首页> 外国专利> METHOD FOR USING WHOLE GENOME RE-SEQUENCING DATA TO QUICKLY IDENTIFY TRANSGENIC OR GENE EDITING MATERIAL AND INSERTION SITES THEREOF

METHOD FOR USING WHOLE GENOME RE-SEQUENCING DATA TO QUICKLY IDENTIFY TRANSGENIC OR GENE EDITING MATERIAL AND INSERTION SITES THEREOF

机译:使用全基因组重新测序数据以快速识别转基因或基因编辑材料及其插入部位的方法

摘要

Provided is a method for using whole genome re-sequencing data to quickly identify transgenic or gene editing material and insertion sites thereof, said method comprising: extracting genomic DNA; obtaining paired-end sequencing data of a whole genome; determining whether the sequence of an expression vector containing a T-DNA sequence, inserted in a plant to be sequenced, is known; determining whether there is a transgenic event or a gene editing event in the plant to be sequenced, and whether a backbone sequence transfer event has occurred; determining the insertion site of the T-DNA sequence; the method combines bioinformatic analysis means, and if an expression vector is known or unknown, it is determined whether a transgenic or gene editing event has occurred; if the expression vector is known, then not only can the precise location, direction, copy number, and flanking sequence information of the target sequence inserted into the genome be quickly and accurately given, but it is also determined whether there is a backbone sequence which is a sequence other than the target sequence inserted into the genome, and the same positioning is also provided.
机译:提供了一种使用全基因组重新测序数据以快速识别转基因或基因编辑材料及其插入位点的方法,所述方法包括:提取基因组DNA;获得全基因组的配对结束测序数据;确定是否已知在待测序的植物中插入含有T-DNA序列的表达载体的表达载体的序列。确定是否存在待测序植物中的转基因事件或基因编辑事件,以及是否发生了骨干序列转移事件;确定T-DNA序列的插入位点;该方法结合了生物信息分析装置,如果已知或未知表达载体,则确定是否已经发生转基因或基因编辑事件;如果已知表达载体,则不仅可以快速准确地提供插入到基因组中的目标序列的精确位置,方向,拷贝数和侧翼信息,但也确定是否存在骨干序列是插入到基因组中的目标序列以外的序列,并且还提供了相同的定位。

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