Back

Deriving LD-adjusted GWAS summary statistics through linkage disequilibrium deconvolution

Nouira, A.; Favre Moiron, M.; Tournaire, M.; Verbanck, M.

2026-04-11 genetic and genomic medicine
10.64898/2026.04.10.26350574 medRxiv
Show abstract

Genome-wide association studies (GWAS) have identified numerous genetic variants associated with complex traits. However, linkage disequilibrium (LD) confounds these associations, leading to false positives where non-causal variants appear associated because they are correlated with nearby causal variants. This is particularly the case in highly polygenic traits where the genome can be saturated in causal variants. To address this issue, we propose LDeconv a method based on truncated singular value decomposition (SVD) that adjust GWAS summary statistics without requiring individual-level genotype data. This approach accounts for LD structure, isolates causal variants in high-LD regions, and improve the reliability of effect size estimates. We assess its performance through simulations across various LD scenarios, conduct extensive sensitivity analyses, and apply them to real GWAS data from the UK Biobank. Our results demonstrate that LDeconv effectively reduces false discoveries while preserving true associations, offering a robust framework for post-GWAS analysis.

Matching journals

The top 5 journals account for 50% of the predicted probability mass.

1
The American Journal of Human Genetics
206 papers in training set
Top 0.2%
18.5%
2
Bioinformatics
1061 papers in training set
Top 3%
10.1%
3
Nature Communications
4913 papers in training set
Top 22%
8.4%
4
PLOS Genetics
756 papers in training set
Top 2%
6.8%
5
Genetic Epidemiology
46 papers in training set
Top 0.1%
6.3%
50% of probability mass above
6
Nature Genetics
240 papers in training set
Top 1%
6.3%
7
Proceedings of the National Academy of Sciences
2130 papers in training set
Top 18%
3.9%
8
Scientific Reports
3102 papers in training set
Top 35%
3.7%
9
Genome Research
409 papers in training set
Top 1.0%
3.6%
10
Human Genetics and Genomics Advances
70 papers in training set
Top 0.1%
3.6%
11
PLOS Computational Biology
1633 papers in training set
Top 11%
3.1%
12
PLOS ONE
4510 papers in training set
Top 48%
2.1%
13
Cell Systems
167 papers in training set
Top 6%
1.9%
14
Frontiers in Genetics
197 papers in training set
Top 5%
1.7%
15
GENETICS
189 papers in training set
Top 0.6%
1.7%
16
Genome Biology
555 papers in training set
Top 5%
1.5%
17
Communications Biology
886 papers in training set
Top 13%
1.3%
18
Nucleic Acids Research
1128 papers in training set
Top 13%
1.3%
19
European Journal of Human Genetics
49 papers in training set
Top 1%
0.9%
20
NeuroImage
813 papers in training set
Top 6%
0.8%
21
Nature Human Behaviour
85 papers in training set
Top 4%
0.7%
22
Cell Genomics
162 papers in training set
Top 7%
0.7%
23
Bioinformatics Advances
184 papers in training set
Top 5%
0.6%