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

E. Ollivier

dblp:53/5291 · DBLP profile ↗
← Back
2ranked-venue papers
1as first author
0since 2021 · last 1991
—ORCID · none

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

Applied, interdisciplinary, general and emerging computing · 2 · 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
2 papers
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
protein sequence analysis
0.021991
'Multifrequency' location and clustering of sequence patterns from proteins · Comput. Appl. Biosci. 1991
A scale-independent signal processing method for sequence analysis · Comput. Appl. Biosci. 1990
Bioinformatics and computational biology › protein analysis › protein bioinformatics
protein family
0.011991
'Multifrequency' location and clustering of sequence patterns from proteins · Comput. Appl. Biosci. 1991
Bioinformatics and computational biology › protein function prediction › protein classification
protein family classification
0.011990
A scale-independent signal processing method for sequence analysis · Comput. Appl. Biosci. 1990

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

signal processing · 0.0clustering · 0.0fourier analysis · 0.0
YearPublicationVenuePosition
1991 'Multifrequency' location and clustering of sequence patterns from proteins
abstract
In previous work, we have shown that a set of characteristics, defined as (code frequency) pairs, can be derived from a protein family by the use of a signal-processing method. This method enables the location and extraction of sequence patterns by taking into account each (code frequency) pair individually. In the present paper, we propose to extend this method in order to detect and visualize patterns by taking into account several pairs simultaneously. Two 'multifrequency' methods are described. The first one is based on a rewriting of the sequences with new symbols which summarize the frequency information. The second method is based on a clustering of the patterns associated with each pair. Both methods lead to the definition of significant consensus sequences. Some results obtained with calcium-binding proteins and serine proteases are also discussed.
E. Ollivier, Henry Soldano, Alain Viari
Comput. Appl. Biosci.1
1990 A scale-independent signal processing method for sequence analysis
abstract
In this paper, we present methods to detect and localize patterns in biologically related protein sequences (family). The patterns common to the sequences of the family are detected by using Fourier analysis. No previous scales (codes) are needed, they are actually produced as a result of the analysis procedure, together with the frequencies of the Fourier decompositions. Characteristic features of the family are thus expressed as (code-frequency) pairs. Various tools are proposed in order to localize the patterns, to compare the codes, and to evaluate the proximity of an arbitrary sequence to the investigated family. The general strategy is illustrated on a family composed of calcium-binding proteins.
Alain Viari, Henry Soldano, E. Ollivier
Comput. Appl. Biosci.3