Development of a New DNA Sequencing Method: 3′-Ester Cleavage Catalyzed byTaqDNA Polymerase
Author:
Publisher
Informa UK Limited
Subject
Genetics,Biochemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/15257779908041636
Reference5 articles.
1. DNA polymerase fluorescent substrates with reversible 3′-tags
2. Use of levulinic acid in the protection of oligonucleotides via the modified phosphotriester method: synthesis of decaribonucleotide u-a-u-a-u-a-u-a-u-a.
3. The application of levulinic acid as protective group to the synthesis of tetradecaribonucleotide U-A-U-A-U-A-U-A-U-A-U-A-U-A via the modified phosphotriester method
4. 3′-Modified Nucleotides for DNA Sequencing Without Gel Electrophoresis
5. Catalytic editing properties of DNA polymerases.
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1. Enzymatic Cleavage of 3’-Esterified Nucleotides Enables a Long, Continuous DNA Synthesis;Scientific Reports;2020-05-05
2. Thermococcus sp. 9°N DNA polymerase exhibits 3′-esterase activity that can be harnessed for DNA sequencing;Communications Biology;2019-06-20
3. An Efficient Strategy for Sequencing-by-Synthesis;Journal of Nanoscience and Nanotechnology;2010-05-01
4. An extension-quenching-extension sequencing on a microarray;Talanta;2010-04-15
5. A new class of cleavable fluorescent nucleotides: synthesis and optimization as reversible terminators for DNA sequencing by synthesis †;Nucleic Acids Research;2008-02-07
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