Demo Data from EDBT 2026 / reviewers in the wild / expert
Leif Schauser
dblp:98/2785
· DBLP profile ↗
2ranked-venue papers
0as first author
0since 2021 · last 2006
0000-0003-0675-8077ORCID · corroborated
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 2
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
1 paper |
Bioinformatics and computational biology · 100% |
Topics — the 4 heaviest of 5, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › statistical genetics › genetic association study
association mapping |
0.1 | 1 | 2006 | GeneRecon - a coalescent based tool for fine-scale association mapping · Bioinform. 2006 |
Bioinformatics and computational biology › population genetics
genetics |
0.1 | 1 | 2006 | GeneRecon - a coalescent based tool for fine-scale association mapping · Bioinform. 2006 |
Bioinformatics and computational biology › population genetics › coalescent theory
coalescent model |
0.0 | 1 | 2006 | GeneRecon - a coalescent based tool for fine-scale association mapping · Bioinform. 2006 |
Bioinformatics and computational biology
population genetics |
0.0 | 1 | 2006 | GeneRecon - a coalescent based tool for fine-scale association mapping · Bioinform. 2006 |
Methods — techniques the papers use, named apart from their topics
metropolis-hastings sampling · 0.1coalescent model · 0.1
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2006 | GeneRecon - a coalescent based tool for fine-scale association mappingabstractUNLABELLED: GeneRecon is a tool for fine-scale association mapping using a coalescence model. GeneRecon takes as input case-control data from phased or unphased SNP and microsatellite genotypes. The posterior distribution of disease locus position is obtained by Metropolis-Hastings sampling in the state space of genealogies. Input format, search strategy and the sampled statistics can be configured through the Guile Scheme programming language embedded in GeneRecon, making GeneRecon highly configurable. AVAILABILITY: The source code for GeneRecon, written in C++ and Scheme, is available under the GNU General Public License (GPL) at http://www.birc.au.dk/~mailund/GeneRecon CONTACT: [email protected]. Thomas Mailund, Mikkel H. Schierup, Christian N. S. Pedersen, Jesper N. Madsen, Jotun Hein, Leif Schauser |
Bioinform. | 6 |
| 2005 | CoaSim: A flexible environment for simulating genetic data under coalescent modelsabstractBACKGROUND: Coalescent simulations are playing a large role in interpreting large scale intra-specific sequence or polymorphism surveys and for planning and evaluating association studies. Coalescent simulations of data sets under different models can be compared to the actual data to test the importance of different evolutionary factors and thus get insight into these. RESULTS: We have created the CoaSim application as a flexible environment for Monte Carlo simulation of various types of genetic data under equilibrium and non-equilibrium coalescent processes for a variety of applications. Interaction with the tool is through the Guile version of the Scheme scripting language. Scheme scripts for many standard and advanced applications are provided and these can easily be modified by the user for a much wider range of applications. A graphical user interface with less functionality and flexibility is also included. It is primarily intended as an exploratory and educational tool CONCLUSION: CoaSim is a powerful tool because of its flexibility and ease of use. This is illustrated through very varied uses of the application, e.g. evaluation of association mapping methods, parametric bootstrapping, and design and choice of markers for specific questions. Thomas Mailund, Mikkel H. Schierup, Christian N. S. Pedersen, Peter J. M. Mechlenborg, Jesper N. Madsen, Leif Schauser |
BMC Bioinform. | 6 |