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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
UnknownRare variant contribution to the heritability of coronary artery disease.
Not available
S-EPMC11464707 | biostudies-literature
UnknownInsights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.
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S-EPMC9593435 | 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
UnknownA framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies.
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S-EPMC10008172 | biostudies-literature
UnknownImputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33.
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S-EPMC4240198 | biostudies-literature
UnknownGlobal burden of 292 causes of death in 204 countries and territories and 660 subnational locations, 1990-2023: a systematic analysis for the Global Burden of Disease Study 2023.
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S-EPMC12535838 | biostudies-literature
UnknownBurden of 375 diseases and injuries, risk-attributable burden of 88 risk factors, and healthy life expectancy in 204 countries and territories, including 660 subnational locations, 1990-2023: a systematic analysis for the Global Burden of Disease Study 2023.
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S-EPMC12535840 | biostudies-literature
UnknownImplicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis.
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S-EPMC9793579 | biostudies-literature
UnknownGuidelines for the use and interpretation of assays for monitoring autophagy (3rd edition).
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S-EPMC4835977 | biostudies-literature
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