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BioPharma Solutions
NGS-based detection and discovery solutions for Biopharma, CRO and Drug discovery research fields
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 >Revolutionary Bioinformatics solution providing fast and
accurate, client-specific analysis services.
Trust CAS with your BI analysis !
Celemics offers easy-to-use kit with all components needed from RNA fragmentation to double-stranded cDNA synthesis suitable for NGS.
View Detail >Celemics exclusive enzymes and buffers for enhanced hybridization to ensure improved coverage and uniformity.
View Detail >Proven market-leading purification and size selection efficiency supported by Celemics’ unique magnetic bead-based chemistry. Compatible with all Celemics’ panels as well as other NGS providers
View Detail >High-quality streptavidin bead that selectively isolates biotinylated ligands bound to hybridization probes; minimizing DNA loss during the target enrichment process.
View Detail >CeleNM™ Bead streamlines library quantification and normalization in Next-Generation Sequencing (NGS). Say goodbye to traditional QC processes, saving time and costs while ensuring robust results. Experience uniform sequencing data distribution and comparable on-target ratios with CeleNM™ Bead.
View Detail >Celemics’ highly optimized polymerase ensures market-leading amplification efficiency and accuracy with minimized PCR bias and error rate.
View Detail >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
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 >Celemics’ comprehensive NGS panel for somatic cancer allows highly accurate and comprehensive analysis for identifying significant mutations and variants for solid tumors.
Celemics’ comprehensive NGS panel for somatic cancer allows highly accurate and comprehensive analysis for identifying significant mutations and variants for solid tumors.
Celemics has developed NGS ctDNA-based kits for colon, breast, and lung cancer assays. We have integrated our market-leading proprietary technologies and thoroughly validated and optimized as ready-to-use panels for clinical diagnostics.
Celemics offers end-to-end NGS-based detection and discovery solutions for Biopharma, CRO, and Drug discovery research fields.
In order to overcome the limitations of analyzing clinical diseases with conventional whole exome sequencing, Celemics introduces NGS-based clinical diagnostic solution for efficient detection of disease-causing variants for inherited diseases.
Celemics offers flexible choice of assessing extensive target regions associated with Pharmacogenomics for client-specific drug prescription and drug metabolism.
Celemics’ virus panels are designed to detect and identify disease-causing viruses. With our exclusive technologies, we provide efficient and accurate detection of targeted virus trains as well as procurement of credible data for whole viral genome sequencing.
To fulfill the expectations and growing needs for sequencing animals and plants, Celemics offers range of ready-to-use applicable to agrigenomics field as well as an option for developing customized NGS panel to specifically fit individual research purposes.
With Celemics’ proprietary technologies for assay development and optimization, we offer complete and robust NGS solutions for transcriptome, fusion, and isoform analyses for various sample types and conditions.
Celemics provides comprehensive solution for DNA methylation sequencing with proprietary probes specifically designed for methyl-seq, enabling accurate detection of methylation sites.
Complete solution with flexible panel design for characterization and differentiation of a myriad of microbial species.
Accurate and efficient analysis of IGH population that can detect MRD as low as 10-6 with optimized primers that can minimize sequencing loss and PCR duplications.
Celemics introduces revolutionary BI solution aiming to provide client-specific service. We provide fast, accurate, and sophisticated analyses of your NGS data accompanied by our proprietary bioinformatics pipeline.
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 >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
View Detail >
Revolutionary Bioinformatics solution providing fast and
accurate, client-specific analysis services.
Trust CAS with your BI analysis
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 >In-silico designed and wet-lab validated exclusive probes to ensure state-of-the-art capture performance
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 >NGS-based detection and discovery solutions for Biopharma, CRO and Drug discovery research fields
셀레믹스는 바이오파마에서 필요로 하는 NGS 기반의 시퀀싱 패널 개발 및 상업화 서비스를 지원할 수 있습니다. 환자군 분류, 임상 시험을 위한 대상자 선별은 물론 약물 개발과 관련한 마커 발견 등 관련 연구에 필요한 종합적이고 충분한 유전체 프로파일링 검사를 지원합니다. 독자적인 NGS 기술을 통해 바이오파마 분야의 다양한 영역에 효율적인 NGS 솔루션을 제공합니다.
초기 파일럿 테스트부터 상업화까지 전과정 지원 가능합니다. 셀레믹스는 파트너사의 국가가 요구하는 품질 요구 사항 및 규제 사항을 준수할 수 있도록 지원합니다. 또한, 엄격한 내부 검증 시스템을 거쳐 제품 출하되므로, 파트너 사가 보다 균일하고 정확한 품질의 제품, 서비스를 출시할 수 있도록 합니다.
