Discovering non-additive heritability using additive GWAS summary statistics

被引:0
|
作者
Pattillo Smith, Samuel [1 ,2 ,3 ,4 ]
Darnell, Gregory [1 ,5 ]
Udwin, Dana [6 ]
Stamp, Julian [1 ]
Harpak, Arbel [3 ,4 ]
Ramachandran, Sohini [1 ,2 ,7 ]
Crawford, Lorin [1 ,6 ,8 ]
机构
[1] Brown Univ, Ctr Computat Mol Biol, Providence, RI 02912 USA
[2] Brown Univ, Dept Ecol & Evolutionary Biol, Providence, RI USA
[3] Univ Texas Austin, Dept Integrat Biol, Austin, TX USA
[4] Univ Texas Austin, Dept Populat Hlth, Austin, TX USA
[5] Brown Univ, Inst Computat & Expt Res Math, Providence, RI USA
[6] Brown Univ, Dept Biostat, Providence, RI 02912 USA
[7] Brown Univ, Data Sci Inst, Providence, RI USA
[8] Microsoft, Cambridge, MA 02142 USA
来源
ELIFE | 2024年 / 13卷
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
interactions; summary statistics; non-additive effects; heritability; BAYESIAN VARIABLE SELECTION; HUMAN COMPLEX TRAITS; MISSING HERITABILITY; SNP-HERITABILITY; REGRESSION; ASSOCIATION; DOMINANCE; EPISTASIS; ARCHITECTURE; VARIANTS;
D O I
10.7554/eLife.90459; 10.7554/eLife.90459.sa1; 10.7554/eLife.90459.sa2
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
LD score regression (LDSC) is a method to estimate narrow-sense heritability from genome-wide association study (GWAS) summary statistics alone, making it a fast and popular approach. In this work, we present interaction-LD score (i-LDSC) regression: an extension of the original LDSC framework that accounts for interactions between genetic variants. By studying a wide range of generative models in simulations, and by re-analyzing 25 well-studied quantitative phenotypes from 349,468 individuals in the UK Biobank and up to 159,095 individuals in BioBank Japan, we show that the inclusion of a cis-interaction score (i.e. interactions between a focal variant and proximal variants) recovers genetic variance that is not captured by LDSC. For each of the 25 traits analyzed in the UK Biobank and BioBank Japan, i-LDSC detects additional variation contributed by genetic interactions. The i-LDSC software and its application to these biobanks represent a step towards resolving further genetic contributions of sources of non-additive genetic effects to complex trait variation.
引用
收藏
页数:32
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