Demo Data from VLDB 2026 / reviewers in the wild / expert
Timothy A. Myers
dblp:294/5055
· DBLP profile ↗
1ranked-venue papers
0as first author
1since 2021 · last 2021
—ORCID · unresolved
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 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 |
0.5 | 1 | 2021 | PCAmatchR: a flexible R package for optimal case-control matching using weighted principal components · Bioinform. 2021 |
Bioinformatics and computational biology
genomics |
0.5 | 1 | 2021 | PCAmatchR: a flexible R package for optimal case-control matching using weighted principal components · Bioinform. 2021 |
Bioinformatics and computational biology › population genetics
population stratification correction |
0.5 | 1 | 2021 | PCAmatchR: a flexible R package for optimal case-control matching using weighted principal components · Bioinform. 2021 |
Methods — techniques the papers use, named apart from their topics
principal component analysis · 0.5mahalanobis distance · 0.5
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2021 | PCAmatchR: a flexible R package for optimal case-control matching using weighted principal componentsabstractSUMMARY: A concern when conducting genome-wide association studies (GWAS) is the potential for population stratification, i.e. ancestry-based genetic differences between cases and controls, that if not properly accounted for, could lead to biased association results. We developed PCAmatchR as an open source R package for performing optimal case-control matching using principal component analysis (PCA) to aid in selecting controls that are well matched by ancestry to cases. PCAmatchR takes user supplied PCA outputs and selects matching controls for cases by utilizing a weighted Mahalanobis distance metric which weights each principal component by the percentage of genetic variation explained. Results from the 1000 Genomes Project data demonstrate both the functionality and performance of PCAmatchR for selecting matching controls for case populations as well as reducing inflation of association test statistics. PCAmatchR improves genomic similarity between matched cases and controls, which minimizes the effects of population stratification in GWAS analyses. AVAILABILITY AND IMPLEMENTATION: PCAmatchR is freely available for download on GitHub (https://github.com/machiela-lab/PCAmatchR) or through CRAN (https://CRAN.R-project.org/package=PCAmatchR). SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Derek W. Brown, Timothy A. Myers, Mitchell J. Machiela |
Bioinform. | 2 |