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Long-Read Sequencing Services

Empowering Deeper Insights with AMD Biotech & Sequegenics

AMD Biotech's Long-Read Sequencing Services harness the power of advanced long-read sequencing technology, providing researchers with highly accurate, contiguous reads that unlock complex genomic information. Partnering with Sequegenics, a leader in genomics solutions, AMD Biotech combines robust sequencing technology with Sequegenics' specialized expertise, ensuring that your research reaches new depths of precision and insight.


Why Choose Us for Long-Read Sequencing?

Choosing Long Read Sequencing

Long-read sequencing enables the analysis of complex genomic regions that are often inaccessible with traditional short-read methods. 

High Accuracy

Reduced error rates and high-quality data for variant calling and structural variant analysis.

Comprehensive Analysis

Ideal for resolving complex regions like repetitive sequences, structural variants, and GC-rich regions.

Extended Read Lengths

Generate highly contiguous reads that improve the assembly of reference genomes, gene fusions, and large structural rearrangements.

Our Simple Workflow

Consultation & Project Design

Initial discussion to determine project goals, sample requirements, and customization options with our experts.

Sample Preparation & Sequencing

High-quality sample extraction with our Auto-Mag HMW DNA Isolation kit that is meant for extended read length sequencing, optimized with Sequegenics protocols.

Data Analysis & Reporting

Customized bioinformatics analysis on either PacBio Revio or Oxford Nanopore systems, variant calling, and detailed data reporting through Sequegenics' robust pipelines.

Ongoing Support

Post-project support to ensure that you maximize insights from your sequencing data.