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5’-Cap Selection Methods and Their Application in Full-Length cDNA Library Construction and Transcription Start Site Profiling
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作者 白玲 王琪 +3 位作者 李红梅 程酩 张宁波 李华 《Journal of Shanghai Jiaotong university(Science)》 EI 2014年第5期580-586,共7页
With the accomplishment of the genome draft sequences, identification of functional elements in genome has become an urgent task. Full-length cDNAs provide an important resource for gene identification and their preci... With the accomplishment of the genome draft sequences, identification of functional elements in genome has become an urgent task. Full-length cDNAs provide an important resource for gene identification and their precise structural feature determination. It also provides a basis for genomic element definition. As many regulatory elements are around transcription start sites(TSSs), precise localization of TSSs in the genome becomes a critical step for identifying the associated core promoters. Massive parallel snapshot of TSSs at a particular time under a specific experimental condition makes it possible to globally analyze important regulatory elements around TSSs and further construct transcriptional regulatory networks. In this paper, we first reviewed two important full-length cDNA cloning techniques: cap-trapper technique and oligo-capping technique. Then,we introduced deepCAGE, a cap-trapper and deep sequencing-based TSS profiling technique, and its applications in the research of transcriptional regulation. 展开更多
关键词 cap-trapper oligo-capping deepcage transcription start sites(TSSs) deep sequencing
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