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Celemics Analysis Service
Trust CAS with your Bioinformatics Analysis
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 >Trust CAS with your Bioinformatics Analysis
NGS 기반의 분자 진단 기술은 빠른 속도로 발전하고 있습니다. NGS 기반의 분자 진단 기술은 실험적 측면의 기술 발전과 데이터를 분석하는 기술의 발전이 같이 이루어져야 전반적인 발전을 이룰 수 있으나, 현재는 발전 속도에 다소의 차이가 있습니다.
실험 기술의 발전에 따라 다양한 새로운 바이오마커가 빠른 속도로 발굴되고 있으나 분석적 측면에서는 고객의 요구에 즉시 대응할 수 있는 솔루션이 거의 없습니다. 셀레믹스의 Celemics Analysis Service (CAS)은 복잡하고 제한적인 시장에서 고객 맞춤형 서비스를 제공하기 위해 개발된 혁신적인 생물 정보학 솔루션입니다. 실시간 고객 소통, 고객 요구에 따른 맞춤형 생물 정보학 분석 결과를 제공합니다.
CAS는 고객이 생물 정보학 분석에 대한 지식이 없더라도 분석 결과를 얻을 수 있도록 준비되어 있습니다. 고객의 실험 목적과 조건, 샘플의 상태에 따라 적합한 분석 방법을 제공할 수 있습니다 (Germline, Somatic, FFPE, cfDNA, RNA, 바이러스, 박테리아, Non-human Application, De-novo 시퀀싱, 메틸화 시퀀싱 등).
자동화된 BI 분석 파이프라인을 통한 분석을 포함해 비표준 분석에 이르기까지 모든 분석 과정과 결과는 셀레믹스의 BI 분석 전문가가 모니터링합니다. 분석 과정에 문제가 있을 경우 실시간 지원을 통해 고객 요구사항을 충족하기 위해 노력합니다.
셀레믹스는 GATK Best Practice 파이프라인을 따르며, 유럽 기반 서버를 사용하여 GDPR 기준을 만족합니다.
CAS는 고객의 연구 주제와 목적에 따라 최적화된 분석 서비스를 제공합니다.
고객 요청에 따라 결과 데이터 재분석 및 시각화 정보를 제공할 수 있으며, 고객 요청에 따라 별도의 다른 데이터베이스 정보를 주석으로 활용하는 옵션을 제공할 수 있습니다 (데이터베이스 정보에 대한 사전 사용 승인이 필요할 수 있습니다.)
셀레믹스의 BI 분석 전문가들은 고객과의 긴밀한 소통을 기반으로 표준 파이프라인 외에도 별도의 분석 파이프라인을 개발하는 것을 지원합니다.
FLT3-ITD Analysis:
visualized by IGV View
Gene Fusion Analysis from FFPE samples
NGS 데이터 분석에서 발생하는 어려움을 이해하고 있기 때문에, 셀레믹스의 분석 서비스 (CAS)는 무엇보다도 사용자 편의성을 높이는데 주력했습니다.
간단한 데이터 입력 인터페이스를 사용하여 고객별 맞춤 분석이 가능하도록 구성했기에 초기 세팅 비용 및 사용자 교육 시간을 절약할 수 있습니다. 고객의 분석 과정과 결과를 지속적으로 모니터링하여 문제 발생 시 실시간으로 해결할 수 있도록 지원하며 고객의 연구 상황에 따라 권장 분석법을 제공합니다.
Index Hopping과 같은 문제에 대해 지속적으로 모니터링하여 대안을 제공하며, 유럽 지역 내 서버를 사용하여 빠른 데이터 전송 속도와 짧은 전송 간격을 확보했습니다.
BI 분석 전문가가 분석을 도와드립니다. 계정 등록, 셋업 등의 별도의 과정이나 비용을 요구하지 않습니다.
고객이 원하는 분석 수준에 맞춰 결과를 제공합니다. 1차 (Primary), 2차 (Secondary), 3차 (Tertiary)의 세 단계로 나뉘며 Raw Data부터 Clinical Interpretation 리포트에 이르기까지 다양한 수준의 결과가 준비되어 있습니다.
셀레믹스는 유전변이에 대한 주석을 제공합니다. 유전자의 기능에 대한 연관성은 물론 진단, 예후 및 치료 계획과 관련이 있는지를 확인할 수 있습니다. 진단 및 예후와 관련한 자료는 AMP (미국 분자병리학회) 임상 지침과 연계한 자료를 제공합니다.
셀레믹스의 패널의 데이터 분석에 최적화되어 있습니다. 요청에 따라 사용자 친화적인 BI 분석 결과를 제공합니다.
01. Analysis Request
[Primary Analysis]
FASTQ to annotated VCF
[Secondary Analysis]
CNV, Large InDel, Fusion, TMB & MSI
[Tertiary Analysis]
Clinical Interpretation
[Provision of client]
Requested reports such as BAM/BAI, Annotated VCF, Performance Summary Statistics, Clinical Reports, etc.
Will require prior consultation and agreement.
[Variant Filtration]
Provision of process report for mutation detection using metrics such as VAF, depth, and strand conditions.
[Variant Clinical Significance]
Gathering relevant data types based on clinical information such as mutation type, protein functions, clinical database, etc.
After confirming the analysis request, a Celemics Bl expert will initiate and monitor the analysis
[Data upload]
On-site server or cloud server
[single click, automated upload]
05. Result Guidance
04. Request Interpretaion
03. BI Analysis
02. Data Transmission
Customer
CELEMICS
Customer
[Primary Analysis]
FASTQ to annotated VCF
[Secondary Analysis]
CNV, Large InDel, Fusion, TMB & MSI
[Tertiary Analysis]
Clinical Interpretation
[Data upload]
On-site server or cloud server
[single click, automated upload]
After confirming the analysis request, a Celemics Bl expert will initiate and monitor the analysis
[Variant Filtration]
Provision of process report for mutation detection using metrics such as VAF, depth, and strand conditions.
[Variant Clinical Significance]
Gathering relevant data types based on clinical information such as mutation type, protein functions, clinical database, etc.
[Provision of client]
Requested reports such as BAM/BAI, Annotated VCF, Performance Summary Statistics, Clinical Reports, etc.
Will require prior consultation and agreement.
01. Analysis Request
02. Data Transmission
03. BI Analysis
04. Request Interpretaion
05. Result Guidance
Protein-coding 영역을 폭넓게 포함하고 있으며, 높은 패널 성능과 BI 분석 솔루션을 기반으로 비용 효율적인 Exome 분석 가능
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 발생하는 유전변이까지 검출 가능
NGS Library Preparation 키트로 셀레믹스의 Target Enrichment 패널에 최적화된 키트