Library Preparation Kit
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Optimized for high-efficiency Celemics Panels (Standard / EP)

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 >Incomparable quality magnetic bead for simple, flexible, and reproducible purification
Optimized for high-efficiency Celemics Panels (Standard / EP)
셀레믹스의 라이브러리 제작 키트(Library Preparation Kit)는 셀레믹스의 모든 패널에서 높은 효율로 NGS 라이브러리 제작이 가능하도록 최적화되어 있습니다.
Mechanical Fragmentation 방식을 사용하는 Standard Library Prep Kit (LP Kit)와 효소 기반의 Enzymatic Prep Kit (EP Kit)는 End-Repair/A-tailing 효소 믹스, 인덱스 프라이머(싱글 또는 듀얼), 어댑터, 버퍼 등 라이브러리 제작에 필요한 모든 시약을 포함하고 있어 사용자의 워크플로우를 간소화합니다.
셀레믹스는 연구기관, 병원, 진단 기업이 하나의 공급원을 통해 높은 라이브러리 수율, 우수한 재현성, 그리고 안정적인 시퀀싱 결과까지 얻을 수 있도록 지원합니다.

Standard Kit(Mechanical Fragmentation, LP Kit)은 일반적인 워크플로우를 따르며, 기계적(초음파 분해) 또는 효소적(fragmentase) 절단 후 End-repair, A-tailing, 어댑터 라이게이션, 인덱싱 PCR 단계를 거칩니다.
반면, EP Kit(Enzymatic Fragmentation)는 DNA 절단 과정을 End-repair/A-tailing 단계에 통합하여 별도의 절단 과정이 필요하지 않습니다.
이러한 유연성 덕분에 사용자는 실험실 환경에 따라 기존의 절단 장비를 활용하거나, 보다 단순화된 EP 프로토콜을 선택할 수 있습니다.
For Option 1, ultra sonicator is not provided with the kit.
For Option 2, the inclusion of the fragmentase in the kit is optional.
NGS Library Preparation | ||
|---|---|---|
Standard Fragmentation | EP Fragmentation | |
| Option 1. Sonication | Option 2. Fragmentase | FER / A |
| Bead Purification & Quantification | ||
| ER / A | ER / A | |
| Adapter Ligation (Single / Dual Index) | ||
| Bead Purification | ||
| Index PCR | ||
Target Enrichment | ||
셀레믹스의 라이브러리 제작 키트(Library Preparation Kit)는 최대 DNA 라이브러리 수율과 일관된 결과를 얻을 수 있도록 설계되었습니다. 비교 평가 결과, Standard Kit과 EP Kit 모두 높은 라이브러리 수율과 뛰어난 재현성을 보여주었습니다.
Five replicate libraries were prepared using 100 ng of input DNA to evaluate the reproducibility and yield performance of the Celemics LP and EP Kits. The LP Kit was tested with 8 PCR cycles and the EP Kit with 5 PCR cycles under identical conditions.
Both kits demonstrated consistent library yields across replicates, confirming high reproducibility, while the EP Kit showed higher overall yield efficiency.More uniform read depths over GC-rich regions compared to competitor products.


셀레믹스의 라이브러리 제작 키트는 폭넓은 GC 함량 범위에서 안정적인 증폭 성능을 제공합니다.
셀레믹스의 독자적인 CLM Polymerase가 적용되어, GC가 풍부하거나 부족한 유전체 영역 모두에서 우수한 증폭 균일성을 유지하고 PCR 편향을 최소화합니다.
서로 다른 GC 조성을 가진 세균 유전체를 대상으로 한 비교 연구에서도 CLM Polymerase는 일정하고 균형 잡힌 리드 커버리지를 보여주어, 염기 조성에 관계없이 고품질의 시퀀싱 데이터를 확보할 수 있음을 입증했습니다.
The amplification capacity was tested using bacterial samples with known GC contents. The results show that CLM Polymerase allows steady and uniform amplification without PCR bias for both high-GC and low-GC regions.
* For GC-ratio analysis, the genomic DNA sequence was partitioned into contiguous 200 bp fragments. The GC content of each fragment was computed, and the resulting values were aggregated into a histogram with 2% interval bins. The green, red, and purple lines represent the normalized sequencing depth across different GC-ratio regions.
셀레믹스의 LP 및 EP Kit은 플랫폼에 구애받지 않으며, 주요 NGS 장비 전반에서 검증되었습니다.
이 키트들은 Illumina, MGI 시퀀싱 플랫폼은 물론 Thermo Fisher의 Ion Torrent 시퀀서와도 완벽히 호환되도록 설계되어, 기존의 시퀀싱 환경이나 분석 파이프라인을 변경할 필요가 없습니다.
또한 셀레믹스의 Target Enrichment Panel과 함께 사용하면, 시료 준비부터 시퀀싱까지 완전히 최적화된 엔드-투-엔드(End-to-End) 워크플로우를 구현할 수 있습니다.
셀레믹스는 라이브러리 제작에 필요한 모든 구성품을 하나의 키트에 제공합니다.
추가 시약을 별도로 준비할 필요가 없어 프로토콜 설정이 간편하며, 인덱싱 프라이머는 싱글 및 듀얼 인덱스 형식으로 제공되어 다양한 처리량과 멀티플렉싱 요구를 충족합니다.
워크플로우는 완전히 자동화에 대응하도록 설계되어, Hamilton, Tecan, Beckman 등 일반적인 액체 취급 로봇 시스템에서도 구현할 수 있습니다. 이를 통해 고처리량의 자동화 프로세스를 실현할 수 있으며, 인력과 시간을 절약하면서도 높은 일관성을 유지할 수 있습니다.
이러한 올인원 및 자동화 친화적 설계는 소규모 연구실은 물론 대형 임상기관 및 코어 시설에도 이상적인 솔루션입니다

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

타겟 영역에 결합한 프로브를 Biotin-Streptavidin 결합력을 이용하여 농축하기 위해 사용되는 비드

유전 질환과 밀접하게 연관된 것으로 알려진 7,000여개의 유전자를 타겟할 수 있도록 디자인 된 패널
Technical Resources
[Product Sheet] Celemics Library Preparation Kit
Celemics Target Enrichment Panel Overview
Celemics Products & Services
Safety Data Sheets
최신 MSDS 파일이 필요하시면 ‘Contact Us‘를 통해 문의 주시기 바랍니다.
MSDS_Library Preparation Kit_Illumina
MSDS_Library Preparation Kit_Thermo Fisher
MSDS_Library Preparation Kit_MGI