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DNA 测序技术:2006-2016 年。

DNA sequencing technologies: 2006-2016.

机构信息

McDonnell Genome Institute, Washington University, St. Louis, Missouri, USA.

出版信息

Nat Protoc. 2017 Feb;12(2):213-218. doi: 10.1038/nprot.2016.182. Epub 2017 Jan 5.

DOI:10.1038/nprot.2016.182
PMID:28055035
Abstract

Recent advances in the field of genomics have largely been due to the ability to sequence DNA at increasing throughput and decreasing cost. DNA sequencing was first introduced in 1977, and next-generation sequencing technologies have been available only during the past decade, but the diverse experiments and corresponding analyses facilitated by these techniques have transformed biological and biomedical research. Here, I review developments in DNA sequencing technologies over the past 10 years and look to the future for further applications.

摘要

近年来,基因组学领域的进展在很大程度上要归功于能够以越来越高的通量和越来越低的成本对 DNA 进行测序。DNA 测序于 1977 年首次推出,而新一代测序技术仅在过去十年中才得以应用,但这些技术所带来的多样化实验和相应分析已经改变了生物和生物医学研究。在这里,我回顾了过去 10 年中 DNA 测序技术的发展,并展望了未来的进一步应用。

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2
Coming of age: ten years of next-generation sequencing technologies.成年:下一代测序技术的十年
Nat Rev Genet. 2016 May 17;17(6):333-51. doi: 10.1038/nrg.2016.49.
3
An Incomplete Understanding of Human Genetic Variation.对人类基因变异的不完整理解。
通过光学基因组图谱揭示工程化诱导多能干细胞系中的基因组重排
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Evaluation of Low-Coverage Sequencing Strategies for Whole-Genome Imputation in Pacific Abalone .太平洋鲍鱼全基因组插补的低覆盖度测序策略评估
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5
Mapping-based genome size estimation.基于图谱的基因组大小估计
BMC Genomics. 2025 May 14;26(1):482. doi: 10.1186/s12864-025-11640-8.
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UnigeneFinder: An Automated Pipeline for Gene Calling From Transcriptome Assemblies Without a Reference Genome.UnigeneFinder:一种用于在没有参考基因组的情况下从转录组组装中进行基因识别的自动化流程。
Plant Direct. 2025 Apr 22;9(4):e70056. doi: 10.1002/pld3.70056. eCollection 2025 Apr.
7
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Int J Med Sci. 2025 Jan 21;22(4):903-919. doi: 10.7150/ijms.101219. eCollection 2025.
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A sequencing-based method for quantifying gene-deletion mutants of bacteria in the intracellular environment.一种基于测序的方法,用于定量细胞内环境中细菌的基因缺失突变体。
Front Microbiol. 2025 Jan 28;15:1487724. doi: 10.3389/fmicb.2024.1487724. eCollection 2024.
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Front Oncol. 2025 Jan 6;14:1513073. doi: 10.3389/fonc.2024.1513073. eCollection 2024.
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