Long Read Sequencing
Long-read sequencing using Oxford Nanopore Technologies P2 Solo instruments.
We operate two P2 Solo instruments from Oxford Nanopore Technologies, paired with powerful computing infrastructure capable of running live super-accuracy basecalling. Nanopore sequencing is rapidly becoming the de facto method for long-read sequencing, offering increasingly competitive quality at affordable prices, while enabling applications that are difficult or impossible with traditional short-read technologies.
Oxford Nanopore enables real-time, long-read sequencing of native DNA and RNA molecules, opening applications that short-read platforms simply cannot match.
Sequencing Beyond Short Reads
Ultra-Long Reads
Complete assemblies, structural variant detection, and difficult genome resolution.
Native DNA & RNA
Direct molecule sequencing for epigenetics and RNA modification detection.
Real-Time Analysis
Live basecalling and adaptive workflows for rapid, time-sensitive results.
Flexible Throughput
Scalable from small pilot studies to large-scale sequencing projects.
Full-Length Isoforms
Alternative splicing, fusion transcripts, and isoform discovery across full-length reads.
Comprehensive Services
We offer end-to-end sequencing services, ensuring a seamless experience.
Extraction
High-quality nucleic acid extraction for robust downstream applications.
Library Preparation
Customized library preparation for your specific research needs.
Sequencing
Reliable and high-throughput sequencing for a wide range of applications.
Bioinformatics
Comprehensive data analysis tailored to your research goals.
Applications
Our Oxford Nanopore platform supports a broad range of long-read sequencing applications.
Microbial & Plasmid Genomics
Metagenomics
Transcriptomics
Epigenetics & Modifications
Targeted Sequencing
Advanced Genomics
And Many More
Let us know your project requirements!
Ready to Start Your Project?
Contact us today to discuss how our Oxford Nanopore sequencing platform can support your research.