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Updated: Jul 28, 2025

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DanMAC5: a browser of aggregated sequence variants from 8,671 whole genome sequenced Danish individuals

Karina Banasik1, Peter L Møller2, Tanya R Techlo3

  • 1Translational Disease Systems Biology, Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B, DK-2200, Copenhagen N, Denmark. karina.banasik@cpr.ku.dk.

BMC Genomic Data
|May 27, 2023
PubMed
Abstract

Keywords:
BrowserMinor allele countsSequence variantsVariant interpretationWhole genome sequencing

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