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稳健长链SAGE(RL-SAGE):一种用于高通量转录组分析的改进型长链SAGE方法。

Robust-LongSAGE (RL-SAGE): an improved LongSAGE method for high-throughput transcriptome analysis.

作者信息

Gowda Malali, Wang Guo-Liang

机构信息

Ohio State University, Columbus, Ohio, USA.

出版信息

Methods Mol Biol. 2008;387:25-38. doi: 10.1007/978-1-59745-454-4_2.

Abstract

Serial analysis of gene expression (SAGE) is a powerful technique for large-scale transcriptome analysis in eukaryotes. However, technical difficulties in the SAGE library construction, such as low concatemer cloning efficiency, small concatemer size, and a high level of empty clones, has prohibited its widespread use as a routine technique for expression profiling in many laboratories. We recently improved the LongSAGE library construction method considerably and developed a modified version called Robust-LongSAGE, or RL-SAGE. In RL-SAGE, concatemer cloning efficiency and clone insert size were increased significantly. About 20 PCR reactions are sufficient to make a library with more than 150,000 clones. Using RL-SAGE, we have made 10 libraries of rice, maize, and the rice blast fungus Magnaporthe grisea.

摘要

基因表达序列分析(SAGE)是一种用于真核生物大规模转录组分析的强大技术。然而,SAGE文库构建中的技术难题,如低串联体克隆效率、小串联体大小和高比例的空克隆,阻碍了它在许多实验室作为表达谱常规技术的广泛应用。我们最近大幅改进了LongSAGE文库构建方法,并开发了一个改良版本,称为稳健LongSAGE(Robust-LongSAGE,或RL-SAGE)。在RL-SAGE中,串联体克隆效率和克隆插入片段大小显著提高。大约20次PCR反应就足以构建一个包含超过150,000个克隆的文库。利用RL-SAGE,我们已经构建了水稻、玉米和稻瘟病菌稻瘟菌的10个文库。

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