10,266 research outputs found
Comparing RNA structures using a full set of biologically relevant edit operations is intractable
7 pagesArc-annotated sequences are useful for representing structural information of RNAs and have been extensively used for comparing RNA structures in both terms of sequence and structural similarities. Among the many paradigms referring to arc-annotated sequences and RNA structures comparison (see \cite{IGMA_BliDenDul08} for more details), the most important one is the general edit distance. The problem of computing an edit distance between two non-crossing arc-annotated sequences was introduced in \cite{Evans99}. The introduced model uses edit operations that involve either single letters or pairs of letters (never considered separately) and is solvable in polynomial-time \cite{ZhangShasha:1989}. To account for other possible RNA structural evolutionary events, new edit operations, allowing to consider either silmutaneously or separately letters of a pair were introduced in \cite{jiangli}; unfortunately at the cost of computational tractability. It has been proved that comparing two RNA secondary structures using a full set of biologically relevant edit operations is {\sf\bf NP}-complete. Nevertheless, in \cite{DBLP:conf/spire/GuignonCH05}, the authors have used a strong combinatorial restriction in order to compare two RNA stem-loops with a full set of biologically relevant edit operations; which have allowed them to design a polynomial-time and space algorithm for comparing general secondary RNA structures. In this paper we will prove theoretically that comparing two RNA structures using a full set of biologically relevant edit operations cannot be done without strong combinatorial restrictions
Louse (Insecta : Phthiraptera) mitochondrial 12S rRNA secondary structure is highly variable
Lice are ectoparasitic insects hosted by birds and mammals. Mitochondrial 12S rRNA sequences obtained from lice show considerable length variation and are very difficult to align. We show that the louse 12S rRNA domain III secondary structure displays considerable variation compared to other insects, in both the shape and number of stems and loops. Phylogenetic trees constructed from tree edit distances between louse 12S rRNA structures do not closely resemble trees constructed from sequence data, suggesting that at least some of this structural variation has arisen independently in different louse lineages. Taken together with previous work on mitochondrial gene order and elevated rates of substitution in louse mitochondrial sequences, the structural variation in louse 12S rRNA confirms the highly distinctive nature of molecular evolution in these insects
Efficient chaining of seeds in ordered trees
We consider here the problem of chaining seeds in ordered trees. Seeds are
mappings between two trees Q and T and a chain is a subset of non overlapping
seeds that is consistent with respect to postfix order and ancestrality. This
problem is a natural extension of a similar problem for sequences, and has
applications in computational biology, such as mining a database of RNA
secondary structures. For the chaining problem with a set of m constant size
seeds, we describe an algorithm with complexity O(m2 log(m)) in time and O(m2)
in space
Reconstructing phylogeny from RNA secondary structure via simulated evolution
DNA sequences of genes encoding functional RNA molecules (e.g., ribosomal RNAs) are commonly used in phylogenetics (i.e. to infer evolutionary history). Trees derived from ribosomal RNA (rRNA) sequences, however, are inconsistent with other molecular data in investigations of deep branches in the tree of life. Since much of te functional constraints on the gene products (i.e. RNA molecules) relate to three-dimensional structure, rather than their actual sequences, accumulated mutations in the gene sequences may obscure phylogenetic signal over very large evolutionary time-scales. Variation in structure, however, may be suitable for phylogenetic inference even under extreme sequence divergence. To evaluate qualitatively the manner in which structural evolution relates to sequence change, we simulated the evolution of RNA sequences under various constraints on structural change
Tree decomposition and parameterized algorithms for RNA structure-sequence alignment including tertiary interactions and pseudoknots
We present a general setting for structure-sequence comparison in a large
class of RNA structures that unifies and generalizes a number of recent works
on specific families on structures. Our approach is based on tree decomposition
of structures and gives rises to a general parameterized algorithm, where the
exponential part of the complexity depends on the family of structures. For
each of the previously studied families, our algorithm has the same complexity
as the specific algorithm that had been given before.Comment: (2012
Improved Algorithms for Approximate String Matching (Extended Abstract)
The problem of approximate string matching is important in many different
areas such as computational biology, text processing and pattern recognition. A
great effort has been made to design efficient algorithms addressing several
variants of the problem, including comparison of two strings, approximate
pattern identification in a string or calculation of the longest common
subsequence that two strings share.
We designed an output sensitive algorithm solving the edit distance problem
between two strings of lengths n and m respectively in time
O((s-|n-m|)min(m,n,s)+m+n) and linear space, where s is the edit distance
between the two strings. This worst-case time bound sets the quadratic factor
of the algorithm independent of the longest string length and improves existing
theoretical bounds for this problem. The implementation of our algorithm excels
also in practice, especially in cases where the two strings compared differ
significantly in length. Source code of our algorithm is available at
http://www.cs.miami.edu/\~dimitris/edit_distanceComment: 10 page
Geometric medians in reconciliation spaces
In evolutionary biology, it is common to study how various entities evolve
together, for example, how parasites coevolve with their host, or genes with
their species. Coevolution is commonly modelled by considering certain maps or
reconciliations from one evolutionary tree to another , all of which
induce the same map between the leaf-sets of and (corresponding
to present-day associations). Recently, there has been much interest in
studying spaces of reconciliations, which arise by defining some metric on
the set of all possible reconciliations between and .
In this paper, we study the following question: How do we compute a geometric
median for a given subset of relative to , i.e. an
element such that holds for all
? For a model where so-called host-switches or
transfers are not allowed, and for a commonly used metric called the
edit-distance, we show that although the cardinality of can be
super-exponential, it is still possible to compute a geometric median for a set
in in polynomial time. We expect that this result could
be useful for computing a summary or consensus for a set of reconciliations
(e.g. for a set of suboptimal reconciliations).Comment: 12 pages, 1 figur
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