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Designing RNA secondary structures in coding regions

  • Stony Brook University

Research output: Chapter in Book/Report/Conference proceedingConference contributionpeer-review

1 Scopus citations

Abstract

Sophisticated regulatory structures appear within highly-constrained coding regions of genes. We study the extent to which such structures can be constructed. Can such stem loops appear essentially anywhere within coding regions, or is the potential restricted to rare amino acid sequences? While predicting secondary structures of an RNA sequence is an extensively studied problem in computational biology, the inverse problem, designing sequences based on a known structure is also important. We work on a particular version of the inverse RNA folding problem, where our goal is to achieve a targeted energy level. For a particular RNA structure, we design sequences with the maximum and minimum folding energy while maintaining desired codon distribution. Our major contributions in work is to optimize RNA secondary structure under codon constraints via fast estimation of folding energies following local modification.

Original languageEnglish
Title of host publicationBioinformatics Research and Applications - 8th International Symposium, ISBRA 2012, Proceedings
Pages299-314
Number of pages16
DOIs
StatePublished - 2012
Event8th International Symposium on Bioinformatics Research and Applications, ISBRA 2012 - Dallas, TX, United States
Duration: May 21 2012May 23 2012

Publication series

NameLecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics)
Volume7292 LNBI
ISSN (Print)0302-9743
ISSN (Electronic)1611-3349

Conference

Conference8th International Symposium on Bioinformatics Research and Applications, ISBRA 2012
Country/TerritoryUnited States
CityDallas, TX
Period05/21/1205/23/12

Keywords

  • inverse RNA folding
  • RNA structure prediction
  • Synthetic biology

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