DanMAC5: a browser of aggregated sequence variants from 8,671 whole genome sequenced Danish individuals
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 ...
Source: BMC Genetics - Category: Genetics & Stem Cells Authors: Karina Banasik, Peter L. M øller, Tanya R. Techlo, Peter C. Holm, G. Bragi Walters, Andrés Ingason, Anders Rosengren, Palle D. Rohde, Lisette J. A. Kogelman, David Westergaard, Troels Siggaard, Piotr J. Chmura, Mona A. Chalmer, Ólafur Þ. Magnússon, G Tags: Data note Source Type: research
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