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Powered by Oxford Nanopore Technology

Unlocking Genomic Insights at the Speed of Life.

Practical long-read DNA sequencing, research-grade bioinformatics, and capacity-building solutions powered by Oxford Nanopore Technology.

LIVE RUNNING • PROMETHION 24
FLOW CELL QC: Q20+ ACTIVE
MEMBRANE VOLTAGE: -180 mV 02:14:33 400 BPS TRANSLOCATION
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Throughput / Flowcell
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Consensus Accuracy (Q20+)
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Record Read Length
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Basecall Turnaround
Comprehensive Genomics Ecosystem

Precision Long-Read Sequencing & Advanced Compute

Engineered for researchers and institutions requiring ultra-high molecular weight DNA resolution, direct epigenetic modifications, and GPU-accelerated basecalling pipelines.

Oxford Nanopore Platform

Long-Read DNA & RNA Sequencing

Direct single-molecule sequencing of ultra-long native DNA and native RNA strands. Zero PCR amplification bias, real-time base modification calling, and phased telomere-to-telomere genomic assemblies.

HMW DNA Extraction Direct RNA-Seq 5mC & 6mA Methylation Adaptive Sampling
N50 > 50,000 BP TARGET Explore Sequencing →
dorado_live_gpu_pipeline.sh
# Oxford Nanopore Super-Accuracy Dorado Basecalling $ dorado basecaller sup,5mCG_5hmCG pod5/ –device cuda:all ✔ Flow cell R10.4.1 loaded • 2,048 pore channels online → Real-time Q20+ filtered reads: 98.2% → Cumulative bases called: 84.9 Gb $ sniffles –input aligned.bam –vcf structural_variants.vcf ✔ Phased SV calls resolved across all chromosomes → Translocation events identified: 14 $ _
READ LENGTH DISTRIBUTION (N50: 42.8 KB)
GPU Compute Pipeline

Custom Bioinformatics Pipelines

End-to-end computational genomics run on dedicated NVIDIA GPU clusters. From Dorado Super-Accuracy basecalling to Sniffles2 structural variant discovery, phased diploid assemblies, and methylome profiling.

Dorado SUP Neural Models Sniffles2 SV Discovery Phased Diploid Assembly Full VCF / BAM / POD5
NVIDIA RTX 4090 CLUSTERS View Pipelines →
Institutional Enablement • RESIDENCY PROGRAM

Hands-On Capacity Building & Laboratory Training

Democratizing genomic knowledge by training the next generation of sequencing scientists. We partner with universities, government labs, and medical centers to stand up self-sufficient long-read genomics hubs.

Wet Lab Masterclasses

HMW DNA extraction, barcoding protocols, and flowcell priming diagnostics.

University Lab Training

Turnkey MinION starter deployments and standardized wet-lab curriculum.

Student Internships

Immersive 12-week genomic data analysis residencies with certified competency.

ACADEMIC & GOVERNMENT COHORTS View Training Modules →
Rigorous Pipeline

From Biological Sample to Scientific Insight

A seamless four-stage trajectory engineered to deliver maximum data integrity, zero amplification artifact, and actionable results.

PHASE 01

Sample Prep

HMW DNA/RNA extraction with strict fragment length selection (>50 kb). Fluorometric Qubit QC and agarose gel integrity verification.

PHASE 02

Nanopore Basecalling

Single-molecule translocation through synthetic protein pores at 400 bp/s. Direct electronic voltage sampling at 4,000 measurements/sec per channel.

PHASE 03

Computational Analysis

Raw ionic current squiggles translated via Dorado SUP neural models. Structural variant calling (Sniffles2), chromosomal phasing, and methylation profiling.

PHASE 04

Research Insight

Publication-ready methylation heatmaps, de novo assembly graphs, chromosomal phasing, and full raw POD5 / FASTQ + BAM + VCF delivery packages.

Accelerate Your Scientific Discovery

Ready to Start Your Sequencing Run?

From pilot project library preparation to full PromethION 24 flowcell cohorts and institutional pipeline deployments, our team is ready to scale your genomics workflow.