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Frédéric Hospital

dblp:56/2193 · DBLP profile ↗
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3ranked-venue papers
1as first author
0since 2021 · last 2008
0000-0003-0825-4470ORCID · reported

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

Applied, interdisciplinary, general and emerging computing · 3 · 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
3 papers
Bioinformatics and computational biology · 100%

Topics — the 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › population genetics
population genetics simulation
0.112008
quantiNemo: an individual-based program to simulate quantitative traits with explicit genetic architecture in a dynamic metapopulation · Bioinform. 2008
Bioinformatics and computational biology › statistical genetics › genetic data simulation
quantitative trait simulation
0.112008
quantiNemo: an individual-based program to simulate quantitative traits with explicit genetic architecture in a dynamic metapopulation · Bioinform. 2008
Bioinformatics and computational biology
population genetics
0.021996
A general algorithm to compute multilocus genotype frequencies under various mating systems · Comput. Appl. Biosci. 1996
A FORTRAN program to simulate the evolution of genetic variability in a small population · Comput. Appl. Biosci. 1995
Bioinformatics and computational biology › statistical genetics
genetic linkage analysis
0.011996
A general algorithm to compute multilocus genotype frequencies under various mating systems · Comput. Appl. Biosci. 1996

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

stochastic simulation · 0.1individual-based simulation · 0.1recurrence equations · 0.0monte carlo simulation · 0.0meiosis simulation · 0.0
YearPublicationVenuePosition
2008 quantiNemo: an individual-based program to simulate quantitative traits with explicit genetic architecture in a dynamic metapopulation
abstract
UNLABELLED: quantiNemo is an individual-based, genetically explicit stochastic simulation program. It was developed to investigate the effects of selection, mutation, recombination and drift on quantitative traits with varying architectures in structured populations connected by migration and located in a heterogeneous habitat. quantiNemo is highly flexible at various levels: population, selection, trait(s) architecture, genetic map for QTL and/or markers, environment, demography, mating system, etc. quantiNemo is coded in C++ using an object-oriented approach and runs on any computer platform. AVAILABILITY: Executables for several platforms, user's manual, and source code are freely available under the GNU General Public License at http://www2.unil.ch/popgen/softwares/quantinemo.
Samuel Neuenschwander, Frédéric Hospital, Frédéric Guillaume, Jérôme Goudet
Bioinform.2
1996 A general algorithm to compute multilocus genotype frequencies under various mating systems
abstract
This paper provides a general method to derive algebraic expressions of genotype frequencies for multiple loci under various mating systems, including random mating, back-crossing, selfing, and full-sib mating. For each mating system, general equations are presented. In the case of three loci, comprehensive tables provide recurrence equations for genotype frequencies under random or self mating, and expected genotype frequencies after two generations of full-sib mating. Our results should prove useful in genetic linkage analysis.
Frédéric Hospital, Christine Dillmann, A. E. Melchinger
Comput. Appl. Biosci.1
1995 A FORTRAN program to simulate the evolution of genetic variability in a small population
abstract
This paper presents a FORTRAN-77 program that performs Monte Carlo simulation of the evolution of genetic structure in a small population under selection. The aim is to study the possibility of foreseeing a response plateau in a theoretical population, depending on population size and management, and to apply this to small populations actually selected, to predict a possible exhaustion of genetic variability. A set of subroutines describing the different steps in a selection cycle (birth, expression of phenotypic value, genetic evaluation, selection, reproduction, death) is available and the user can choose the sequence of subroutines, the characteristics of individuals submitted to each step, and also build more personal subroutines if necessary. The program is based on the generation of exact genotypes and their transmission from parents to offspring, through simulation of meiosis and pairing of gametes. Parameters concerning the genome, the initial structure of the population and its management are required. The genetic mean and variance of the population for each new cycle of selection are given as outputs. Examples of applications are given and discussed.
F. Fournet, Frédéric Hospital, J. M. Elsen
Comput. Appl. Biosci.2