Demonstration venue · read-only. Every page can be browsed; the buttons that would change it are switched off. Create an account to run TaxoReview on your own data. A simulation from public publication records: the people listed were not invited and did not agree to review.
? Tutorial for this page

Alain Hénaut

dblp:06/1038 · DBLP profile ↗
← Back
7ranked-venue papers
1as first author
0since 2021 · last 2002
—ORCID · none

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 6Artificial intelligence and machine learning · 1 · 1 first-author

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
5 papers
Bioinformatics and computational biology · 100%

Topics — the 12 heaviest of 12, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › gene expression analysis
differential expression analysis
0.012002
GeneANOVA-gene expression analysis of variance · Bioinform. 2002
Bioinformatics and computational biology
gene expression analysis
0.012002
GeneANOVA-gene expression analysis of variance · Bioinform. 2002
Bioinformatics and computational biology › genomics
genome analysis
0.011997
Detection of significant patterns by compression algorithms: the case of approximate tandem repeats in DNA sequences · Comput. Appl. Biosci. 1997
Bioinformatics and computational biology › sequence analysis › repeat detection
tandem repeat detection
0.011997
Detection of significant patterns by compression algorithms: the case of approximate tandem repeats in DNA sequences · Comput. Appl. Biosci. 1997
Bioinformatics and computational biology › sequence analysis › sequence assembly
contig assembly
0.011994
A global approach for contig construction · Comput. Appl. Biosci. 1994
Bioinformatics and computational biology › sequence analysis
sequence assembly
0.011994
A global approach for contig construction · Comput. Appl. Biosci. 1994
Bioinformatics and computational biology › sequence analysis › sequence comparison
alignment-free sequence comparison
0.011993
Dot-plot comparisons by multivariate analysis (DOCMA): a tool for classifying protein sequences · Comput. Appl. Biosci. 1993
Bioinformatics and computational biology › biological database
metabolic pathway database
0.011993
METALGEN.DB: metabolism linked to the genome of Escherichia coli, a graphics-oriented database · Comput. Appl. Biosci. 1993
Bioinformatics and computational biology
protein sequence analysis
0.011993
Dot-plot comparisons by multivariate analysis (DOCMA): a tool for classifying protein sequences · Comput. Appl. Biosci. 1993
Bioinformatics and computational biology › protein function prediction › protein classification
protein sequence classification
0.011993
Dot-plot comparisons by multivariate analysis (DOCMA): a tool for classifying protein sequences · Comput. Appl. Biosci. 1993
Bioinformatics and computational biology › sequence analysis › sequence comparison
dot plot sequence comparison
0.011993
Dot-plot comparisons by multivariate analysis (DOCMA): a tool for classifying protein sequences · Comput. Appl. Biosci. 1993
Bioinformatics and computational biology › systems biology
metabolic network modeling
0.011993
METALGEN.DB: metabolism linked to the genome of Escherichia coli, a graphics-oriented database · Comput. Appl. Biosci. 1993

