Demo Data from EDBT 2026 / reviewers in the wild / expert
Franz Rüschendorf
dblp:75/5693
· DBLP profile ↗
2ranked-venue papers
1as first author
0since 2021 · last 2007
0000-0001-5640-810XORCID · corroborated
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
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › statistical genetics
genetic linkage analysis |
0.1 | 2 | 2007 | Linkage analysis using sex-specific recombination fractions with GENEHUNTER-MODSCORE · Bioinform. 2007 ALOHOMORA: a tool for linkage analysis using 10K SNP array data · Bioinform. 2005 |
Bioinformatics and computational biology › population genetics
genetics |
0.1 | 1 | 2007 | Linkage analysis using sex-specific recombination fractions with GENEHUNTER-MODSCORE · Bioinform. 2007 |
Bioinformatics and computational biology › statistical genetics › genotype data analysis
genotype quality control |
0.0 | 1 | 2005 | ALOHOMORA: a tool for linkage analysis using 10K SNP array data · Bioinform. 2005 |
Methods — techniques the papers use, named apart from their topics
simulation · 0.1linkage analysis · 0.1
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2007 | Linkage analysis using sex-specific recombination fractions with GENEHUNTER-MODSCOREabstractMOTIVATION: Sex-specific marker maps have become increasingly available. We have implemented the usage of sex-specific recombination frequencies in the GENEHUNTER-MODSCORE program that performs multipoint linkage analysis. Furthermore, we have devised a consistent method to choose the combinations of male and female genetic positions at which linkage scores should be calculated. Marker coordinates can be read automatically from publicly available genetic maps. RESULTS: In a MOD-score analysis of the COGA dataset provided for Genetic Analysis Workshop 14, the highest linkage peak on chromosome 1 further increases when using sex-specific maps, while some smaller peaks are decreased. Simulations confirm that the MOD score can be biased when a sex-averaged instead of the correct sex-specific map is employed. This shows that an adequate modeling of the female:male ratio of genetic distances is important, especially for complex traits. AVAILABILITY: The new version of GENEHUNTER-MODSCORE can be downloaded from the following website: http://www.staff.uni-marburg.de/~strauchk/software.html Johannes Dietter, Manuel Mattheisen, Robert Fürst, Franz Rüschendorf, Thomas F. Wienker, Konstantin Strauch |
Bioinform. | 4 |
| 2005 | ALOHOMORA: a tool for linkage analysis using 10K SNP array dataabstractSUMMARY: ALOHOMORA is a software tool designed to facilitate genome-wide linkage studies performed with high-density single nucleotide polymorphism (SNP) marker panels such as the Affymetrix GeneChip(R) Human Mapping 10K Array. Genotype data are converted into appropriate formats for a number of common linkage programs and subjected to standard quality control routines before linkage runs are started. ALOHOMORA is written in Perl and may be used to perform state-of-the-art linkage scans in small and large families with any genetic model. Options for using different genetic maps or ethnicity-specific allele frequencies are implemented. Graphic outputs of whole-genome multipoint LOD score values are provided for the entire dataset as well as for individual families. AVAILABILITY: ALOHOMORA is available free of charge for non-commercial research institutions. For more details, see http://gmc.mdc-berlin.de/alohomora/ Franz Rüschendorf, Peter J. Nürnberg |
Bioinform. | 1 |