DNA sequencing based on intrinsic molecular charges
DNA sequencing based on intrinsic molecular charges
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DOI:
10.1002/anie.200503154
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发表时间:
2006-01-01
影响因子:
16.6
通讯作者:
Miyahara, Y
中科院分区:
文献类型:
--
作者:
Sakata, T;Miyahara, Y
Gene functional analyses have proceeded remarkably in the fields of molecular biology, pharmacogenomics, and clinical research, on the basis of completion of the decoding of the human genome. The analysis of nucleotide variation has become increasingly important for the assembly of a highresolution map of disease-related loci and for clinical diagnostics. The most common form of genomic variation is single-nucleotide polymorphism (SNP), which is an important marker in personalized medicine that affects disease susceptibility and resistance. Although a number of methods for SNP analysis have been developed,[1–7] DNA sequencing techniques still need to be improved in terms of cost, simplicity, and throughput to analyze not only SNPs but also genomic variations, such as insertion/deletion and short tandem repeats.We have been investigating a new approach to the direct, simple, and highly sensitive detection of nonlabeled molecular recognition events on a miniaturized and arrayed solidstate device.[8] Recently, several types of field-effect devices have been used for the electrochemical detection of hybridization events on a solid surface.[9] As DNA molecules are