capture performance
In-silico designed and wet-lab validated exclusive probes to ensure state-of-the-art capture performance
Science is a collaborative process which works best when new knowledge is shared.
We contribute to this by presenting our research at scientific congresses and publishing our results in scientific journals.
Bae JM, Ahn JY, Lee H, Jang H, Han H, Jeong J, et al. Identification of tissue of origin in cancer of unknown primary using a targeted bisulfite sequencing panel. Epigenomics. 2022 May;14(10):615–28.
10.2217/epi-2021-0477
Lee C, Cheon KS, Shin Y, Oh H, Jeong YM, Jang H, et al. Development and Application of a Target Capture Sequencing SNP-Genotyping Platform in Rice. Genes (Basel). 2022 Apr 28;13(5):794.
DOI 10.3390/genes13050794
So MK, Ahn HK, Huh J, Kim KH. Germline pathogenic variants in unselected Korean men with prostate cancer. Investig Clin Urol. 2022 May;63(3):294–300.
DOI 10.4111/icu.20220044
Kim YM, Lee Y, Choi Y, Choi IH, Heo SH, Choi JM, et al. Clinical and genetic analyses of patients with lateralized overgrowth. BMC Med Genomics. 2022 Sep 30;15(1):206.
DOI 10.1186/s12920-022-01362-1
Kim K, Kim VN. High-throughput in vitro processing of human primary microRNA by the recombinant microprocessor. STAR Protoc. 2022 Mar 18;3(1):101042.
DOI 10.1016/j.xpro.2021.101042.
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