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Method and kit for determining genomic integrity and / or quality of a library of DNA sequences obtained by whole genome amplification of definitive restriction enzyme sites

机译:通过全基因组扩增确定性限制性内切酶位点确定的DNA序列文库的基因组完整性和/或质量的方法和试剂盒

摘要

The present invention comprises: (a) providing a library of DNA sequences; and (b) PGR using at least one first primer pair, one second primer pair, and one third primer pair. A step of amplifying a library of DNA sequences, wherein said primer pair has a length of 1000 bp to 5000 bp and is located in each of the first chromosomal arm, the second chromosomal arm and the third chromosomal arm; A first PCR product, a second PCR product, and a third PCR product, each of which hybridizes to the DNA sequence of the library corresponding to the sequence, and wherein the amplification step is 50 bp to 1000 bp each and has a different size from each other. (C) detecting a first PCR product, a second PCR product, and a third PCR product; and (d) a first P product. Associating the presence of the R product, the second PCR product, and the third PCR product with the genomic integrity of the sample and / or the quality of the library of DNA sequences, and It relates to a method for determining the quality of a DNA sequence library obtained by definitive restriction enzyme site whole genome amplification (DRS-WGA) of the genome of a sample. [Selection] Figure 1
机译:本发明包括:(a)提供DNA序列文库; (b)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的PGR。扩增DNA序列文库的步骤,其中所述引物对的长度为1000bp至5000bp,并且位于第一染色体臂,第二染色体臂和第三染色体臂的每一个中;第一PCR产物,第二PCR产物和第三PCR产物,其各自与对应于该序列的文库的DNA序列杂交,并且其中扩增步骤各自为50bp至1000bp,并且具有与彼此。 (C)检测第一PCR产物,第二PCR产物和第三PCR产物; (d)第一种P产品。将R产物,第二PCR产物和第三PCR产物的存在与样品的基因组完整性和/或DNA序列文库的质量相关联,并且涉及确定DNA质量的方法通过确定基因组的限制性酶切位点全基因组扩增(DRS-WGA)获得的序列文库。 [选择]图1

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