Demo Data from VLDB 2026 / reviewers in the wild / expert
Benjamin Horstman
dblp:95/9778
· DBLP profile ↗
1ranked-venue papers
0as first author
0since 2021 · last 2011
—ORCID · none
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 1
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 3 heaviest of 3, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › genomics › genome-wide association study
epistasis detection |
0.1 | 1 | 2011 | Detecting epistatic effects in association studies at a genomic level based on an ensemble approach · Bioinform. 2011 |
Bioinformatics and computational biology › statistical genetics
gene-gene interaction |
0.1 | 1 | 2011 | Detecting epistatic effects in association studies at a genomic level based on an ensemble approach · Bioinform. 2011 |
Bioinformatics and computational biology › genomics
genome-wide association study |
0.1 | 1 | 2011 | Detecting epistatic effects in association studies at a genomic level based on an ensemble approach · Bioinform. 2011 |
Methods — techniques the papers use, named apart from their topics
permutation testing · 0.1gini impurity · 0.1ensemble learning · 0.1adaboost · 0.1
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2011 | Detecting epistatic effects in association studies at a genomic level based on an ensemble approachabstractMOTIVATION: Most complex diseases involve multiple genes and their interactions. Although genome-wide association studies (GWAS) have shown some success for identifying genetic variants underlying complex diseases, most existing studies are based on limited single-locus approaches, which detect single nucleotide polymorphisms (SNPs) essentially based on their marginal associations with phenotypes. RESULTS: In this article, we propose an ensemble approach based on boosting to study gene-gene interactions. We extend the basic AdaBoost algorithm by incorporating an intuitive importance score based on Gini impurity to select candidate SNPs. Permutation tests are used to control the statistical significance. We have performed extensive simulation studies using three interaction models to evaluate the efficacy of our approach at realistic GWAS sizes, and have compared it with existing epistatic detection algorithms. Our results indicate that our approach is valid, efficient for GWAS and on disease models with epistasis has more power than existing programs. CONTACT: [email protected]. Jing Li 0002, Benjamin Horstman, Yixuan Chen 0001 |
Bioinform. | 2 |