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

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Data Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10225079/
https://www.ncbi.nlm.nih.gov/pubmed/37244984
http://dx.doi.org/10.1186/s12863-023-01132-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10225079/
https://www.ncbi.nlm.nih.gov/pubmed/37244984
http://dx.doi.org/10.1186/s12863-023-01132-7

Ejemplares similares