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本文引用的文献

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Rational siRNA design for RNA interference.用于RNA干扰的合理siRNA设计
Nat Biotechnol. 2004 Mar;22(3):326-30. doi: 10.1038/nbt936. Epub 2004 Feb 1.
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Database resources of the National Center for Biotechnology Information: update.美国国立生物技术信息中心的数据库资源:更新
Nucleic Acids Res. 2004 Jan 1;32(Database issue):D35-40. doi: 10.1093/nar/gkh073.
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Functional siRNAs and miRNAs exhibit strand bias.功能性小干扰RNA和微小RNA表现出链偏好性。
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Asymmetry in the assembly of the RNAi enzyme complex.RNA干扰酶复合体组装中的不对称性。
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Identification of modulators of TRAIL-induced apoptosis via RNAi-based phenotypic screening.通过基于RNA干扰的表型筛选鉴定TRAIL诱导凋亡的调节因子。
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Sequence, chemical, and structural variation of small interfering RNAs and short hairpin RNAs and the effect on mammalian gene silencing.小干扰RNA和短发夹RNA的序列、化学及结构变异及其对哺乳动物基因沉默的影响。
Antisense Nucleic Acid Drug Dev. 2003 Apr;13(2):83-105. doi: 10.1089/108729003321629638.
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Killing the messenger: short RNAs that silence gene expression.杀死信使:沉默基因表达的短RNA
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Mammalian RNAi for the masses.面向大众的哺乳动物RNA干扰技术。
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Analysis of gene function in somatic mammalian cells using small interfering RNAs.利用小干扰RNA分析哺乳动物体细胞中的基因功能。
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小干扰RNA选择服务器:一个自动化的小干扰RNA寡核苷酸预测服务器。

siRNA Selection Server: an automated siRNA oligonucleotide prediction server.

作者信息

Yuan Bingbing, Latek Robert, Hossbach Markus, Tuschl Thomas, Lewitter Fran

机构信息

Whitehead Institute for Biomedical Research, Bioinformatics and Research Computing, Nine Cambridge Center, Cambridge, MA 02142, USA.

出版信息

Nucleic Acids Res. 2004 Jul 1;32(Web Server issue):W130-4. doi: 10.1093/nar/gkh366.

DOI:10.1093/nar/gkh366
PMID:15215365
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC441504/
Abstract

The Whitehead siRNA (short interfering RNA) Selection Web Server (http://jura.wi.mit.edu/bioc/siRNA) automates the design of short oligonucleotides that can specifically 'knock down' expression of target genes. These short sequences are about 21 nt in length, and when synthesized as double stranded RNA and introduced into cell culture, can reduce or eliminate the function of the target gene. Depending on the length of a gene, there are potentially numerous combinations of possible 21mers. Some experimental evidence has already shown that not all 21mers in a gene have the same effectiveness at silencing gene function. Our tool incorporates published design rules and presents the scientist with information about uniqueness of the 21mers within the genome, thermodynamic stability of the double stranded RNA duplex, GC content, presence of SNPs and other features that may contribute to the effectiveness of a siRNA.

摘要

怀特黑德小干扰RNA(siRNA)筛选网络服务器(http://jura.wi.mit.edu/bioc/siRNA)可自动设计能特异性“敲低”靶基因表达的短寡核苷酸。这些短序列长度约为21个核苷酸,当合成为双链RNA并引入细胞培养物中时,可降低或消除靶基因的功能。根据基因的长度,可能存在众多21聚体的组合。一些实验证据已经表明,基因中的并非所有21聚体在沉默基因功能方面都具有相同的效力。我们的工具纳入了已发表的设计规则,并向科学家提供有关基因组内21聚体的独特性、双链RNA双链体的热力学稳定性、GC含量、单核苷酸多态性的存在以及其他可能有助于小干扰RNA有效性的特征的信息。