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Mini-Workshop "Models for DNA and RNA structure analysis"


Place: Bielefeld University, M3-115
Date: June 2, 2014

Guests

Aida Ouangraoua INRIA - Lille and LIFL, Université Lille 1, France
Stefan Janssen Practical Computer Science, Faculty of Technology, Bielefeld University, Germany
Marília Braga Bioinformatics research group, Inmetro, Rio de Janeiro, Brazil

Timetable

13h Aida Ouangraoua A multi-dimensional dynamic programming algorithm for aligning arc-annotated sequences
14h Stefan Janssen Kisses, ambivalent models and more: Contributions to the analysis of RNA secondary structure
15h Marília Braga The DCJ-indel model and its potential to improve homology assignment

Abstracts

Aida Ouangraoua: A multi-dimensional dynamic programming algorithm for aligning arc-annotated sequences

An arc-annotated sequence is a sequence, over a given alphabet, with additional structure described by a set of arcs joining pairs of positions in the sequence. Arc-annotated sequences have been widely used and studied for the representation and the comparison of RNA structures.

In (Jiang et al. 2002) a general edit distance model dedicated to arc-annotated sequences was introduced to account for both classical sequences edit operations and structural edit operations on arcs. Later in (Blin et al. 2007) it was shown that under this model, the general edit distance problem was NP-hard. Next in (Blin-Touzet 2006, Blin et al. 2010), a hierarchy of arc-annotated sequence alignment problems that highlights less general, but tractable, problems was introduced.

In this presentation, a refinement of this hierarchy of alignment problems and an extention of the class of tractable alignment problems are presented. A multi-dimensional dynamic programming algorithm is proposed to solve the most general problem of the hierarchy known to be tractable in the general edit distance model.

Stefan Janssen: Kisses, ambivalent models and more: Contributions to the analysis of RNA secondary structure

The full functional role of RNA in all domains of life is yet to be explored. Deep sequencing technologies generate massive data about RNA transcripts with functional potential. To decipher this information, bioinformatics methods for structural analysis are in demand. We demonstrate how to improve current secondary structure prediction in different respects.

Marília Braga: The DCJ-indel model and its potential to improve homology assignment

t.b.a.

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