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Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits

BioinformaticsStructural VariantsLong-read SequencingAllelic VariantHuman DiseasesNext-generation SequencingGeneticsMolecular GeneticsDisease Gene IdentificationGenomicsSystems BiologyMedicineSequencingVariant Interpretation