Methods — techniques the papers use, named apart from their topics

ANOVA · 0.0compression algorithms · 0.0dynamic programming · 0.0relational database · 0.0multivariate analysis · 0.0graphical interface · 0.0dynamic clustering · 0.0chi-squared analysis · 0.0
YearPublicationVenuePosition
2002 GeneANOVA-gene expression analysis of variance
abstract
Abstract Summary: GeneANOVA is an ANOVA-based software devoted to the analysis of gene expression data. Availability: GeneANOVA is freely available on request for non-commercial use. Contact: [email protected]
Gilles Didier, Pierre Brézellec, Elisabeth Remy, Alain Hénaut
Bioinform.4
1997 Detection of significant patterns by compression algorithms: the case of approximate tandem repeats in DNA sequences
abstract
MOTIVATION: Compression algorithms can be used to analyse genetic sequences. A compression algorithm tests a given property on the sequence and uses it to encode the sequence: if the property is true, it reveals some structure of the sequence which can be described briefly, this yields a description of the sequence which is shorter than the sequence of nucleotides given in extenso. The more a sequence is compressed by the algorithm, the more significant is the property for that sequence. RESULTS: We present a compression algorithm that tests the presence of a particular type of dosDNA (defined ordered sequence-DNA): approximate tandem repeats of small motifs (i.e. of lengths < 4). This algorithm has been experimented with on four yeast chromosomes. The presence of approximate tandem repeats seems to be a uniform structural property of yeast chromosomes.
Eric Rivals, Olivier Delgrange, Jean-Paul Delahaye, Max Dauchet, Marie-Odile Delorme, Alain Hénaut, Emmanuelle Ollivier
Comput. Appl. Biosci.6
1994 A global approach for contig construction
abstract
A program for assembling sequences by using a global approach has been developed. By successive steps, a more and more precise classification of DNA fragments permits the positioning of the sequences on the contig; after having detected the pairs of overlapping sequences, groups are formed such that all sequences in a group overlap. Sequences common to several groups enable the groups to be ordered in a series. Ambiguities in the order of groups can arise at this stage, due to the presence of repeated fragments; different solutions are then proposed. Putting the groups into order leads to a preclassification of sequences. The fragments are then aligned by group, by searching for words common to all sequences in the group, and using an algorithm of dynamic programming. A detailed example on a set of nine sequences accompanies the description of the method.
A. Gleizes, Alain Hénaut
Comput. Appl. Biosci.2
1993 Dot-plot comparisons by multivariate analysis (DOCMA): a tool for classifying protein sequences
abstract
A method aimed at classifying protein sequences without resorting to pairwise alignment is presented. Called DOCMA (DOt-plot Comparisons by Multivariate Analysis), it is based on a multivariate analysis of the pairwise dot-plots between all the sequences in the set. The dot-plots are first simplified by considering only the projections of the 'diagonal' segments of similarity onto the axes. From these projections a data matrix is built, in which each column is representative of the comparisons of one given sequence with all the other ones. This data matrix is then transformed into a distance matrix by a chi-squared analysis, from which the coordinates of the sequences in an orthonormal Euclidean space are obtained. The sequences are finally classified by a dynamic clustering procedure followed by a search for strong clusters. Application of this method to protein families such as the globins, the cytochromes c and the aminoacyl-tRNA synthetases shows that it is quite effective in delineating subgroups that contain even distantly related sequences.
Claudine Devauchelle, Alain Hénaut, Jean-Loup Risler
Comput. Appl. Biosci.2
1993 METALGEN.DB: metabolism linked to the genome of Escherichia coli, a graphics-oriented database
abstract
The table of 'biochemical pathways' published by Boehringer is considered as the most exhaustive document dealing with intermediary metabolism. The present work consisted of constructing a database in which is collected everything known to date about intermediary metabolism: metabolic pathways, bioreactions, metabolites, enzymatic activities, genes and regulation. Data on genes make it possible to establish a link with existing computer structures specialized for genomic sequences. The present structure of the database presented here consists of three environments. The first environment is graphic; it is modeled upon the Boehringer table, but is more convenient to use. The second environment provides the user with all kinds of manipulations of data (entries, corrections, deletions, consistency, limiting redundancy, etc.). These operations either are automatic or depend on a user-friendly interface (menus selected with the mouse) and so allow biologists at all levels to use the database and to develop it for their own particular needs. Finally, the third environment offers various procedures that make it possible to carry out multicriteria research on all the data in the database at once. This database can thus be substituted for the Boehringer table as a standard reference. It is also a tool that can be used to develop information systems not only in the domain of metabolism but also in the study of genomes (modeling, analysis of data, predictions, etc.).
T. Rouxel, Antoine Danchin, Alain Hénaut
Comput. Appl. Biosci.3
1988 Merging of distance matrices and classification by dynamic clustering
abstract
The graphical representation of distance matrices in a Euclidean space allows the merging of two distance matrices since the two matrices have shared elements. The graphical representation of the merging of the two distance matrices is associated with a robust method of classification that allows one to distinguish species for which membership to a cluster cannot be established with certainty. These possibilities are exploited to test the consistency of phylogenetic trees, and to establish exact relations between species for which one possesses different independent distance measurements (distance matrices established from several types of sequences for instance). The whole set of programs is written in BASIC and runs on microcomputers.
Marie-Odile Delorme, Alain Hénaut
Comput. Appl. Biosci.2
1988 Distance matrix comparison and tree construction
Alain Hénaut, Marie-Odile Delorme
Pattern Recognit. Lett.1