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Timothy A. Myers

dblp:294/5055 · DBLP profile ↗
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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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › genomics
genome-wide association study
0.512021
PCAmatchR: a flexible R package for optimal case-control matching using weighted principal components · Bioinform. 2021
Bioinformatics and computational biology
genomics
0.512021
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
0.512021
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
YearPublicationVenuePosition
2021 PCAmatchR: a flexible R package for optimal case-control matching using weighted principal components
abstract
SUMMARY: 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