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本文引用的文献

1
ESTprep: preprocessing cDNA sequence reads.ESTprep:预处理cDNA序列读数。
Bioinformatics. 2003 Jul 22;19(11):1318-24. doi: 10.1093/bioinformatics/btg159.
2
Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.超过15000条全长人类和小鼠cDNA序列的生成与初步分析。
Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. doi: 10.1073/pnas.242603899. Epub 2002 Dec 11.
3
Pooled library tissue tags for EST-based gene discovery.用于基于EST的基因发现的混合文库组织标签。
Bioinformatics. 2002 Sep;18(9):1162-6. doi: 10.1093/bioinformatics/18.9.1162.
4
The Drosophila gene collection: identification of putative full-length cDNAs for 70% of D. melanogaster genes.果蝇基因文库:鉴定出约70%的黑腹果蝇基因的假定全长cDNA。
Genome Res. 2002 Aug;12(8):1294-300. doi: 10.1101/gr.269102.
5
Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome.鉴定出与巴德-比德尔综合征(一种复杂的人类肥胖综合征)最常相关的基因(BBS1)。
Nat Genet. 2002 Aug;31(4):435-8. doi: 10.1038/ng935. Epub 2002 Jul 15.
6
Annotated expressed sequence tags and cDNA microarrays for studies of brain and behavior in the honey bee.用于蜜蜂大脑与行为研究的注释表达序列标签和cDNA微阵列。
Genome Res. 2002 Apr;12(4):555-66. doi: 10.1101/gr.5302.
7
The NIEHS Xenopus maternal EST project: interim analysis of the first 13,879 ESTs from unfertilized eggs.美国国家环境健康科学研究所非洲爪蟾母体EST项目:对来自未受精卵的首批13,879个ESTs的中期分析。
Gene. 2001 Apr 4;267(1):71-87. doi: 10.1016/s0378-1119(01)00383-3.
8
Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2).位于16号染色体上导致巴德-比德尔综合征(BBS2)的一个新基因的定位克隆。
Hum Mol Genet. 2001 Apr 1;10(8):865-74. doi: 10.1093/hmg/10.8.865.
9
An assessment of gene prediction accuracy in large DNA sequences.大型DNA序列中基因预测准确性的评估。
Genome Res. 2000 Oct;10(10):1631-42. doi: 10.1101/gr.122800.
10
Patterns of variant polyadenylation signal usage in human genes.人类基因中可变聚腺苷酸化信号使用模式。
Genome Res. 2000 Jul;10(7):1001-10. doi: 10.1101/gr.10.7.1001.

大鼠中的高通量基因发现

High-throughput gene discovery in the rat.

作者信息

Scheetz Todd E, Laffin Jennifer J, Berger Brian, Holte Sara, Baumes Susan A, Brown Robert, Chang Shereen, Coco Justin, Conklin Jim, Crouch Keith, Donohue Micca, Doonan Greg, Estes Chris, Eyestone Mari, Fishler Katrina, Gardiner Jack, Guo Lankai, Johnson Brad, Keppel Catherine, Kreger Rikki, Lebeck Mark, Marcelino Rudy, Miljkovich Vladan, Perdue Mindee, Qui Ling, Rehmann Joshua, Reiter Rebecca S, Rhoads Bridgette, Schaefer Kelly, Smith Christina, Sunjevaric Ivana, Trout Kurtis, Wu Ning, Birkett Clayton L, Bischof Jared, Gackle Barry, Gavin Allen, Grundstad A Jason, Mokrzycki Brian, Moressi Chris, O'Leary Brian, Pedretti Kevin, Roberts Chad, Robinson Natalie L, Smith Michael, Tack Dylan, Trivedi Nishank, Kucaba Tamara, Freeman Tom, Lin Jim J-C, Bonaldo Maria F, Casavant Thomas L, Sheffield Val C, Soares M Bento

机构信息

Center for Bioinformatics and Computational Biology, The University of Iowa, Iowa City, Iowa 52242, USA.

出版信息

Genome Res. 2004 Apr;14(4):733-41. doi: 10.1101/gr.1414204.

DOI:10.1101/gr.1414204
PMID:15060017
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC383320/
Abstract

The rat is an important animal model for human diseases and is widely used in physiology. In this article we present a new strategy for gene discovery based on the production of ESTs from serially subtracted and normalized cDNA libraries, and we describe its application for the development of a comprehensive nonredundant collection of rat ESTs. Our new strategy appears to yield substantially more EST clusters per ESTs sequenced than do previous approaches that did not use serial subtraction. However, multiple rounds of library subtraction resulted in high frequencies of otherwise rare internally primed cDNAs, defining the limits of this powerful approach. To date, we have generated >200,000 3' ESTs from >100 cDNA libraries representing a wide range of tissues and developmental stages of the laboratory rat. Most importantly, we have contributed to approximately 50,000 rat UniGene clusters. We have identified, arrayed, and derived 5' ESTs from >30,000 unique rat cDNA clones. Complete information, including radiation hybrid mapping data, is also maintained locally at http://genome.uiowa.edu/clcg.html. All of the sequences described in this article have been submitted to the dbEST division of the NCBI.

摘要

大鼠是人类疾病的重要动物模型,在生理学研究中被广泛应用。在本文中,我们提出了一种基于从连续扣除和标准化的cDNA文库中产生ESTs来进行基因发现的新策略,并描述了其在构建大鼠ESTs全面非冗余集合中的应用。我们的新策略似乎比以前未使用连续扣除的方法在每个测序的EST中产生更多的EST簇。然而,多轮文库扣除导致原本罕见的内部引物cDNA出现高频,这界定了这种强大方法的局限性。迄今为止,我们已经从代表实验大鼠广泛组织和发育阶段的100多个cDNA文库中产生了超过200,000个3' ESTs。最重要的是,我们为大约50,000个大鼠单基因簇做出了贡献。我们已经从超过30,000个独特的大鼠cDNA克隆中鉴定、排列并获得了5' ESTs。完整信息,包括辐射杂种图谱数据,也保存在本地网站http://genome.uiowa.edu/clcg.html上。本文描述的所有序列已提交至NCBI的dbEST部门。