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GENE IDENTIFICATION SIGNATURE(GIS) ANALYSIS FOR TRANSCRIPT MAPPING

机译:转录映射的基因识别签名(GIS)分析

摘要

A transcript mapping method according to an embodiment of the invention is described hereinafter and combines short tag based (SAGE and MPSS) efficiency with the accuracy of full-length cDNA (flcDNA) for comprehensive characterization of transcriptomes. This method is also referred to as Gene Identification Signature (GIS) analysis. In this method, the 5' and 3' ends of full-length cDNA clones are initially extracted into a ditag structure, with the ditag concatemers of the ditag being subsequently sequenced in an efficient manner, and finally mapped to the genome for defining the gene structure. As a GIS ditag represents the 5' and 3' ends of a transcript, it is more informative than SAGE and MPSS tags. Segment lengths between 5' and 3' tag pairs are obtainable including orientation, ordering and chromosome family for efficient transcript mapping and gene location identification. Furthermore, a compressed suffix array (CSA) is used for indexing the genome sequence for improve mapping speed and to reduce computational memory requirements.
机译:在下文中描述根据本发明的实施方案的转录物作图方法,其将基于短标签的(SAGE和MPSS)效率与全长cDNA(flcDNA)的准确性相结合,以全面表征转录组。此方法也称为基因识别签名(GIS)分析。在这种方法中,全长cDNA克隆的5'和3'末端首先被提取成双标签结构,随后以有效方式对双标签的双标签连接体进行测序,最后定位到基因组中以定义基因结构体。由于GIS ditag代表成绩单的5'和3'末端,因此它比SAGE和MPSS标签更具信息性。可获得5'和3'标签对之间的片段长度,包括方向,顺序和染色体家族,以实现有效的转录本作图和基因位置识别。此外,压缩后缀数组(CSA)用于索引基因组序列,以提高定位速度并减少计算内存需求。

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