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IMPROVED NEXT-GENERATION SEQUENCING

机译:改进的下一代排序

摘要

The present invention enables the determination by NGS of the full nucleotide sequence of one or more polynucleotides of interest that are more than 800 bp in length after only one round of PCR amplification and subsequent fragmentation by adding at least one known oligonucleotide index to at least one end of each polynucleotide to produce elongated polynucleotides, wherein each known oligonucleotide index added to each polynucleotide is unique; fragmenting the elongated polynucleotides; sequencing the resulting fragments with paired forward and reverse reads using bridge amplification and next-generation sequencing; sorting the paired sequences based on the known oligonucleotide; and performing manual or in silico assembly of the sorted paired sequences, thereby providing the full coding sequence of each of the multitude of polynucleotides.
机译:本发明使得能够在仅一轮PCR扩增和随后的片段化之后通过将至少一种已知的寡核苷酸索引添加至至少一个,通过NGS确定长度大于800bp的一种或多种目的多核苷酸的完整核苷酸序列。每个多核苷酸的末端以产生拉长的多核苷酸,其中添加到每个多核苷酸的每个已知寡核苷酸索引是唯一的;片段化细长的多核苷酸;使用桥扩增和下一代测序,将成对的片段与成对的正向和反向读数进行测序;根据已知的寡核苷酸对配对序列进行分选;以及对分类的配对序列进行手工或计算机组装,从而提供多种多核苷酸中每一个的完整编码序列。

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