The Sanger method is the technology that allowed us to sequence the first human genome, completed in 2003. We've come a long way since then, but when Frederick Sanger et al developed a chain-termination method for DNA sequencing back in 1977 it soon became the most popular method of choice for many many years. Sanger employed dideoxynucleic acids, ddNTPs, in addition to deoxynucleic acids together in the amplification of DNA during the Polymerase Chain Reaction (PCR). Instead of amplifying a section of DNA, the ddNTPS would cause amplification to terminate in a random number of amplified products. This new approach used fewer toxic chemicals and lower amounts of radioactivity than previously used techniques and because of its comparative ease, the Sanger method was soon automated and is still used to this day.
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