Sample Extraction
High-molecular-weight genomic DNA isolated from biological specimens and stabilized in high-purity suspension for deep sequencing.
CS-0427 | HMW DNA | QC PASS
Fluorescence Basecalling
Real-time optical channels capture four-color fluorophore emissions across high-density flowcell channels.
FLOWCELL 04 | 2×150 BP | LIVE
Digital Reads Processing
Parallel basecall streams mapped against reference genomes with quality score filtering and error correction.
Q30 93.1% | 2.4B READS
Variant Matrix Mapping
Comprehensive identification of single nucleotide variants, insertions, and structural genomic alterations.
GRCh38 | 4,182 VARIANTS | READY
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.
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.
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.
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.
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.
HMW DNA extraction, barcoding protocols, and flowcell priming diagnostics.
Turnkey MinION starter deployments and standardized wet-lab curriculum.
Immersive 12-week genomic data analysis residencies with certified competency.
From Biological Sample to Scientific Insight
A seamless four-stage trajectory engineered to deliver maximum data integrity, zero amplification artifact, and actionable results.
Sample Prep
HMW DNA/RNA extraction with strict fragment length selection (>50 kb). Fluorometric Qubit QC and agarose gel integrity verification.
Nanopore Basecalling
Single-molecule translocation through synthetic protein pores at 400 bp/s. Direct electronic voltage sampling at 4,000 measurements/sec per channel.
Computational Analysis
Raw ionic current squiggles translated via Dorado SUP neural models. Structural variant calling (Sniffles2), chromosomal phasing, and methylation profiling.
Research Insight
Publication-ready methylation heatmaps, de novo assembly graphs, chromosomal phasing, and full raw POD5 / FASTQ + BAM + VCF delivery packages.
We Study Plants
Decoding complex plant genomes, promoter motifs, and transcriptional signatures to engineer climate-resilient crops and secure future agricultural yields.
We Study Humans
Unlocking genetic blueprints and deep biomarker pathways to accelerate precision medicine, diagnostics, and breakthrough therapeutic discoveries.
We Study Animals
Advancing comparative genomics and molecular selection to optimize livestock health, breeding efficiency, and sustainable agricultural productivity.
We Study Microbes
Exploring complex microbial ecosystems and plant-microbe interactions to pioneer next-generation industrial and environmental biotech solutions.
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.