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NGS Pathogen Analysis Kit
Broad Pathogen Coverage · Streamlined Sample-to-Report Workflow · High Sensitivity in Complex Samples

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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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.
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Celemics exclusive enzymes and buffers for enhanced hybridization to ensure improved coverage and uniformity.
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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
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High-quality streptavidin bead that selectively isolates biotinylated ligands bound to hybridization probes; minimizing DNA loss during the target enrichment process.
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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.
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Celemics’ highly optimized polymerase ensures market-leading amplification efficiency and accuracy with minimized PCR bias and error rate.
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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
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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.
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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
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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.
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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.
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Find useful information, insights and tools for your Celemics’ products and services
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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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Find useful information, insights and tools for your Celemics’ products and services
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In-silico designed and wet-lab validated exclusive probes to ensure state-of-the-art capture performance
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Stay up-to-date with the latest updates on our activities, events and achievements
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Let’s change the NGS market together – our global presence and partners world-wide
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Waiting for your experience with Celemics, an innovative leader in NGS industry
View Detail >Broad Pathogen Coverage · Streamlined Sample-to-Report Workflow · High Sensitivity in Complex Samples
셀레믹스(Celemics)는 앰플리콘 기반(amplicon-based)과 하이브리디제이션(hybridization-based) 기반 타겟 농축 기술을 모두 제공할 수 있어 광범위한 병원체 NGS 솔루션이 가능합니다. 셀레믹스의 병원체 NGS 솔루션은 병원체 농도가 낮거나 샘플 복잡도가 높은 경우에도 바이러스, 박테리아, 곰팡이, 기생충 등의 병원체를 신뢰성 있게 검출 및 분석할 수 있습니다. 시료 준비부터 분석 리포트 생성까지 전체 워크플로우는 셀레믹스의 키트, 검증된 프로토콜, 자동화된 분석 파이프라인을 통해 완벽하게 지원됩니다.
셀레믹스의 병원체 패널은 낮은 입력량(low-input) 및 분해된 현장 샘플(degraded field samples)을 사용하여 분석 및 임상적 검증을 완료하였습니다. 병원체 농도가 낮은 어려운 샘플에서도 일관된 높은 유전체 커버리지를 확보하며, 다양한 바이러스 대상에 대해 신뢰성 있는 검출 한계(LOD) 성능을 입증했습니다.
(A) 다양한 바이러스 부하 조건에서의 뛰어난 민감도
앰플리콘 기반 패널은 인플루엔자 A/B와 같은 세그먼트 유전체 구조를 가진 바이러스에서도 HA(Segment 4), NA(Segment 6) 등 검출이 어려운 영역까지 포함해 뛰어난 커버리지를 제공합니다.
(B) 낮은 바이러스 부하의 임상 샘플에서도 검출 가능
하이브리디제이션 기반 패널은 변이율이 높은 유전체 영역 및 Ct 32 수준의 저농도 샘플에서도 90% 이상의 유전체 커버리지를 안정적으로 유지하였습니다.
Exceptional Sensitivity Across the Viral Load Spectrum
Influenza A

Influenza B

Influenza A - NA Segment
Celemics
Company I

* 1.2 M reads / sample
A
Respiratory Syndrome Panel

Hemorrhagic Fever Syndrome Panel

B
Celemics 병원체 패널은 단독 감염뿐만 아니라 동시 감염(co-infection) 및 숙주 유전체 오염 샘플에서도 높은 민감도를 유지합니다. 임상 및 환경 샘플 내 단일, 이중, 삼중 병원체 혼합 모델에 대해 모두 90% 이상의 유전체 커버리지를 확인하였습니다.
(A) 다중 병원체 검출
단일 및 다중 병원체가 포함된 샘플 모두에서 검출 성능을 검증하였으며, 다양한 바이러스 및 박테리아 병원체에 대해 90%이상으로 일관된 유전체 커버리지
(B) Celemics RSV Panel의 커버리지 성능
임상적으로 중요한 다양한 호흡기 병원체에 대해 반복 검증을 통해 확인된 90%이상의 일관된 높은 커버리지
Multiple Pathogen (Co-Infection) of Fever Syndrome Panel
Single Pathogen - Viruses

Single Pathogen - Bacteria

2 pathogens

3 pathogens

A
RSV A

RSV B

* The resulting reads were downsampled to 0.6 million per sample for analysis
B
셀레믹스는 앰플리콘(Amplicon) 및 하이브리디제이션(Hybridization) 기반 타겟 농축 기술을 모두 제공하며, 병원체 특성, 샘플 복잡도, 분석 목적에 따라 최적의 방식을 선택할 수 있습니다. 앰플리콘 방식은 이미 알려진 병원체의 빠르고 비용 효율적인 고처리량 검출에 적합하며, 하이브리디제이션 방식은 넓은 커버리지, 변이 내성, 복잡하고 저품질 샘플에서도 안정적인 성능을 제공합니다.
아래의 비교를 통해 연구자들은 자신의 연구 목적에 가장 적합한 타겟 농축 기술을 쉽게 선택할 수 있습니다.
| 앰플리콘 기반 | 하이브리디제이션 기반 | |
|---|---|---|
| 주요 특성 | 알려진 타겟 영역의 빠른 증폭 | 새로운 병원체 및 복잡한 시료 분석 가능 |
| 주요 적용 | 변이 분석, 고처리량 검출 | 다양한 병원체 식별, 복합 시료 분석 |
| 민감도 | 매우 높음 (저농도 타겟에 적합) | 높음 (복잡하고 희박한 시료에 적합) |
| 변이 내성 | 낮음 (프라이머 결합부위 변이에 민감) | 매우 높음 (프라이머 비의존적) |
| 유연성 | 제한적 (프리디자인 프라이머 기반) | 매우 유연 (타겟 확장 용이) |
| 소요 시간 | 빠름 (~1일 이내) | 중간 (1~2일) |
| 비용 효율성 | 알려진 타겟에 매우 효율적 | 복잡한 대규모 타겟 분석에 효율적 |
셀레믹스는 사용자가 FASTQ 파일을 업로드하는 것만으로 시퀀싱 품질 평가 및 병원체 및 변이 검출 결과를 시각화된 리포트 형태로 확인할 수 있는 자동화된 분석 솔루션을 제공합니다.

