Mitochondrial DNA Long read SMARTSeq

45,00

Select the number of each type of sample you want to sequence.

Description

Our Long-Read Sequencing service for full mitochondrial DNA analysis offers a powerful solution for researchers seeking comprehensive insights into mitochondrial DNA variations. Using advanced sequencing technologies, we provide accurate and complete sequencing of entire mitochondrial DNA. Unlike short-read methods that may leave gaps or ambiguities in mitochondrial sequences, long-read sequencing ensures the generation of full-length, high-quality sequences, enabling a clearer understanding of mitochondrial DNA variations,from SNPs to large structural variations to evaluate mitochondrial heteroplasmy.

Key Benefits:

  • Complete Litochondrial genome Sequencing: Obtain full, uninterrupted sequences of mitochondiral genome, 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.
  • Enhanced Assembly and Mapping: Achieve superior mitochondrial assembly with minimal gaps
  • High-Throughput Capability: Process multiple mitochondrial genomes in parallel for large-scale studies with a fast turnaround.

This service is ideal for mitochondrial characterization. Whether you’re working with mitochondrial DNA in Clinical, or Research settings, our Long-Read Sequencing ensures you get the most complete and reliable data possible.

Ask SMARTLife for the whole mitochondrial genome 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)
    • 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)