Our Long-Read Sequencing service provides a powerful, comprehensive solution for obtaining accurate, full-length sequences of plasmids and PCR-amplified regions, offering in-depth insights into your target genes, genomes, or plasmid structures. Using advanced sequencing technologies, we ensure the generation of high-quality, uninterrupted reads that eliminate gaps and ambiguities typically associated with short-read methods. Whether you’re analyzing plasmid sequences or amplified DNA regions, our service guarantees a clearer understanding of genetic content, structural variations, and other key features.

For Plasmid Sequencing: We offer accurate and complete sequencing of entire plasmids, including both circular and linear forms. This approach helps you uncover plasmid size, gene content, regulatory regions, and potential structural variations. Our service is ideal for plasmid characterization in synthetic biology, microbiology, and genetic engineering applications, ensuring that you obtain the most reliable and complete data possible.

For Amplicon/PCR Sequencing: Our service also provides full-length sequencing of PCR-amplified regions, offering an accurate view of your target genes. Long-read sequencing minimizes errors associated with repetitive regions, enabling reliable interpretation of complex genomic data. This is crucial for applications such as studying gene variants, microbial diversity, or specific genomic regions where precision and full-length coverage are essential.

Key Benefits:

• Complete and Uninterrupted Sequences: Whether for plasmids or amplicons, we provide full-length sequences that capture all genetic content in a single read, ensuring no gaps or ambiguities.
• Improved Structural Insights: Detect large structural variations, gene rearrangements, and complex regions that traditional short-read methods may miss.
• Accurate Identification of Features: For plasmids, identify antibiotic resistance genes, replication origins, and other key functional elements. For amplicons, accurately sequence difficult regions like repetitive or homopolymeric sequences.
• High-Resolution Detection: Detect rare mutations, insertions, deletions, and structural variations within plasmids or amplicons that could otherwise be overlooked.
• Simplified Data Analysis: With long-read sequencing, assembly is streamlined, reducing the need for complex error correction or post-sequencing refinement.
• Versatility for Various Applications: Ideal for plasmid characterization, gene variant analysis, metagenomic studies, microbiome research, and structural variant detection.

Ask SMARTLife for the whole plasmid sequencing of your sample :

• Local Team Ready to Listen to your projects
• Fast Service with 24-Hour Results Delivery
• Comprehensive and Understandable Bioinformatics Results