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        <identifier>oai:drops-oai.dagstuhl.de:20663</identifier>
        <datestamp>2024-11-27T23:18:03Z</datestamp>
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          <dc:title>RNA Inverse Folding Can Be Solved in Linear Time for Structures Without Isolated Stacks or Base Pairs</dc:title>
          <dc:creator>Boury, Théo</dc:creator>
          <dc:creator>Bulteau, Laurent</dc:creator>
          <dc:creator>Ponty, Yann</dc:creator>
          <dc:subject>RNA structure</dc:subject>
          <dc:subject>String Design</dc:subject>
          <dc:subject>Parameterized Complexity</dc:subject>
          <dc:subject>Uniform Sampling</dc:subject>
          <dc:description>Inverse folding is a classic instance of negative RNA design which consists in finding a sequence that uniquely folds into a target secondary structure with respect to energy minimization. A breakthrough result of Bonnet et al. shows that, even in simple base pairs-based (BP) models, the decision version of a mildly constrained version of inverse folding is NP-hard. &#13;
In this work, we show that inverse folding can be solved in linear time for a large collection of targets, including every structure that contains no isolated BP and no isolated stack (or, equivalently, when all helices consist of 3^{+} base pairs). For structures featuring shorter helices, our linear algorithm is no longer guaranteed to produce a solution, but still does so for a large proportion of instances.&#13;
Our approach introduces a notion of modulo m-separability, generalizing a property pioneered by Hales et al. Separability is a sufficient condition for the existence of a solution to the inverse folding problem. We show that, for any input secondary structure of length n, a modulo m-separated sequence can be produced in time 𝒪(n 2^m) anytime such a sequence exists. Meanwhile, we show that any structure consisting of 3^{+} base pairs is either trivially non-designable, or always admits a modulo-2 separated solution (m = 2). Solution sequences can thus be produced in linear time, and even be uniformly generated within the set of modulo-2 separable sequences.</dc:description>
          <dc:publisher>Schloss Dagstuhl – Leibniz-Zentrum für Informatik</dc:publisher>
          <dc:contributor>Théo Boury and Laurent Bulteau and Yann Ponty</dc:contributor>
          <dc:date>2024</dc:date>
          <dc:relation>Is Part Of LIPIcs, Volume 312, 24th International Workshop on Algorithms in Bioinformatics (WABI 2024)</dc:relation>
          <dc:type>InProceedings</dc:type>
          <dc:type>Text</dc:type>
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          <dc:identifier>doi:10.4230/LIPIcs.WABI.2024.19</dc:identifier>
          <dc:identifier>urn:nbn:de:0030-drops-206632</dc:identifier>
          <dc:identifier>https://drops.dagstuhl.de/entities/document/10.4230/LIPIcs.WABI.2024.19</dc:identifier>
          <dc:language>eng</dc:language>
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