A protocol for applying low-coverage whole-genome sequencing data in structural variation studies

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Long-read Structural Variant Calling - Bioinformatics Documentation

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A multi-platform reference for somatic structural variation

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Genotyping by low-coverage whole-genome sequencing in intercross pedigrees from outbred founders: a cost-efficient approach, Genetics Selection Evolution

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Extremely low-coverage sequencing and imputation increases power for genome-wide association studies