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DESIGN OF SEQUENCING PRIMERS AND PCR-BASED METHOD FOR SEQUENCING WHOLE GENOME

机译:全基因组测序的启动子设计和基于PCR的方法

摘要

Disclosed are a sequencing primer set, comprising a universal upstream primer, a universal downstream primer, and a promoter-enriched downstream primer; and a PCR-based method for sequencing a whole genome, the method comprising: by using the universal upstream primer and the universal downstream primer, performing first PCR amplification on the DNA of a sample to be sequenced, so as to obtain a first amplification product, and by using the universal upstream primer and the universal downstream primer, performing second PCR amplification on the DNA of the sample to be sequenced, so as to obtain a second amplification product; and simultaneously performing sequencing on the two amplification products. According to the above-mentioned method, the genome size and the sample amount can be adjustable, and the requirements for DNA quality are not high; there is no need for known SNP markers and for pre-construction of chips; and the method can meet requirements for the detection and screening of the whole genome.
机译:公开了一种测序引物组,其包括通用上游引物,通用下游引物和富含启动子的下游引物。一种基于PCR的全基因组测序方法,所述方法包括:通过使用所述通用上游引物和所述通用下游引物,对待测序样品的DNA进行第一PCR扩增,得到第一扩增产物。通过通用上游引物和通用下游引物对待测序样品的DNA进行第二次PCR扩增,得到第二个扩增产物。同时对两个扩增产物进行测序。根据上述方法,基因组大小和样品量可调节,对DNA质量的要求不高。不需要已知的SNP标记和芯片的预构建;该方法可以满足全基因组的检测和筛选要求。

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