Sanger method of DNA sequencing, 3D animation with narration
The DNA sequencing method developed by Fred Sanger forms the basis of automated "cycle" sequencing reactions today. Scaling up to sequence. In the 1980s, two key developments allowed researchers to believe that sequencing the entire genome could be possible. The first was a technique called polymerase chain reaction (PCR) that enabled many copies of DNA sequence to be quickly and accurately produced. The second, an automated method of DNA sequencing, built upon the chemistry of PCR and the sequencing process developed by Frederick Sanger in 1977. (DNAi Location: Genome > The Project > Putting it together > Animations > Sanger sequencing)
The first method of sequencing the genetic code was devised by Fred Sanger. To sequence the DNA, it must first be separated into two strands. The strand to be sequenced is copied using chemically altered bases. These altered bases cause the copying process to stop each time one particular letter is incorporated into the growing DNA chain. This process is carried out for all four bases, and then the fragments are put together like a jigsaw to reveal the sequence of the original piece of DNA.
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Fred Sanger outlines DNA sequencing.
The cycles of the polymerase chain reaction (PCR).
Polymerase chain reaction (PCR) enables researchers to produce millions of copies of a specific DNA sequence in approximately two hours. This automated process bypasses the need to use bacteria for amplifying DNA.
A gene is a discrete sequence of DNA nucleotides
Frederick Sanger received two Nobel prizes (in the same category), for his work on protein sequencing and DNA sequencing.
DNA polymerase (blue) makes many copies of DNA (red) in a cycle of the polymerase chain reaction (PCR).
Early sequencers used four different reactions to determine the placement of each of DNA's four bases - known as A, C, T & G - in the sequence.
Frederick Sanger talks about the results from sequencing human mitochondrial DNA.
Two sequencing techniques were developed independently in the 1970s. The method developed by Fred Sanger used chemically altered "dideoxy" bases to terminate newly synthesized DNA fragments at specific bases (either A, C, T, or G). These fragments are th
Frederick Sanger describes the use of computers in sequencing.