难以测序的人全长cDNA克隆的分类和鉴定

IF 0.4 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Akihiko Kishimoto, Yukio Ono, K. Murakawa, T. Ishibashi, A. Wakamatsu, K. Kanehori, N. Nomura, T. Isogai, M. Yohda, S. Sugano
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引用次数: 0

摘要

在人类全长cDNA测序项目中,共测序了30160个cDNA。其中,本课题组对3588个cdna进行了测序,主要采用引物行走法。以Phrap评分大于30为标准对两条链进行测序,序列的平均Phrap评分为76,即预期序列准确率的平均值为99.9999975%。尽管具有极高的序列可靠性,但我们在测序52个被称为不可破译的cdna时遇到了困难。长重复的cdna被认为是测序困难的可能来源;未采用随机法,引物行走法测序的最大重复长度为530 bp, 81%的长重复序列保留在orf中。在单重复区域,插入/删除率比通常区域大得多。cdna中SINE/Alu重复序列的比例为5.4%,为人类基因组重复序列的一半。在不可解读的cdna中,SINE/Alu的比例高达10%,与人类基因组的水平相同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Classification and characterization of human full-length cDNA clones that are difficult to sequence
In the Full-length Human cDNA Sequencing Project, 30,160 cDNA were sequenced. Among them, our group performed sequencing of 3,588 cDNAs, mainly using the primer walking method. The sequences achieved an average Phrap score of 76, which means the average of expected sequence accuracy was 99.9999975%, by sequencing of both strands with the criterion of a Phrap score over 30. In spite of the extremely high sequence reliability, we met with difficulty in sequencing 52 cDNAs, which are termed undecipherable cDNAs. cDNAs of long repeats were considered as a possible source of sequencing difficulty; their maximum repeat length sequenced by the primer walking method was 530 bp, without using the random method, and 81% of long repeat sequences remained in the ORFs. In single repeat regions, the insertion/deletion rates were much larger than in the usual regions. The fraction of SINE/Alu repeats in the cDNAs was 5.4%, half of the fraction of the human genome. The fraction of SINE/Alu in undecipherable cDNAs was up to 10%, the same level of the human genome.
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来源期刊
Chem-Bio Informatics Journal
Chem-Bio Informatics Journal BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
0.60
自引率
0.00%
发文量
8
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