Data
Upload
Automated
Analysis
Visualized
Report
셀레믹스는 연구 목적에 맞춰 유전자, 유전체 영역 또는 병원체 전체를 타겟에 추가할 수 있는 맞춤 설계를 지원합니다. 인수공통감염병 추적, 환경 모니터링, 백신 개발 등 다양한 연구 목적에 따라 패널을 자유롭게 구성할 수 있으며, 미토콘드리아 또는 인트론 영역 삽입도 요청 가능합니다.
셀레믹스의 키트는 간소화된 실험 프로토콜을 제공하며, 라이브러리 제작 및 타겟 농축에 별도의 특수 장비가 필요하지 않습니다. 장비 보유 여부와 관계없이 다양한 실험 환경에서 손쉽게 도입할 수 있습니다.

1.Sample Input
(DNA/RNA)
3.Sequencing
Compatible with All
Sequencing Platforms
Data Upload &
Automated Bioinformatics Analysis
→ Visualized Report
& Consensus Genome Output
4.Analysis
2-1.Amplicon-based
2-2.Hybridization-based
Target
Amplification
Target
Enrichment
Library
Preparation
Library
Preparation

1.Sample Input
(DNA/RNA)
Hybridization-based

Target
Enrichment
Library
Preparation
Amplicon-based

Library
Preparation
Target
Amplification
Compatible with All
Sequencing Platforms

3.Sequencing
Data Upload &
Automated Bioinformatics Analysis
→ Visualized Report
& Consensus Genome Output

4.Analysis
| Pathogen | Influenza A/B Virus | Respiratory syncytial Virus A/B | Human Metapnuemovirus A/B |
|---|---|---|---|
| Target Region | Whole genome | Whole genome (>98%) | Whole genome (>98%) |
| Enrichment Method | Multiplex PCR | ||
| Hands-on Time | 2.5 hr (Assay Time 8 hrs) | ||
| Sample Type | Sputum, nasopharyngeal and oropharyngeal swabs and aspirate, tissue samples, and other methods for viral RNA sampling. | ||
| Bioinformatics Pipeline |
FASTQ to VCF Consensus genome sequence Analysis report | ||
Comprehensive Respiratory Virus Panel
| Target Viruses* | 9 types / 39 virus strains, including SARS-CoV-2 |
|---|---|
| Target Size | 706 Kb |
| Mutation Analysis | Variant detection, Viral mutation (SNV, Indel) from generated Whole Genome Sequence |
| Sample Type | URT, NP/OP, etc. |
| Platform | All Illumina and Thermo Fisher Scientific Sequencers |
| Kit Composition | Provides all required reagents, including RNA to cDNA kit, cDNA to captured library kit, and bioinformatics SW |
| Bioinformatics Pipeline | Stand-alone bioinformatics SW 'Celemics Virus Verifier' (FASTQ to Visual Report) |
African Swine Fever Virus Panel
| Target Viruses* | ASFV 26 strains |
|---|---|
| Target Size | 192 kb |
| Mutation Type | Virus detection, Virus genome assembly |
| Sample Type (amount) | Swine Blood (> 50 ng of fragmented DNA) |
| Platform | All sequencers from Illumina, Thermo Fisher, MGI, PacBio, and Oxford Nanopore |
| Bioinformatics Support | Celemics Virus Verifier (Detection report) |
Highly optimized, user- convenient NGS library preparation kit for all Celemics panels
Incomparable quality magnetic bead for simple, flexible, and reproducible purification
Respiratory Virus Comprehensive analysis of 9 different virus types, 39 strains of clinically significant respiratory viruses
Virus Accurate identification of various ASFV strains in a single NGS reaction with species-specific blocker

NGS Library Preparation 키트로 셀레믹스의 Target Enrichment 패널에 최적화된 키트

최고 품질의 마그네틱 비드로 사용하기 편리하며 높은 재현성을 보여 NGS 실험에 최적화된 비드

임상 진단을 위한 9가지의 다른 바이러스형 확인과 39가지의 균주 확인이 가능한 패널

한번의 테스트로 다양한 ASFV 균주의 정확한 확인이 가능한 패널
Technical Resources
[Product Overview] Celemics NGS Solution for Pathogen Research
Targeted Pathogen NGS Solutions : Celemics Amplicon Panels
Hybridization-Based Pathogen Enrichment Solution Customer Success Case: Unexplained Rash with Fever Syndrome Panel
Hybridization-Based Pathogen Enrichment Solution Customer Success Case: Unexplained Infectious Respiratory Syndrome Panel
Hybridization-Based Pathogen Enrichment Solution Customer Success Case: Unexplained Hemorrhagic Fever Syndrome Panel
Celemics Products & Services