SAIGE software on GitHub in support of 'Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction'

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SAIGE software on GitHub

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17 Research products, page 1 of 2

Whole exome sequencing identified six novel genes for depressive symptoms
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X‐chromosome-wide association study for Alzheimer’s disease
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Large-scale whole-exome sequencing analyses identified protein-coding variants associated with immune-mediated diseases in 350,770 adults
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Scalable mixed model methods for set-based association studies on large-scale categorical data analysis and its application to exome-sequencing data in UK Biobank
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Exome sequencing identifies novel genetic variants associated with varicose veins
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Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction
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Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum
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Exome sequencing identifies genes associated with sleep-related traits
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Large-scale whole-exome sequencing of neuropsychiatric diseases and traits in 350,770 adults
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Genetic associations of protein-coding variants in venous thromboembolism
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