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Characterization of One-Pass and Pull-Length Sequences of Oligo-Capping cDNA Clones by Genome Mapping

机译:基因组映射对寡核封端cDNA克隆单次和拉伸长度序列的表征

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Whole human genome sequence determination was completed this year. To obtain accurate gene structures and promoter information, full-length cDNA sequence information as well as the genome sequences is indispensable. Moreover, the full-length cDNA clones and sequences are valuable for functional analysis of genes. The oligo-capping cDNA library developed by Maruyama and Sugano is an effective source of the full-length cDNA clones. The full-length human cDNA sequencing project supported by New Energy and Industrial Technology Developmental Organization (NEDO) determined 30,000 full-length and more than one million 5' one pass cDNA sequences of oligo-capping clones obtained at HRI and Tokyo University. Consequently, the NEDO human splicing variant cDNAproject started in 2002, taking advantage of these oligo-capping cDNAs which are regarded as a valuable source of splicing variant cDNAs.
机译:整个人类基因组序列测定完成今年。为了获得准确的基因结构和启动子信息,全长cDNA序列信息以及基因组序列是必不可少的。此外,全长cDNA克隆和序列对于基因的功能分析是有价值的。由Maruyama和Sugano开发的寡核 - 封盖cDNA文库是全长cDNA克隆的有效来源。新能源和工业技术发展组织(NEDO)支持的全长人类cDNA测序项目(NEDO)确定了30,000个全长,超过一百万5百万5'一键在HRI和东京大学获得的寡核封装克隆的CDNA序列。因此,NEDO人剪接变体cdnaprapt在2002年开始,利用这些寡核封端CDNA,其被认为是剪接变体CDNA的有价值的来源。

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