Sizing & Quantitation
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About DNA Sequencing
The core application of the Micromon NGS facility is DNA sequencing. This 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 150 bases (and soon up to 450b). Insert sizes for paired-end sequencing can range from 200b to 5kb (we can produce 10kb and 20kb insert sizes for special circumstances)
How to use the DNA Sequencing Service
Forms and Resources
|Last Updated on Friday, 22 February 2013 00:43|