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Ameur A, Che H, Martin M, Bunikis I, Dahlberg J, Höijer I, Häggqvist S, Vezzi F, Nordlund J, Olason P, et al. De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data. Genes. 2018; 9(10):486. https://doi.org/10.3390/genes9100486

Ameur, Adam, Huiwen Che, Marcel Martin, Ignas Bunikis, Johan Dahlberg, Ida Höijer, Susana Häggqvist, Francesco Vezzi, Jessica Nordlund, Pall Olason, and et al. 2018. "De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data" Genes 9, no. 10: 486. https://doi.org/10.3390/genes9100486

Ameur, A., Che, H., Martin, M., Bunikis, I., Dahlberg, J., Höijer, I., Häggqvist, S., Vezzi, F., Nordlund, J., Olason, P., Feuk, L., & Gyllensten, U. (2018). De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data. Genes, 9(10), 486. https://doi.org/10.3390/genes9100486