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UnknownLD Score regression distinguishes confounding from polygenicity in genome-wide association studies.
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S-EPMC4495769 | biostudies-literature
UnknownModeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores.
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S-EPMC4596916 | biostudies-literature
UnknownPowerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies.
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S-EPMC10084891 | biostudies-literature
UnknownContrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis.
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S-EPMC4666835 | biostudies-literature
UnknownA framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies.
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S-EPMC10008172 | biostudies-literature
UnknownDynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale.
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S-EPMC7483769 | biostudies-literature
UnknownAnalysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for Thirteen Cancer Types.
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S-EPMC4806328 | biostudies-literature
UnknownThe seventh blind test of crystal structure prediction: structure ranking methods.
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S-EPMC11789160 | biostudies-literature
UnknownWhole genome sequence analysis of blood lipid levels in >66,000 individuals.
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S-EPMC9553944 | biostudies-literature
UnknownCharacteristics and Outcomes of Individuals With Pre-existing Kidney Disease and COVID-19 Admitted to Intensive Care Units in the United States.
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S-EPMC7501875 | biostudies-literature
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