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RNAspa: a shortest path approach for comparative prediction of the secondary structure of ncRNA molecules.

RNAspa: a shortest path approach for comparative prediction of the secondary structure of ncRNA molecules. Research Abstract Details 

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  • RNAspa: a shortest path approach for comparative prediction of the secondary structure of ncRNA molecules. Abstract Text:

    yair horeshYair Horesh,tirza donigerTirza Doniger,shulamit michaeliShulamit Michaeli,ron ungerRon Unger,yair horeshYair Horesh,tirza donigerTirza Doniger,shulamit michaeliShulamit Michaeli,ron ungerRon Unger,yair horeshYair Horesh,tirza donigerTirza Doniger,shulamit michaeliShulamit Michaeli,ron ungerRon Unger,yair horeshYair Horesh,tirza donigerTirza Doniger,shulamit michaeliShulamit Michaeli,ron ungerRon Unger,

    ABSTRACT: BACKGROUND: In recent years, RNA molecules that are not translated into proteins (ncRNAs) have drawn a great deal of attention, as they were shown to be involved in many cellular functions. One of the most important computational problems regarding ncRNA is to predict the secondary structure of a molecule from its sequence. In particular, we attempted to predict the secondary structure for a set of unaligned ncRNA molecules that are taken from the same family, and thus presumably have a similar structure. RESULTS: We developed the RNAspa program, which comparatively predicts the secondary structure for a set of ncRNA molecules in linear time in the number of molecules. We observed that in a list of several hundred suboptimal minimal free energy (MFE) predictions, as provided by the RNAsubopt program of the Vienna package, it is likely that at least one suggested structure would be similar to the true, correct one. The suboptimal solutions of each molecule are represented as a layer of vertices in a graph. The shortest path in this graph is the basis for structural predictions for the molecule. We also show that RNA secondary structures can be compared very rapidly by a simple string Edit-Distance algorithm with a minimal loss of accuracy. We show that this approach allows us to more deeply explore the suboptimal structure space. CONCLUSION: The algorithm was tested on three datasets which include several ncRNA families taken from the Rfam database. These datasets allowed for comparison of the algorithm with other methods. In these tests, RNAspa performed better than four other programs.

    RNAspa: a shortest path approach for comparative prediction of the secondary structure of ncRNA molecules. Publishing Authors By Initials

    y horeshY Horesh,t donigerT Doniger,s michaeliS Michaeli,r ungerR Unger,y horeshY Horesh,t donigerT Doniger,s michaeliS Michaeli,r ungerR Unger,y horeshY Horesh,t donigerT Doniger,s michaeliS Michaeli,r ungerR Unger,y horeshY Horesh,t donigerT Doniger,s michaeliS Michaeli,r ungerR Unger,

    For similar abstracts research abstracts see: abstracts research

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    RNAspa: a shortest path approach for comparative prediction of the secondary structure of ncRNA molecules. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: BMC bioinformatics

    VOLUME: 8

    Page Numbers: 366

    Journal Abbreviation: BMC Bioinformatics

    ISSN: 1471-2105

    DAY: 1

    MONTH: 10

    YEAR: 2007

    RNAspa: a shortest path approach for comparative prediction of the secondary structure of ncRNA molecules. Information

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    LANGUAGE: eng

    NlmUniqueID: 100965194

    RNAspa: a shortest path approach for comparative prediction of the secondary structure of ncRNA molecules. Keywords Mesh Terms:

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    Grant and Affiliation Information for RNAspa: a shortest path approach for comparative prediction of the secondary structure of ncRNA molecules.

    AFFILIATION: The Mina & Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan 52900, Israel. ron@biomodel.os.biu.ac.il.

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: BMC Bioinformatics

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