期刊文献+

微流控法DNA片段化研究进展 被引量:1

Recent Progress of DNA Fragmentation Based on Microfluidics
下载PDF
导出
摘要 DNA分子的片段化技术对于下一代基因测序技术和疾病检测技术意义重大,文章回顾了现有的DNA片段化方法,着重介绍了基于微流控芯片技术的流体动力学剪切法DNA片段化技术,总结了影响微流控芯片中DNA片段化过程的因素,并且展望未来微流控技术在DNA片段化和生物芯片领域的应用. DNA fragmentation is one of the key technologies for gene library and disease detection. Normal DNA fragmentation technologies are reviewed focusing on microfluidic based DNA fragmentation technology. Effective pa- rameters are discussed and summarized according to the resulted DNA fragments. The importance and perspective of microfluidic DNA fragmentation are summarized.
出处 《华南师范大学学报(自然科学版)》 CAS 北大核心 2016年第1期23-27,2,共5页 Journal of South China Normal University(Natural Science Edition)
基金 国家自然科学基金项目(51405165) 教育部“长江学者和创新团队发展计划”项目(IRT13064) 广东省引进创新科研团队计划项目(2011D039)
关键词 微流控 DNA片段化 流体剪切 基因测序 microfluidics DNA fragmentation fluidic shearing gene sequencing
  • 相关文献

参考文献22

  • 1EL MUSTAPHA B, STAMBROOK P J. Next-generation sequencing technologies: breaking the sound barrier of human genetics[ J]- Mutagenesis, 2014, 29 (5) : 303 - 310.
  • 2HEAD S R, KIYOMI K H, LAMERE S A, et al. Library construction for next-generation sequencing: overviews and challenges [ J ]. Biotechniques, 2014, 56 (2) : 61 - 77.
  • 3LIU L, LI Y H, LI S L, et al. Comparison of next-gener- ation sequencing systems[ J]. Journal of Biomedicine and Bioteehnology, 2012,2012: Art 251364,7pp.
  • 4HENGEN P N. Shearing DNA for genomic library con- struction[J]. Trends in Biochemical Sciences, 1997, 22 (7) :273 -276.
  • 5MANNEVILLE S, CLUZEL P, VIOVY J L, et al. Evi- dence for the universal scaling behaviour of a freely rela- xing DNA molecule [ Jl. Europhysics Letters, 1996, 36 (6) :413 -418.
  • 6HOHEISEL J D, NIZETIC D, LEHRACH H. Control of partial digestion combining the enzymes dam methylase and MboI [ J ]. Nucleic Acids Research, 1989, 17 (23) :9571 -9582.
  • 7KASOJI S K, PATI'ENDEN S G, MALC E P, et al. Cavitation enhancing nanodroplets mediate efficient DNA fragmentation in a bench top ultrasonic water bath [ J ]. Plos One, 2015, 10(7) : Art 0133014,15pp.
  • 8TSENG Q, LOMONOSOV A M, FURLONG E E, et al. Fragmentation of DNA in a sub-microliter microfluidic sonication device[J]. Lab on A Chip, 2012, 12(22) : 4677 - 4682.
  • 9LENTZ Y K, WORDEN L R, ANCHORDOQUY T J, et al. Effect of jet nebulization on DNA: identifying the dominant degradation mechanism and mitigation methods [ J ]. Journal of Aerosol Science, 2005, 36 (8) : 973 - 990.
  • 10SAMBROOK J, RUSSELL D W. Fragmentation of DNA by nebulization [ J ]. Cold Spring Harbor Protocols, 2006, 2006(4) :1 -3.

二级参考文献19

  • 1DiMauro S, Moraes CT. Mitochondrial encephalomyopathies. Arch Neurol, 1993, 50(11): 1197-1208.
  • 2Dimauro S, Tay S, Mancuso M. Mitochondrial encephalomyopathies: diagnostic approach. Ann N Y Acad Sci, 2004, 1011: 217-231.
  • 3DiMauro S, Schon EA. Mitochondrial respiratory-chain diseases. N Engl J Med, 2003, 348(26): 2656-2668.
  • 4Brandon MC, Lott MT, Nguyen KC, Spolim S, Navathe SB, Baldi P, Wallace DC. MITOMAP: a human mitochondrial genome database-2004 update. Nucleic Acids Res, 2005, 33(Database issue): D611-613.
  • 5Campos Y, Martin MA, Lorenzo G, Aparicio M, Cabello A, Arenas J. Sporadic MERRF/MELAS overlap syndrome associated with the 3243 tRNA(Leu(UUR)) mutation of mitochondrial DNA. Muscle Nerve, 1996, 19(2): 187-190.
  • 6Zeviani M, Muntoni F, Savarese N, Serra G, Tiranti V, Carrara F, Mariotti C, DiDonato S. A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene. Eur J Hum Genet, 1993, 1(1): 80-87.
  • 7Melone MA, Tessa A, Petrini S, Lus G, Sampaolo S, di Fede G, Santorelli FM, Cotrufo R. Revelation of a new mitoehondrial DNA mutation (G12147A) in a MELAS/ MERFF phenotype. Arch Neurol, 2004, 61(2): 269-272.
  • 8Munnich A, Rustin P. Clinical spectrum and diagnosis of mitochondrial disorders. Am J Med Genet, 2001, 106(1): 4-17.
  • 9Andrews RM, Kubacka I, Chinnery PF, Lightowlers RN, Turnbull DM, Howell N. Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA. Nat Genet, 1999, 23(2): 147.
  • 10Du W, Marsac C, Kruschina M, Ortigao F, Florentz C. Functionalized self-assembled monolayer on gold for detection of human mitochondrial tRNA gene mutations. Anal Biochem, 2003, 322(1): 14-25.

共引文献1

同被引文献3

引证文献1

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部