From Wikipedia, the free encyclopedia
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The term DNA sequencing refers to sequencing methods for determining the order of the nucleotide bases—adenine, guanine, cytosine, and thymine—in a molecule of DNA.
Knowledge of DNA sequences has become indispensable for basic biological research, other research branches utilizing DNA sequencing, and in numerous applied fields such as diagnostic, biotechnology, forensic biology and biologicalsystematics. The advent of DNA sequencing has significantly accelerated biological research and discovery. The rapid speed of sequencing attained with modern DNA sequencing technology has been instrumental in the sequencing of thehuman genome, in the Human Genome Project. Related projects, often by scientific collaboration across continents, have generated the complete DNA sequences of many animal, plant, and microbial genomes.
The first DNA sequences were obtained in the early 1970s by academic researchers using laborious methods based on two-dimensional chromatography. Following the development of dye-based sequencing methods with automated analysis,[1]DNA sequencing has become easier and orders of magnitude[clarification needed] faster.
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DNA Sequence Trace
|Contents |
| [hide] |
|1 History |
|2 Maxam–Gilbert sequencing |
|3 Chain-termination methods |
|3.1 Dye-terminator sequencing |
|3.2 Challenges |
|3.3 Automation and sample preparation |
|4 Large-scale sequencing strategies |
|5 New sequencing methods