OXFORD NANOPORE TECHNOLOGY

Technology for modern genomics

CAS-NGS uses Oxford Nanopore sequencing to deliver flexible, real-time DNA and RNA analysis for research, diagnostics support, and capacity-building programs.

Oxford Nanopore sequencing at CAS-NGS

REAL-TIME SEQUENCING

Generate insights as your sequencing run progresses.

THE PLATFORM

Built for flexible, research-focused sequencing

Oxford Nanopore technology enables CAS-NGS to support projects that benefit from long reads, real-time data generation, and adaptable sequencing workflows.

CAS-NGS sequencing platform

Long-read capability

Sequence long fragments to improve genome assembly, structural variant detection, and characterization of complex regions.

Real-time insight

Generate data as sequencing progresses, supporting faster decisions and iterative research workflows.

Scalable workflows

Support pilot studies, routine sequencing, and training environments across different sample volumes and project requirements.

APPLICATIONS

Where the technology adds value

Flexible sequencing can support research, surveillance, bioinformatics, and practical genomics education.

01

Pathogen Surveillance

Support outbreak monitoring and microbial characterization with portable, responsive sequencing workflows.

02

Clinical Research

Enable targeted studies that benefit from long reads, rapid analysis, and adaptable run design.

03

Bioinformatics Integration

Pair sequencing output with analysis pipelines for interpretation, reporting, and downstream decision-making.

04

Training & Capacity

Use the platform in courses and internships to build practical genomics and data analysis skills.

FREQUENTLY ASKED QUESTIONS

Technology FAQ

Common questions about Oxford Nanopore sequencing and how CAS-NGS applies the platform to research, analysis, and training.

What is Oxford Nanopore sequencing?

It is a sequencing approach that reads nucleic acids by measuring signal changes as molecules pass through nanopores, enabling long-read and real-time data generation.

Why use long-read sequencing?

Long reads help resolve repetitive regions, structural variation, and full-length molecules that can be difficult to characterize with short-read methods.

Can CAS-NGS support data analysis?

Yes. CAS-NGS combines sequencing with bioinformatics support to help process, interpret, and present results clearly.

Is the platform suitable for training?

Yes. The technology is well suited for hands-on courses and internships because it exposes learners to both wet-lab workflows and real analysis outputs.

What kinds of projects fit this platform?

Applications include microbial genomics, targeted research studies, surveillance work, and projects that benefit from flexible, real-time sequencing.

How do I discuss a project with CAS-NGS?

Contact CAS-NGS to review your goals, sample type, timeline, and analysis needs so the workflow can be matched to your project.

READY TO GET STARTED?

Plan your sequencing project

Talk with CAS-NGS about platform fit, sample requirements, bioinformatics support, and training opportunities.