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)