生物
杂交测序
转座因子
结扎测序
寡核苷酸
核糖核酸
DNA
DNA纳米球测序
遗传学
DNA测序
核酸
计算生物学
分子生物学
基因组文库
基因
基因组
DNA测序器
基序列
作者
Yanjun Zhang,Yin Tang,Zhongxing Sun,Junqi Jia,Yuan Fang,Xinyi Wan,Fang Dong
出处
期刊:Genome Research
[Cold Spring Harbor Laboratory Press]
日期:2023-03-01
卷期号:33 (3): 412-426
被引量:11
标识
DOI:10.1101/gr.277213.122
摘要
Tn5 transposon tagments double-stranded DNA and RNA/DNA hybrids to generate nucleic acids that are ready to be amplified for high-throughput sequencing. The nucleic acid substrates for the Tn5 transposon must be explored to increase the applications of Tn5. Here, we found that the Tn5 transposon can transpose oligos into the 5′ end of single-stranded DNA longer than 140 nucleotides. Based on this property of Tn5, we developed a tagmentation-based and ligation-enabled single-stranded DNA sequencing method called TABLE-seq. Through a series of reaction temperature, time, and enzyme concentration tests, we applied TABLE-seq to strand-specific RNA sequencing, starting with as little as 30 pg of total RNA. Moreover, compared with traditional dUTP-based strand-specific RNA sequencing, this method detects more genes, has a higher strand specificity, and shows more evenly distributed reads across genes. Together, our results provide insights into the properties of Tn5 transposons and expand the applications of Tn5 in cutting-edge sequencing techniques.
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