Demo Data from VLDB 2026 / reviewers in the wild / expert
Carolin Artmann
dblp:394/1838
· DBLP profile ↗
1ranked-venue papers
0as first author
1since 2021 · last 2022
—ORCID · none
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 1 · 1 since 2021
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 2 heaviest of 2, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › genomics
genome-wide association study |
0.6 | 1 | 2022 | Efficient permutation-based genome-wide association studies for normal and skewed phenotypic distributions · Bioinform. 2022 |
Bioinformatics and computational biology › statistical genetics
linear mixed model |
0.6 | 1 | 2022 | Efficient permutation-based genome-wide association studies for normal and skewed phenotypic distributions · Bioinform. 2022 |
Methods — techniques the papers use, named apart from their topics
tensor computation · 0.6permutation testing · 0.6linear mixed model · 0.6
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2022 | Efficient permutation-based genome-wide association studies for normal and skewed phenotypic distributionsabstractMOTIVATION: Genome-wide association studies (GWAS) are an integral tool for studying the architecture of complex genotype and phenotype relationships. Linear mixed models (LMMs) are commonly used to detect associations between genetic markers and a trait of interest, while at the same time allowing to account for population structure and cryptic relatedness. Assumptions of LMMs include a normal distribution of the residuals and that the genetic markers are independent and identically distributed-both assumptions are often violated in real data. Permutation-based methods can help to overcome some of these limitations and provide more realistic thresholds for the discovery of true associations. Still, in practice, they are rarely implemented due to the high computational complexity. RESULTS: We propose permGWAS, an efficient LMM reformulation based on 4D tensors that can provide permutation-based significance thresholds. We show that our method outperforms current state-of-the-art LMMs with respect to runtime and that permutation-based thresholds have lower false discovery rates for skewed phenotypes compared to the commonly used Bonferroni threshold. Furthermore, using permGWAS we re-analyzed more than 500 Arabidopsis thaliana phenotypes with 100 permutations each in less than 8 days on a single GPU. Our re-analyses suggest that applying a permutation-based threshold can improve and refine the interpretation of GWAS results. AVAILABILITY AND IMPLEMENTATION: permGWAS is open-source and publicly available on GitHub for download: https://github.com/grimmlab/permGWAS. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Maura John, Markus J. Ankenbrand, Carolin Artmann, Jan A. Freudenthal, Arthur Korte, Dominik G. Grimm |
Bioinform. | 3 |