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Data · dataset · 2018

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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De novo assembly of two individuals from the SweGen dataset

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Catalogue records · 1

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Inferred from text
Sequencing 75%
Provenance · 1 source records, 8 field assertions
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Researchdata.seoai:researchdata.se:doi-10-17044-nbis-g000006/010 d agoJSON v1
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concepts[modality].local:modality:sequencingenrichment · researchdata sekeyword-concept-rules@1.0.0title+description (75%)
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