What is Oxford Nanopore Sequencing?

Oxford Nanopore Sequencing is a next-generation sequencing (NGS) technology that stands out for its unique approach to reading DNA sequences. Unlike traditional methods that rely on fluorescence or other detection methods, Oxford Nanopore Sequencing leverages nanopores – tiny, naturally occurring channels – to directly analyze DNA in real-time.

Why Choose Nanopore Sequencing?

Nanopore sequencing is a revolutionary technology that allows for direct, real-time analysis of DNA and RNA molecules. Unlike traditional sequencing methods, nanopore sequencing offers several advantages.

ONT long reads

Major Advantages Of Nanopore Sequencing

  • Long Read Lengths: Obtain complete and continuous sequences, enabling the detection of structural variants, complex regions, and full-length transcripts.
  • Real-Time Analysis: Monitor the sequencing process as it happens, allowing for rapid data acquisition and dynamic experimental adjustments.
  • Single Molecule Sequencing: Analyze individual DNA or RNA molecules, providing a more accurate representation of genetic diversity and heterogeneity.
  • Minimized Sample Requirements: Achieve robust results with lower input DNA/RNA amounts, preserving precious samples and expanding the range of applicable samples.

Why Choose 1010Genome?

At 1010Genome, we go beyond providing sequencing. Our team of skilled bioinformaticians and genomic analysts is dedicated to delivering actionable insights from your nanopore sequencing experiments.

Our Bioinformatics Services

At 1010Genome, we’re at the forefront of cutting-edge genomics, and our Oxford Nanopore Bioinformatic Services stand as a testament to our commitment to providing unparalleled insights into your genetic data.

Key Features of our Bioinformatic Services:

  1. Precision Analysis: Our services ensure precise and accurate analysis of your genomic data, providing valuable insights into genetic variations, structural variants, and more.
  2. Long-Read Sequencing: Benefit from the advantages of long-read sequencing, allowing for a more complete understanding of complex genomic regions, including repetitive sequences and structural variations.
  3. Comprehensive Data Interpretation: We go beyond mere data generation. Our team of expert bioinformaticians meticulously analyzes the data, offering comprehensive insights into the functional aspects of your genome.
  4. Customized Solutions: Recognizing that each project is unique, we tailor our services to meet your specific requirements, whether it’s genome assembly, variant calling, or metagenomic analysis.
  5. Scalable and Cost-Effective: Our bioinformatic services are designed to be scalable, accommodating projects of various sizes. We ensure a cost-effective solution without compromising on the quality and depth of analysis.

Why Choose 1010Genome For Your Nanopore Data?

One-Stop-Solution

Benefit from the expertise of our team with extensive experience in nanopore sequencing and bioinformatics.

Customized Solutions

Tailored analysis pipelines to meet the specific needs of your research project, providing flexibility and personalized insights.

Rapid Turnaround

We understand the importance of time in research. Our efficient workflows ensure timely delivery of high-quality results.

Cost Effective

We ensure a cost-effective solution without compromising on the quality and depth of analysis.

Unlock the Full Potential of your Genomic Projects with 1010Genome's Nanopore Sequencing & Bioinformatic Analysis Services.

Contact us today to discuss your project and discover how our expertise can elevate your genomic research.