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TWO-PRIMER SEQUENCING FOR HIGH-THROUGHPUT EXPRESSION ANALYSIS

机译:高通量表达分析的二元序列分析

摘要

The disclosure provides a method of sequencing a nucleic acid molecule that contains two or more target regions to be sequenced (such as, for example, barcodes). The invention is advantageous for sequencing by synthesis two or more target regions whose combined lengths plus the length of any intermediate sequence exceeds the available read length on a given sequencing platform. The methods of the invention utilize nucleic acid constructs containing at least the following elements: a complement of a first universal primer, a first target sequence, an optional polynucleotide spacer, a complement of a second universal primer, and a second target sequence. A first round of sequencing by synthesis is performed to sequence the first target sequence by elongating the first universal primer. Once the sequence of the first target region is obtained, and before the complement of the second primer is reached, the first round of sequencing is terminated. Thereafter, a second round of sequencing by synthesis is initiated--this time, by elongating the second universal primer, thereby sequencing the second target region.
机译:本公开内容提供了一种对包含两个或更多个待测序靶区域(例如,条形码)的核酸分子进行测序的方法。本发明对于通过合成两个或更多个靶区域的测序是有利的,所述两个或更多个靶区域的组合长度加上任何中间序列的长度超过了给定测序平台上的可用读取长度。本发明的方法利用至少包含以下元件的核酸构建体:第一通用引物的互补序列,第一靶序列,任选的多核苷酸间隔子,第二通用引物的互补序列和第二靶序列。进行第一轮合成测序,以通过延伸第一通用引物来测序第一靶序列。一旦获得了第一靶区域的序列,并且在达到第二引物的互补序列之前,终止第一轮测序。此后,开始第二轮合成测序-这次,通过延长第二个通用引物,从而对第二个目标区域进行了测序。

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