Michel Termier
University of Paris-Sud
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Featured researches published by Michel Termier.
FEBS Letters | 2000
Monique Bolotin-Fukuhara; Claire Toffano-Nioche; François Artiguenave; Guillemette Duchateau-Nguyen; Marc Lemaire; Roland Marmeisse; Robert Montrocher; Catherine Robert; Michel Termier; Patrick Wincker; Micheline Wésolowski-Louvel
Random sequencing of the Kluyveromyces lactis genome allowed the identification of 2235–2601 open reading frames (ORFs) homologous to S. cerevisiae ORFs, 51 ORFs which were homologous to genes from other species, 64 tRNAs, the complete rDNA repeat, and a few Ty1‐ and Ty2‐like sequences. In addition, the complete sequence of plasmid pKD1 and a large coverage of the mitochondrial genome were obtained. The global distribution into general functional categories found in Saccharomyces cerevisiae and as defined by MIPS is well conserved in K. lactis. However, detailed examination of certain subcategories revealed a small excess of genes involved in amino acid metabolism in K. lactis. The sequences are deposited at EMBL under the accession numbers AL424881–AL430960.
Bioinformatics | 2003
Michaël Bekaert; Laure Bidou; Alain Denise; Guillemette Duchateau-Nguyen; Jean-Paul Forest; Christine Froidevaux; Isabelle Hatin; Jean-Pierre Rousset; Michel Termier
Abstract Motivation: Unconventional decoding events are now well acknowledged, but not yet well formalized. In this study, we present a bioinformatics analysis of eukaryotic −1 frameshifting, in order to model this event. Results: A consensus model has already been established for −1 frameshifting sites. Our purpose here is to provide new constraints which make the model more precise. We show how a machine learning approach can be used to refine the current model. We identify new properties that may be involved in frameshifting. Each of the properties found was experimentally validated. Initially, we identify features of the overall model that are to be simultaneously satisfied. We then focus on the following two components: the spacer and the slippery sequence. As a main result, we point out that the identity of the primary structure of the so-called spacer is of great importance. Availability: Sequences of the oligonucleotides in the functional tests are available at http://www.igmors.u-psud.fr/rousset/bioinformatics/ Contact: [email protected]@[email protected] * To whom correspondence should be addressed.
Bioinformatics | 2006
Yann Ponty; Michel Termier; Alain Denise
SUMMARY GenRGenS is a software tool dedicated to randomly generating genomic sequences and structures. It handles several classes of models useful for sequence analysis, such as Markov chains, hidden Markov models, weighted context-free grammars, regular expressions and PROSITE expressions. GenRGenS is the only program that can handle weighted context-free grammars, thus allowing the user to model and to generate structured objects (such as RNA secondary structures) of any given desired size. GenRGenS also allows the user to combine several of these different models at the same time.
FEBS Letters | 2000
Claude Gaillardin; Guillemette Duchateau-Nguyen; Fredj Tekaia; Bertrand Llorente; Serge Casaregola; Claire Toffano-Nioche; Michel Aigle; François Artiguenave; Gaëlle Blandin; Monique Bolotin-Fukuhara; Elisabeth Bon; Jacky de Montigny; Bernard Dujon; Pascal Durrens; Andrée Lépingle; Alain Malpertuy; Cécile Neuvéglise; Odile Ozier-Kalogeropoulos; Serge Potier; William Saurin; Michel Termier; Micheline Wésolowski-Louvel; Patrick Wincker; Jean-Luc Souciet; Jean Weissenbach
We explored the biological diversity of hemiascomycetous yeasts using a set of 22 000 newly identified genes in 13 species through BLASTX searches. Genes without clear homologue in Saccharomyces cerevisiae appeared to be conserved in several species, suggesting that they were recently lost by S. cerevisiae. They often identified well‐known species‐specific traits. Cases of gene acquisition through horizontal transfer appeared to occur very rarely if at all. All identified genes were ascribed to functional classes. Functional classes were differently represented among species. Species classification by functional clustering roughly paralleled rDNA phylogeny. Unequal distribution of rapidly evolving, ascomycete‐specific, genes among species and functions was shown to contribute strongly to this clustering. A few cases of gene family amplification were documented, but no general correlation could be observed between functional differentiation of yeast species and variations of gene family sizes. Yeast biological diversity seems thus to result from limited species‐specific gene losses or duplications, and for a large part from rapid evolution of genes and regulatory factors dedicated to specific functions.
Advances in Bioinformatics | 2012
Julien Allali; Cédric Saule; Cedric Chauve; Yves d'Aubenton-Carafa; Alain Denise; Christine Drevet; Pascal Ferraro; Daniel Gautheret; Claire Herrbach; Fabrice Leclerc; Antoine de Monte; Aïda Ouangraoua; Marie-France Sagot; Michel Termier; Claude Thermes; Hélène Touzet
The pairwise comparison of RNA secondary structures is a fundamental problem, with direct application in mining databases for annotating putative noncoding RNA candidates in newly sequenced genomes. An increasing number of software tools are available for comparing RNA secondary structures, based on different models (such as ordered trees or forests, arc annotated sequences, and multilevel trees) and computational principles (edit distance, alignment). We describe here the website BRASERO that offers tools for evaluating such software tools on real and synthetic datasets.
Archive | 2000
Alain Denise; Olivier Roques; Michel Termier
Let L be a context-free language on an alphabet X={ x 1,x2,…, xk} and n a positive integer. We consider the problem of generating at random words of L with re-spect to a given distribution of the number of occurrences of the letters. We consider two alternatives of the problem. In the first one, a vector of natural numbers (n1, n2,…,nk) such that n1 + n2+… + nk = n is given, and the words must be generated uniformly among the set of words of L which contain exactly ni letters xi (1 ≤ i ≤ k). The second alternative consists, given v = (vi,…, vk) a vector of positive real numbers such that vi +… + vk = 1, to generate at random words among the whole set of words of L of length n, in such a way that the expected number of occurrences of any letter x i equals nvi (1 ≤i ≤ k), and two words having the same distribution of letters have the same probability to be generated. For this purpose, we design and study two alternatives of the recursive method which is classically employed for the uniform generation of combinatorial structures. This type of “controlled” non-uniform generation can be applied in the field of statistical analysis of genomic sequences.
Nucleic Acids Research | 2003
Olivier Namy; Guillemette Duchateau-Nguyen; Isabelle Hatin; Sylvie Hermann-Le Denmat; Michel Termier; Jean-Pierre Rousset
Theoretical Computer Science | 2010
Alain Denise; Yann Ponty; Michel Termier
research in computational molecular biology | 2003
Alain Denise; Yann Ponty; Michel Termier
Proc. JOBIM | 2007
Julien Allali; Yves d'Aubenton-Carafa; Cedric Chauve; Alain Denise; Christine Drevet; Pascal Ferraro; Daniel Gautheret; Claire Herrbach; Fabrice Leclerc; Antoine de Monte; Aïda Ouangraoua; Marie-France Sagot; Cédric Saule; Michel Termier; Claude Thermes; Hélène Touzet