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Skip to 0 minutes and 8 seconds Once the polymerase chain reaction is complete and the target region has been amplified sufficiently, the sample is ready for additional assays that can analyse the region and look for any changes in the DNA code causing the patient’s phenotype. One of the most widely used assays is Sanger sequencing, named after the man who invented it, Frederick Sanger. In this method, the DNA is used as a template in order to generate a set of fragments that differ in length from each other by a single base. The bases at the end of each of these fragments are labelled with one of four different fluorescent dyes, one for each of the individual DNA bases.

Skip to 0 minutes and 39 seconds The fragments are then separated by their size, and the bases at the end are imaged as they pass a high powered camera. This creates an image representing the original sequence of the DNA, known as an electropherogram. Because of the high quality of the data produced and the ability to characterise the DNA sequence at the molecular level, Sanger sequencing is currently the gold standard genetic test. The next section will show you how the reaction works in more detail.

PCR to DNA sequence

We welcome back Matt, who will introduce you to an important and popular method which is used to obtain the genetic sequence of a small region of the genome: Sanger sequencing. This is named after its inventor, Fred Sanger, a British biochemist after whom the Sanger Institute in Cambridge is named.

To learn in more detail how Sanger sequencing works and enables us to read the genetic sequence at a specific site within the genome, you may wish to watch this animation on the yourgenome website.

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Genomic Medicine: Transforming Patient Care in Diabetes

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