Wei-Yang Bai

A proteome atlas of structural variation and VNTR effects on complex traits and diseases

The paper imputes structural variants and VNTRs in UK Biobank participants to identify their effects on plasma protein abundances and complex traits, finding significant associations and regulatory impacts.

SEAD: an augmented reference panel with 22,134 haplotypes boosts the rare variants imputation and GWAS analysis in Asian population

The paper introduces SEAD, an Asian reference panel that improves rare variant imputation and GWAS analysis, identifying a novel association between SNTG1 and hip BMD.

Genomic analyses of 10,376 individuals provides comprehensive map of genetic variations, structure and reference haplotypes for Chinese population

The paper presents genomic analyses of 10,376 Chinese individuals, identifying novel genetic variations and providing a reference haplotype map, along with an imputation server for improved accuracy.

Genotype Imputation and Reference Panel: A Systematic Evaluation

The paper evaluates genotype imputation accuracy across Han Chinese and European populations using 394 reference panels, finding optimal diversity levels and highlighting the need for better Chinese reference panels.