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Data from: De novo assembly of two Swedish genomes reveals missing segments from the human GRCh38 reference and improves variant calling of population-scale sequencing data

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posted on 21.09.2018, 00:00 by Adam Ameur, Ulf Gyllensten
De novo assembly of two individuals from the SweGen dataset

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Uppsala University

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adam.ameur@igp.uu.se

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