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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https://scilifelab.figshare.com/articles/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/12058275
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资源简介：
De novo assembly of two individuals from the SweGen dataset
提供机构：
Uppsala University
创建时间：
2018-09-21
