PRODUCTS
- Whole Exome Sequencing Panel NEW
  
  Whole Exome Sequencing Panel
  
  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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- NGS Target Enrichment Panel
  
  NGS Target Enrichment Panel
  
  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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- Customized NGS Panel
  
  Customized NGS Panel
  
  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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- Ready-to-Use NGS Panel
  Ready-to-Use NGS Panel
- Bioinformatics
  Bioinformatics
  
  Celemics Analysis Service
  Celemics Analysis Service
  
  Revolutionary Bioinformatics solution providing fast and
  accurate, client-specific analysis services.
  Trust CAS with your BI analysis !
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- Modular Accessories
  Modular Accessories
  
  Library Preparation Kit
  
  Double Stranded cDNA Synthesis Kit
  
  Double-stranded cDNA Synthesis Kit
  
  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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  Hybridization Enhancer
  
  Hybridization Enhancer
  
  Celemics exclusive enzymes and buffers for enhanced hybridization to ensure improved coverage and uniformity.
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  Clean-up Beads
  
  Clean-up Beads
  
  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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  Streptavidin Beads
  
  Streptavidin Beads
  
  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
  
  CeleNM^™ Bead
  
  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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  CLM Polymerase
  
  CLM Polymerase
  
  Celemics’ highly optimized polymerase ensures market-leading amplification efficiency and accuracy with minimized PCR bias and error rate.
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  Library Preparation Kit
  
  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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Product Navigator

Whole Exome Sequencing Panel

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 >
APPLICATIONS
Application for diverse research and clinical NGS solution
Application Navigator
Oncology

Celemics’ comprehensive NGS panel for somatic cancer allows highly accurate and comprehensive analysis for identifying significant mutations and variants for solid tumors.

Oncology

Celemics’ comprehensive NGS panel for somatic cancer allows highly accurate and comprehensive analysis for identifying significant mutations and variants for solid tumors.

Liquid Biopsy

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.

Biopharma Solutions

Celemics offers end-to-end NGS-based detection and discovery solutions for Biopharma, CRO, and Drug discovery research fields.

Inherited Diseases

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.

Pharmacogenomics

Celemics offers flexible choice of assessing extensive target regions associated with Pharmacogenomics for client-specific drug prescription and drug metabolism.

Virus Research

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.

Agrigenomics

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.

RNA Sequencing

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.

Epigenetics

Celemics provides comprehensive solution for DNA methylation sequencing with proprietary probes specifically designed for methyl-seq, enabling accurate detection of methylation sites.

Metagenomics Sequencing

Complete solution with flexible panel design for characterization and differentiation of a myriad of microbial species.

Antibody Discovery

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.

Bioinformatics

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.
SERVICES
- Whole Exome Sequencing Service NEW
  
  Whole Exome Sequencing Panel
  
  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 >
- Customized NGS Panel
  
  Customized NGS Panel
  
  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 >
- Sequencing Services
  Sequencing Services
  
  Ready-to-Use Panels
  
  Immune Repertoire Profiling
  
  High-Throughput Genotyping Service
  High-throughput Genotyping Service
  
  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 >
- Bioinformatics Services
  
  Celemics Analysis Service
  
  Revolutionary Bioinformatics solution providing fast and
  accurate, client-specific analysis services.
  Trust CAS with your BI analysis
  View Detail >
- Biopharma Solutions
  
  Biopharma Solutions
  
  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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- Custom NGS Assay Development
  
  Custom NGS Assay Development
  
  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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Whole Exome Sequencing Panel

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 >
RESOURCES
- Technical Resources
  
  Technical Resources
  
  Find useful information, insights and tools for your Celemics’ products and services
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- Publications
  
  Publications
  
  Explore the most up-to-date publications featuring Celemics’ products and services
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- Blogs
  
  Blogs
  
  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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- Videos
  
  Videos
  
  Explore a diverse range of engaging video content, from fascinating experiments showcasing cutting-edge research to heartfelt customer testimonials.
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Technical Resources

Find useful information, insights and tools for your Celemics’ products and services
View Detail >
COMPANY
- About Us
  
  About Us
  
  Introducing Celemics, your trusted partner for NGS solutions
  View Detail >
- Technology
  Technology
  
  Probe Design Technology
  
  Probe Manufacturing
  
  Optimization
  
  Molecular Barcode
  
  Bioinformatics
  Probe Design Technology
  
  In-silico designed and wet-lab validated exclusive probes to ensure state-of-the-art capture performance
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- News & Events
  
  News & Events
  
  Stay up-to-date with the latest updates on our activities, events and achievements
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- Global Network & Partners
  
  Global Network & Partners
  
  Let’s change the NGS market together – our global presence and partners world-wide
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- Investors
  
  Investors
  
  Invest in sustainable success
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- Contact Us
  
  Contact Us
  
  Waiting for your experience with Celemics, an innovative leader in NGS industry
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About Us

Introducing Celemics, your trusted partner for NGS solutions
View Detail >

Publications

Celemics’ Publications

A null mutation of TNFRSF11A causes dysosteosclerosis, not osteopetrosis

Post category:Inherited Diseases
Post published:April 4, 2023

Front Genet

A null mutation of TNFRSF11A causes dysosteosclerosis, not osteopetrosis

Kırkgöz T, Özkan B, Hazan F, Acar S, Nalbantoğlu Ö, Özkaya B, et al. A Null Mutation of TNFRSF11A Causes Dysosteosclerosis, Not Osteopetrosis. Front Genet. 2022;13:938814.

DOI 10.3389/fgene.2022.938814

View Detail >

Tags: 2022

Whole Exome Sequencing Panel

NGS Target Enrichment Panel

Customized NGS Panel

Celemics Analysis Service

Double-stranded cDNA Synthesis Kit

Hybridization Enhancer

Clean-up Beads

Streptavidin Beads

CeleNM™ Bead

CLM Polymerase

Library Preparation Kit

Whole Exome Sequencing Panel

Oncology

Oncology

Liquid Biopsy

Biopharma Solutions​

Inherited Diseases​

Pharmacogenomics​

Virus Research​

Agrigenomics​

RNA Sequencing​

Epigenetics​

Metagenomics Sequencing​

Antibody Discovery​

Bioinformatics​

Whole Exome Sequencing Panel

Customized NGS Panel

High-throughput Genotyping Service

Celemics Analysis Service

Biopharma Solutions

Custom NGS Assay Development​

Whole Exome Sequencing Panel

Technical Resources​

Publications​

Blogs​

Videos

Technical Resources

About Us

Probe Design Technology

News & Events

Global Network & Partners​

Investors​

Contact Us​

About Us​

Front Genet

A null mutation of TNFRSF11A causes dysosteosclerosis, not osteopetrosis

CeleNM^™ Bead

Biopharma Solutions

Inherited Diseases

Pharmacogenomics

Virus Research

Agrigenomics

RNA Sequencing

Epigenetics

Metagenomics Sequencing

Antibody Discovery

Bioinformatics

Custom NGS Assay Development

Technical Resources

Publications

Blogs

Global Network & Partners

Investors

Contact Us

About Us