|Title||Highly specific and accurate selection of siRNAs for high-throughput functional assays|
|Publication Type||Journal Article|
|Year of Publication||2005|
|Authors||Santoyo, J, Vaquerizas, JM, Dopazo, J|
|Keywords||*Algorithms Base Sequence *Gene Silencing Molecular Sequence Data RNA; RNA/*methods *Software *User-Computer Interface; Small Interfering/*genetics Sequence Alignment/*methods Sequence Analysis|
MOTIVATION: Small interfering RNA (siRNA) is widely used in functional genomics to silence genes by decreasing their expression to study the resulting phenotypes. The possibility of performing large-scale functional assays by gene silencing accentuates the necessity of a software capable of the high-throughput design of highly specific siRNA. The main objective sought was the design of a large number of siRNAs with appropriate thermodynamic properties and, especially, high specificity. Since all the available procedures require, to some extent, manual processing of the results to guarantee specific results, specificity constitutes to date, the major obstacle to the complete automation of all the steps necessary for the selection of optimal candidate siRNAs. RESULT: Here, we present a program that for the first time completely automates the search for siRNAs. In SiDE, the most complete set of rules for the selection of siRNA candidates (including G+C content, nucleotides at determined positions, thermodynamic properties, propensity to form internal hairpins, etc.) is implemented and moreover, specificity is achieved by a conceptually new method. After selecting possible siRNA candidates with the optimal functional properties, putative unspecific matches, which can cause cross-hybridization, are checked in databases containing a unique entry for each gene. These truly non-redundant databases are constructed from the genome annotations (Ensembl). Also intron/exon boundaries, presence of polymorphisms (single nucleotide polymorphisms) specificity for either gene or transcript, and other features can be selected to be considered in the design of siRNAs. AVAILABILITY: The program is available as a web server at http://side.bioinfo.cnio.es. The program was written under the GPL license. CONTACT: firstname.lastname@example.org.
Santoyo, Javier Vaquerizas, Juan M Dopazo, Joaquin Comparative Study Evaluation Studies Research Support, Non-U.S. Gov’t England Bioinformatics (Oxford, England) Bioinformatics. 2005 Apr 15;21(8):1376-82. Epub 2004 Dec 10.