철저하고 체계적인 제품 품질 관리 및 로트 관리는 성공적이고 정확한 임상 연구와 진단에 중요한 역할을 합니다. 셀레믹스에서는 패널의 생산부터 BI 분석 정보까지 생산된 모든 제품에 대해 상세한 기록을 유지하고 있습니다.
고객들에게 제품의 유효기간을 보증하는 문서를 제공할 수 있으며, 고객들의 연구와 진단 과정이 최상의 결과를 낼 수 있도록 지원합니다.
셀레믹스의 암 패널은 암과 밀접하게 관련이 있다고 알려진 유전자들로 구성되어 있습니다. 독점적인 프로브 및 패널 디자인 기술로 모든 종류의 변이, SNV, CNV, InDel 및 신규 변이를 검출할 수 있습니다.
CancerScreen 50 Panel |
CancerScreen Core Panel |
Biomarkers | FDA-approved anticancer agents targeting the corresponding gene |
---|---|---|---|
ALK (Fusion) | Crizotinib, Ceritinib, Alectinib, Lorlatinib | ||
BRAF | Dabrafenib+Trametinib, Vemurafenib+Cobimetinib, Encorafenib+Binimetinib | ||
EGFR | Gefitinib, Erlotinib, Afatinib, Osimertinib | ||
ERBB2 | Trastuzumab, Pertuzumab, Ado-trastuzumab, Emtansine, Neratinib | ||
KRAS | Sotorasib , Cetuximab, Panitumumab | ||
MET | Crizotinib | ||
NRAS | Cetuximab, Panitumumab | ||
PIK3CA | Alpelisib, Copanlisib, Duvelisib | ||
RET (Fusion) | Cabozantinib, Vandetanib, LOXO-292, BLU-667 | ||
ROS1 (Fusion) | Crizotinib, Ceritinib, Entrectinib | ||
FGFR3 | Erdafitinib | ||
IDH1/2 | Ivosidenib, Enasidenib | ||
NTRK1 (Fusion) | Larotrectinib, Entrectinib | ||
PDGFRA | Imatinib |
셀레믹스에서는 Gene Add-on, Spike-in 등 패널 확장을 지원합니다. Ready-to-use 패널뿐만 아니라 기존에 디자인한 맞춤형 패널에도 지원됩니다. 원하는 유전자 영역을 기존의 패널에 추가로 넣을 수 있어 연구 확장성이 높으며, 완전히 새롭게 패널을 디자인하는 것보다 비용 및 시간을 절약할 수 있습니다. 또한 고객 요청에 따라 GC-rich, Homologous 영역도 시퀀싱 영역에 포함해 드립니다.
Specification | CancerScreen Core Panel | CancerScreen 50 Panel |
---|---|---|
Gene Count | 13 genes | 54 genes |
Genes | APC, BRAF, EGFR, ERBB2, KRAS, MET, NRAS, PIK3CA, SMAD4, TP53 Fusion : ALK, RET, ROS1 |
ABL1, AKT1, ALK, APC, ATM, BRAF, BRCA1, BRCA2, CDH1, CDK4, CDK6, CDKN2A, CSF1R, CTNNB1, DDR2, EGFR, ERBB2, ERBB4, ESR1, FGFR1, FGFR2, FGFR3, GNA11, GNAQ, GNAS, HRAS, IDH1, IDH2, JAK2, KDR, KIT, KRAS, MAP2K1, MET, MLH1, MTOR, MYC, MYCN, NOTCH1, NRAS, NTRK1, PDGFRA, PIK3CA, PTCH1, PTEN, PTPN11, RB1, RET, ROS1, SMAD4, SMO, SRC, STK11, TP53 Fusion : ALK , RET, ROS1, NTRK1 |
Target size | 61 kb + Rearrangement | 197 kb + Rearrangement |
Mutation type | SNV, Indel, CNV, Rearrangement | |
Sample type | FFPE, frozen tissue, cfDNA, RNA | |
Platform | All sequencers from Illumina, ThermoFisher, MGI, and PacBio | |
Bioinformatics pipeline | Primary, Secondary, and Tertiary analysis result - FASTQ to VCF, VCF to Clinical report |
Protein-coding 영역을 폭넓게 포함하고 있으며, 높은 패널 성능과 BI 분석 솔루션을 기반으로 비용 효율적인 Exome 분석 가능
높은 민감도를 바탕으로 고형암의 분자 유전적 특징을 확인하고자 할 때 유용한 패널
임상 수준에 사용할 수 있는 높은 정확도의 cfDNA 패널. 아주 낮은 빈도로 발생하는는 유전변이까지 검출 가능
Protein-coding 영역을 폭넓게 포함하고 있으며, 높은 패널 성능과 BI 분석 솔루션을 기반으로 비용 효율적인 Exome 분석 가능
셀레믹스에서 제공하는 BI 분석 서비스로 다양한 수준의 분석 결과 제공 가능