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.