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UnknownThe genetic determinants of recurrent somatic mutations in 43,693 blood genomes.
Not available
S-EPMC10132750 | biostudies-literature
UnknownDynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale.
Not available
S-EPMC7483769 | biostudies-literature
UnknownPowerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies.
Not available
S-EPMC10084891 | biostudies-literature
UnknownWhole genome sequence analysis of blood lipid levels in >66,000 individuals.
Not available
S-EPMC9553944 | biostudies-literature
UnknownAberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.
Not available
S-EPMC10360040 | biostudies-literature
UnknownA framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies.
Not available
S-EPMC10008172 | biostudies-literature
UnknownChromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.
Not available
S-EPMC8042019 | biostudies-literature
UnknownSequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.
Not available
S-EPMC7875770 | biostudies-literature
UnknownGuidelines for the use and interpretation of assays for monitoring autophagy (3rd edition).
Not available
S-EPMC4835977 | biostudies-literature
UnknownDisease burden attributable to intimate partner violence against females and sexual violence against children in 204 countries and territories, 1990-2023: a systematic analysis for the Global Burden of Disease Study 2023.
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S-EPMC12775558 | biostudies-literature
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