•         

Pathogen Infections

Unravel Complex Infections with Precision NGS Solutions

Virus infection biotechnology concept illustration

In infectious-disease research and surveillance, identifying the causative agent is only the first step. Understanding its subtype, drug-resistance profile, and virulence potential drives meaningful breakthroughs. The Pathogen Infections NGS Panel series uses next-generation sequencing (NGS) to deliver comprehensive genomic characterization—going beyond detection to strain/subtype resolution, antimicrobial-resistance (AMR) marker assessment, and virulence analysis.
From hypothesis-free pathogen discovery to targeted analysis of defined organisms, this flexible portfolio supports studies of complex infections, accelerates epidemiological investigations, and informs preclinical therapeutic development.

Request a Quote

Vector of bacteria and pathogenic viruses

Sequencing-based infectious-disease research can be complex, but multiple NGS-based methods are available to improve workflow efficiency and data quality. Depending on sample requirements, single-genome, multi-pathogen, and discovery sequencing workflows provide a comprehensive set of solutions for microbiology and infectious-disease research.

Comprehensive pathogen Panel

Leveraging innovative probe design, our hybrid capture-based pathogen panel enables ultra-broad screening of bacteria, viruses, fungi, parasites, and other pathogens in research specimens.

Man inhaling airborne pathogen particles

Respiratory Pathogen NGS Panel

Accurate, rapid pathogen identification is critical for research breakthroughs and epidemic surveillance in complex respiratory infections. Our Respiratory Pathogen Detection Panel series, powered by Next-Generation Sequencing (NGS) technology, delivers robust solutions from broad-spectrum screening to precise typing – enabling efficient infection resolution and pathogen evolution tracking.

Oncovirus Precision Panel

Human papillomavirus HPV infection background

Investigate the role of oncogenic viruses (e.g., HPV, HBV, EBV) in cancer development, including mutation profiling and viral integration site analysis.

- CDCap™ HPV Panel - Covering full genomes of 222 HPV subtypes for genotyping, mutation profiling, and virus–host fusion site detection, can be spiked into exome panels for HPV-related tumor studies.

- CDCap™ HBV Panel - Designed from 5,500 full-length HBV genomes across 8 subtypes, HBV typing, mutation detection, and integration analysis.

- CDCap™ EBV Panel - Based on 304 full-length EBV genomes, EBV typing, mutation detection, and integration analysis.

Human embryonic stem cell rendering under microscope

Pathogen Detection & Sequencing Services: Precision in Microbial Studies

  • quick, cost-effective, ultra-sensitive, high-throughput testing solutions
  • Empower researchers to identify various pathogens, analyze pathogen mutations, and explore disease mechanisms efficiently
Click here to explore our full range of services

Why Choose Our Pathogen NGS Panels?

Our panels are engineered to overcome the most significant challenges in pathogen genomics: achieving high sensitivity amidst overwhelming host DNA, covering an immense breadth of targets, and delivering actionable data.

  • Unmatched Comprehensiveness: Our solutions range from ultra-broad panels covering over 7,000 pathogens to focused panels for key viruses like HPV, HBV, and EBV. This allows you to choose the perfect tool for unbiased discovery or targeted surveillance.
  • Superior Sensitivity & Specificity: Proprietary host depletion and hybridization capture technologies efficiently remove background noise, enabling the detection of even trace amounts of pathogen genetic material in complex sample types like whole blood or tissue.
  • Actionable Genomic Insights: We deliver more than just identification. Our panels are designed for precise subtyping, detection of drug-resistance markers, and analysis of virulence factors, providing a complete picture of the pathogen's threat profile.
  • Exceptional Flexibility: Many of our panels feature on-demand customization options, allowing you to add probes for emerging threats or specific genes of interest. With compatibility across multiple sample types and sequencing platforms (Illumina & MGI), our solutions integrate seamlessly into your existing workflow.
Cat.no Product Brief Description Inquiry Basket
PNP001 CDCap™ Ultra-Comprehensive Pathogen Kit CDCap™ Ultra-Comprehensive Pathogen Kit employs probe hybridization capture to detect 7,000+ pathogens and >1,000 AMR/virulence genetic markers. Its ~8,000 probes minimize host background while ensuring broad, specific enrichment for preclinical research and epidemiology.
PNP002 CDCap™ Comprehensive Pathogen Kit CDCap™ Comprehensive Pathogen Panel: Hybridization capture-based NGS kit detecting 435 pathogens, including resistance/virulence markers for preclinical research.
PNP003 Multi-Respiratory Pathogen Kit Multi-Respiratory Pathogen Kit detects & genotypes nearly 100 respiratory pathogens (viruses like influenza, bacteria, fungi, mycoplasma, chlamydia) via hybridization capture or PCR enrichment. It enables co-detection, differentiates 200+ subtypes, tracks variants, and offers >99% coverage with customizable primers/probes for emerging threats, AMR, and virulence genes
PNP004 CDAmp™ MTBC+NTM Panel kit CDAmp™ MTBC+NTM Panel is Multiplex PCR solution that detects MTBC & 169 NTM species plus 49 drug resistance mutations across 14 anti-TB drugs in one assay. Enables comprehensive TB research and clinical management.
* For research purposes only, not intended for clinical diagnosis, treatment, or individual health assessments.

Explore Our Pathogen Infections:

Cat. No. Product Name Brief Description Inquiry Basket
PN008 CDCap™ HPV Panel Kit CDCap™ HPV Panel enables comprehensive detection and genotyping of all 222 HPV subtypes via capture-based NGS. Analyzes tissue, cell or plasma samples for genotypes, mutations, and viral integration sites.
PN009 CDCap™ HBV Panel Kit CDCap™ HBV Panel enables HBV genotyping, drug-resistance mutation detection, and host integration analysis via amplicon-based NGS. Covers 5,500 sequences across 8 HBV subtypes from tissue, cells, or plasma.
PN010 CDCap™ EBV Panel Kit CDCap™ EBV Panel enables EBV genotyping, mutation detection, and host integration analysis via hybridization capture NGS. Covers 304 full-length EBV genomes from tissue, cells, or plasma.
Copyright © 2025 CD Genomics. All rights reserved.
Top
0
Inquiry Basket