# Impact of control selection strategies on GWAS results: a study of prostate cancer in the UK Biobank

**Authors:** Jingzhan Lu, Johan H Thygesen, Robin N Beaumont, Michael N Weedon, Harry D Green

PMC · DOI: 10.1093/bib/bbag102 · Briefings in Bioinformatics · 2026-03-09

## TL;DR

This study compares different control selection methods in prostate cancer GWAS to balance cost and effectiveness.

## Contribution

The novel contribution is evaluating matched vs random control selection in GWAS to optimize cost and statistical power.

## Key findings

- Matched controls showed greater consistency in identifying leading SNPs compared to random selection.
- Using matched controls reduced discovery power by ~30% compared to using all controls.
- Matched controls at a 1:4 ratio offer a cost-effective approach for targeted SNP analysis.

## Abstract

As genome-wide association studies (GWAS) studies move from array-based genotyping to whole exome and genome sequencing, there is a significant increase in cost. Applying an appropriate technique for the selection of which controls to include, in large studies where more potential controls are available than needed for the study, may be a useful technique for minimizing resource intensity whilst maintaining statistical power. We evaluated three control selection strategies in prostate cancer GWAS using 15 250 UK Biobank cases: (a) all controls, (b) matched controls, and (c) random selection. Both (b) and (c) achieved comparable power in detecting significant loci relative to (a), but matched controls (b) showed greater consistency in identifying leading single nucleotide polymorphisms (SNPs). However, using (b) matched controls reduced discovery power by ~30% compared with (a) all controls, highlighting a trade-off. Matching controls (1:4 ratio) offers a cost-effective approach for targeted SNP analysis across phenotypes but may miss novel associations.

## Linked entities

- **Diseases:** prostate cancer (MONDO:0005159)

## Full-text entities

- **Diseases:** Prostate Cancer (MESH:D011471), cancer (MESH:D009369), chromosome aneuploidy (MESH:D000782)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** 71120794G/A

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12971001/full.md

## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12971001/full.md

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Source: https://tomesphere.com/paper/PMC12971001