Our Long-Read Sequencing service for full plasmid analysis offers a powerful solution for researchers seeking comprehensive insights into plasmid structures. Using advanced sequencing technologies, we provide accurate and complete sequencing of entire plasmids, including both circular and linear forms. Unlike short-read methods that may leave gaps or ambiguities in plasmid sequences, long-read sequencing ensures the generation of full-length, high-quality sequences, enabling a clearer understanding of plasmid size, gene content, regulatory regions, and potential structural variations.

Key Benefits:

• Complete Plasmid Sequencing: Obtain full, uninterrupted sequences of plasmids, capturing the entire genetic content in one read.
• Improved Structural Insights: Detect large structural variations, gene rearrangements, and complex regions that short-read technologies might miss.
• Accurate Identification of Plasmid Features: Identify antibiotic resistance genes, replication origins, and other functional elements with high precision.
• Enhanced Assembly and Mapping: Achieve superior plasmid assembly with minimal gaps, even for complex plasmids.
• High-Throughput Capability: Process multiple plasmids in parallel for large-scale studies with a fast turnaround.

This service is ideal for plasmid characterization in synthetic biology, microbiology, and genetic engineering, providing you with an in-depth understanding of plasmid sequences that supports your research, strain development, or therapeutic applications. Whether you’re working with plasmids in clinical, environmental, or laboratory settings, our Long-Read Sequencing ensures you get the most complete and reliable data possible.

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
  • Raw data ( text sequences & quality scores (.fastq file)
  • Consensus sequence (.fasta) from proprietary auto-assembly pipeline and table with consensus base quality and coverage at each position of the consensus (.tsv and xlsx)
  • Plasmid graphical map & annotations (pLannote file)
  • Alignment (.bam) against your reference sequence in case you provided us with a reference sequence in .fasta format and table of all variants detected by comparison to your reference sequence (.tsv and xlsx files)