DNA Sequencing
Micromon Genomics offers a full suite of DNA sequencing applications. These can be used for resequencing, de novo assembly of genomes or other genetic elements, gene discovery, identification of genome variation (SNP identification, genome rearrangements, insertions and deletions), and more.
We can produce single or paired reads with read lengths ranging from 50 to 400 bases, and synthetic long reads covering kilobases to megabases. Contact us to discuss your project adn we can assist you with the most appropriate experimental design to answer your research questions.
We also offer a comprehensive QC service to evaluate your samples (or your sequencing libraries) before library construction.
How to use our NGS DNA Sequencing service
Simply download the Sample Submission Form, fill it in, and email it back to us. Then, deliver your sample labelled as per your submission form. We'll enter your sample into our QC process and commence library preparation. You will receive an email when we receive your sample, when your sample is ready for sequencing, and when your sequencing is complete. Finally, when your data is ready, we will send you the details required to download your data from your dedicated result page on our website.
What to submit:
- A completed sample submission form
- 1ng to 2ug of DNA, depending on your application (contact us to discuss the requirements)
- Any QC information you have determined for your samples.
Further details can be found in our Sample Submission Guidelines for DNA sequencing... or just contact us to discuss your project requirements!
Sample preparation and submission guidelines