首页> 外国专利> METHOD AND KIT FOR DETERMINING THE GENOME INTEGRITY AND/OR THE QUALITY OF A LIBRARY OF DNA SEQUENCES OBTAINED BY DETERMINISTIC RESTRICTION SITE WHOLE GENOME AMPLIFICATION

METHOD AND KIT FOR DETERMINING THE GENOME INTEGRITY AND/OR THE QUALITY OF A LIBRARY OF DNA SEQUENCES OBTAINED BY DETERMINISTIC RESTRICTION SITE WHOLE GENOME AMPLIFICATION

机译:确定性限制位点全基因组扩增获得的DNA序列的基因组完整性和/或质量的方法和试剂盒

摘要

A method for determining the integrity of the genome of a sample and/or the quality of a library of DNA sequences obtained by deterministic restriction site whole genome amplification can include (a) amplifying the library of DNA sequences to produce first, second, and third PCR products each of a different size from 50 bp to 1000 bp, by PCR using at least one first primer pair, one second primer pair and one third primer pair, the primer pairs each hybridizing to a DNA sequence of the library having a length from 1000 bp to 5000 bp and corresponding to a sequence of the genome located respectively on a first, second and third chromosome arm; (b) detecting the first, second and third PCR products; (c) correlating the presence of the first, second and third PCR products with the integrity of the genome of the sample and/or the quality of the library.
机译:用于确定样品基因组完整性和/或通过确定性限制性位点进行全基因组扩增而获得的DNA序列文库质量的方法可包括(a)扩增DNA序列文库以产生第一,第二和第三种通过使用至少一个第一引物对,一个第二引物对和一个第三引物对进行PCR,将PCR产物的大小从50 bp改变为1000 bp,每个引物对与文库的DNA序列杂交,长度分别为1000bp至5000bp,对应于分别位于第一,第二和第三染色体臂上的基因组序列; (b)检测第一,第二和第三PCR产物; (c)将第一,第二和第三PCR产物的存在与样品基因组的完整性和/或文库的质量相关联。

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