Literature DB >> 11238069

The massively parallel genetic algorithm for RNA folding: MIMD implementation and population variation.

B A Shapiro1, J C Wu, D Bengali, M J Potts.   

Abstract

A massively parallel Genetic Algorithm (GA) has been applied to RNA sequence folding on three different computer architectures. The GA, an evolution-like algorithm that is applied to a large population of RNA structures based on a pool of helical stems derived from an RNA sequence, evolves this population in parallel. The algorithm was originally designed and developed for a 16384 processor SIMD (Single Instruction Multiple Data) MasPar MP-2. More recently it has been adapted to a 64 processor MIMD (Multiple Instruction Multiple Data) SGI ORIGIN 2000, and a 512 processor MIMD CRAY T3E. The MIMD version of the algorithm raises issues concerning RNA structure data-layout and processor communication. In addition, the effects of population variation on the predicted results are discussed. Also presented are the scaling properties of the algorithm from the perspective of the number of physical processors utilized and the number of virtual processors (RNA structures) operated upon.

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Year:  2001        PMID: 11238069     DOI: 10.1093/bioinformatics/17.2.137

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  21 in total

1.  Analysis of DNA microarrays using algorithms that employ rule-based expert knowledge.

Authors:  Kuang-Hung Pan; Chih-Jian Lih; Stanley N Cohen
Journal:  Proc Natl Acad Sci U S A       Date:  2002-02-19       Impact factor: 11.205

2.  Discovery of RNA structural elements using evolutionary computation.

Authors:  Gary B Fogel; V William Porto; Dana G Weekes; David B Fogel; Richard H Griffey; John A McNeil; Elena Lesnik; David J Ecker; Rangarajan Sampath
Journal:  Nucleic Acids Res       Date:  2002-12-01       Impact factor: 16.971

3.  Identification of cis-acting elements in the 3'-untranslated region of the dengue virus type 2 RNA that modulate translation and replication.

Authors:  Mark Manzano; Erin D Reichert; Stephanie Polo; Barry Falgout; Wojciech Kasprzak; Bruce A Shapiro; Radhakrishnan Padmanabhan
Journal:  J Biol Chem       Date:  2011-04-22       Impact factor: 5.157

4.  A pseudoknot in a preactive form of a viral RNA is part of a structural switch activating minus-strand synthesis.

Authors:  Jiuchun Zhang; Guohua Zhang; Rong Guo; Bruce A Shapiro; Anne E Simon
Journal:  J Virol       Date:  2006-09       Impact factor: 5.103

5.  A base-specific recognition signal in the 5' consensus sequence of rotavirus plus-strand RNAs promotes replication of the double-stranded RNA genome segments.

Authors:  M Alejandra Tortorici; Bruce A Shapiro; John T Patton
Journal:  RNA       Date:  2005-11-21       Impact factor: 4.942

6.  A heuristic approach for detecting RNA H-type pseudoknots.

Authors:  Chun-Hsiang Huang; Chin Lung Lu; Hsien-Tai Chiu
Journal:  Bioinformatics       Date:  2005-06-30       Impact factor: 6.937

7.  The role of a metastable RNA secondary structure in hepatitis delta virus genotype III RNA editing.

Authors:  Sarah D Linnstaedt; Wojciech K Kasprzak; Bruce A Shapiro; John L Casey
Journal:  RNA       Date:  2006-06-21       Impact factor: 4.942

8.  RNA secondary structure prediction from sequence alignments using a network of k-nearest neighbor classifiers.

Authors:  Eckart Bindewald; Bruce A Shapiro
Journal:  RNA       Date:  2006-03       Impact factor: 4.942

9.  The fraction of RNA that folds into the correct branched secondary structure determines hepatitis delta virus type 3 RNA editing levels.

Authors:  Sarah D Linnstaedt; Wojciech K Kasprzak; Bruce A Shapiro; John L Casey
Journal:  RNA       Date:  2009-04-21       Impact factor: 4.942

10.  RNA2D3D: a program for generating, viewing, and comparing 3-dimensional models of RNA.

Authors:  Hugo M Martinez; Jacob V Maizel; Bruce A Shapiro
Journal:  J Biomol Struct Dyn       Date:  2008-06
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