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High resolution analysis of point mutations by constant denaturant capillary electrophoresis (CDCE).

作者信息

Khrapko K, Coller H A, Li-Sucholeiki X C, André P C, Thilly W G

机构信息

Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, USA.

出版信息

Methods Mol Biol. 2001;163:57-72. doi: 10.1385/1-59259-116-7:57.

DOI:10.1385/1-59259-116-7:57
PMID:11242964
Abstract
摘要

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引用本文的文献

1
Analysis of mutational spectra by denaturing capillary electrophoresis.通过变性毛细管电泳分析突变谱。
Nat Protoc. 2008;3(7):1153-66. doi: 10.1038/nprot.2008.79.
2
s-RT-MELT for rapid mutation scanning using enzymatic selection and real time DNA-melting: new potential for multiplex genetic analysis.利用酶促筛选和实时DNA熔解进行快速突变扫描的s-RT-MELT：多重基因分析的新潜力。
Nucleic Acids Res. 2007;35(12):e84. doi: 10.1093/nar/gkm403. Epub 2007 Jun 1.
3
Ligation of high-melting-temperature 'clamp' sequence extends the scanning range of rare point-mutational analysis by constant denaturant capillary electrophoresis (CDCE) to most of the human genome.
高熔点“钳夹”序列的连接将恒定变性剂毛细管电泳（CDCE）的稀有点突变分析扫描范围扩展到了大部分人类基因组。
Nucleic Acids Res. 2003 Aug 15;31(16):e97. doi: 10.1093/nar/gng099.
4
DNA variants in the ATM gene are not associated with sporadic rectal cancer in a Norwegian population-based study.
Int J Colorectal Dis. 2004 Jan;19(1):49-54. doi: 10.1007/s00384-003-0519-7. Epub 2003 Jun 21.