Article
DanMAC5: a browser of aggregated sequence variants from 8,671 whole genome sequenced Danish individuals.
BMC genomic data - 27 May 2023
Banasik Karina, Møller Peter L, Techlo Tanya R, Holm Peter C, Walters G Bragi, Ingason Andrés, Rosengren Anders, Rohde Palle D, Kogelman Lisette J A, Westergaard David, Siggaard Troels, Chmura Piotr J, Chalmer Mona A, Magnússon Ólafur Þ, Þórisson Guðmundur Á, Stefánsson Hreinn, Guðbjartsson Daníel F, Stefánsson Kári, Olesen Jes, Winther Simon, Bøttcher Morten, Brunak Søren, Werge Thomas, Nyegaard Mette, Hansen Thomas F
Abstract excerpt
OBJECTIVES: Allele counts of sequence variants obtained by whole genome sequencing (WGS) often play a central role in interpreting the results of genetic and genomic research. However, such variant counts are not readily available for individuals in the Danish population. Here, we present a dataset with allele counts for sequence variants (single nucleotide variants (SNVs) and indels) identified from WGS of 8,671...
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