DEV - Switch reference genome to hg38 for raredisease#4871
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DEV - Switch reference genome to hg38 for raredisease#4871
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dnil
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Feb 4, 2026
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| Old codes find the light, Newer maps trace hidden flaws, Healing starts with data. No newline at end of file |
dnil
reviewed
Feb 4, 2026
Co-authored-by: Daniel Nilsson <daniel.k.nilsson@gmail.com>
change raredisease genome version for bed version fetch to hg38 --------- Co-authored-by: kedhammar <alfred.kedhammar@scilifelab.se>
Use Scout38 in the ConfiguratorFactory for the creation of managed_variants and gene_panel files for raredisease --------- Co-authored-by: Rasmus Burge <80392398+RasmusBurge-CG@users.noreply.github.com> Co-authored-by: Sebastian Diaz <juan.sebastian.diaz.boada@scilifelab.se> Co-authored-by: kedhammar <alfred.kedhammar@scilifelab.se>
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