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本文引用的文献

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3'-O-modified nucleotides as reversible terminators for pyrosequencing.作为焦磷酸测序可逆终止子的3'-O-修饰核苷酸。
Proc Natl Acad Sci U S A. 2007 Oct 16;104(42):16462-7. doi: 10.1073/pnas.0707495104. Epub 2007 Oct 8.
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Single-cell genomic sequencing using Multiple Displacement Amplification.使用多重置换扩增的单细胞基因组测序。
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The diploid genome sequence of an individual human.某个人类个体的二倍体基因组序列。
PLoS Biol. 2007 Sep 4;5(10):e254. doi: 10.1371/journal.pbio.0050254.
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Polony multiplex analysis of gene expression (PMAGE) in mouse hypertrophic cardiomyopathy.小鼠肥厚型心肌病中基因表达的聚合酶链式反应多重分析(PMAGE)
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Genome-wide mapping of in vivo protein-DNA interactions.体内蛋白质-DNA相互作用的全基因组图谱绘制。
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Detecting SNPs using a synthetic nanopore.使用合成纳米孔检测单核苷酸多态性。
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Nanopore sequencing technology: nanopore preparations.纳米孔测序技术:纳米孔制备
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Four-color DNA sequencing by synthesis using cleavable fluorescent nucleotide reversible terminators.使用可切割荧光核苷酸可逆终止子通过合成进行的四色DNA测序。
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Whole-genome re-sequencing.全基因组重测序
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Nanopore sequencing technology: research trends and applications.纳米孔测序技术:研究趋势与应用
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下一代测序技术的最新专利与进展

Recent Patents and Advances in the Next-Generation Sequencing Technologies.

作者信息

Lin Biaoyang, Wang Jun, Cheng Yin

机构信息

The Institute for Systems Biology, Seattle, WA, 98021 USA.

出版信息

Recent Pat Biomed Eng. 2008;2008(1):60-67. doi: 10.2174/1874764710801010060.

DOI:10.2174/1874764710801010060
PMID:21709726
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3122325/
Abstract

We are now witnessing a new genomic revolution due to the arrival and continued advancements in the next-generation high-throughput sequencing technologies, which encompass sequencing by synthesis including fluorescent in situ sequencing (FISSEQ) and pyrosequencing, sequencing by ligation including using polony amplification and supported oligonucleotide detection (SOLiD), sequencing by hybridization in combination with sequencing-by-ligation and nanopore technology, nanopore sequencing and other novel sequencing technologies using nano-transistor array, scanning tunneling microscopy and nanowire molecule sensors etc. We review here major technologies and recent patents for achieving high-throughput, ultra-fast, extremely cheap, and highly accurate sequencing. We will see enormous impacts of these next-generation sequencing methods for solving complex biological problems and for ushering in the practice of personalized medicine.

摘要

由于新一代高通量测序技术的出现及其持续发展,我们正在见证一场新的基因组革命。这些技术包括基于合成的测序,如荧光原位测序(FISSEQ)和焦磷酸测序;基于连接的测序,如使用克隆扩增和支持寡核苷酸检测(SOLiD);结合连接测序和纳米孔技术的杂交测序、纳米孔测序,以及其他使用纳米晶体管阵列、扫描隧道显微镜和纳米线分子传感器等的新型测序技术。我们在此回顾实现高通量、超快速、极其廉价和高精度测序的主要技术及近期专利。我们将看到这些新一代测序方法对解决复杂生物学问题和推动个性化医疗实践产生的巨大影响。