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We have developed a sequencing method based on the RNA polymerase chain termination reaction with rhodamine dye attached to 3'-deoxynucleoside triphosphate (3'-dNTP). This method enables us to conduct a rapid isothermal sequencing reaction in <30 min, to reduce the amount of template required, and to do PCR direct sequencing without the elimination of primers and 2'-dNTP, which disturbs the Sanger sequencing reaction. An accurate and longer read length was made possible by newly designed four-color dye-3'-dNTPs and mutated RNA polymerase with an improved incorporation rate of 3'-dNTP. This method should be useful for large-scale sequencing in genome projects and clinical diagnosis.
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Nobuya Sasaki
Kitasato University
Masaki Izawa
Japan Science and Technology Agency
Masanori Watahiki
Toyama Institute of Health
Proceedings of the National Academy of Sciences
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Sasaki et al. (Tue,) studied this question.
synapsesocial.com/papers/6a22fe1bd6da8eab4757ee4c — DOI: https://doi.org/10.1073/pnas.95.7.3455
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