Sanger Premium Sequencing
5,50€ – 384,00€
Select the number of each type of sample you want to sequence.
IMPORTANT : To sequence and analyse your samples, our laboratory needs all the details asked in the Sample Sheet.
1. Download and fill in the SampleSheet.
2. Drag & drop  SampleSheet + Reference below in case you have a Reference in fasta format (.fasta or .fa) available.
Providing us with a Reference improves the quality of the Bioinformatic analysis.
3. Place your order.
Description
Our Sanger Sequencing service allows you to submit your DNA sample and primers in separate tubes for sequencing. This flexible option is ideal for researchers who have custom primers or specific sequences they wish to use, while keeping the DNA and primers in separate containers. This service provides high-quality sequencing, ensuring precise and reliable results for a wide range of DNA analysis applications.
Key Features:
- High-Quality Results: We provide accurate, reliable sequencing with long read lengths, ensuring clear and precise identification of genetic variations, even in complex or challenging regions.
- Custom Primers: You provide the primers in a separate tube, and we incorporate them into the sequencing process. This allows for flexible, tailored sequencing based on your specific needs.
- Wide Application Range: This service is suitable for a variety of applications, including plasmid sequencing, PCR product analysis, gene fragment sequencing, and targeted sequencing for specific regions of interest.
- Efficient Process: We handle the sequencing with minimal effort on your part. Simply provide the DNA sample and primers in separate tubes, and we’ll take care of the rest to deliver high-quality sequencing results.
- Accurate Variant Detection: Ideal for detecting small genetic changes such as point mutations, SNPs, indels, or any sequence variations in targeted regions of DNA.