WEGS: a cost-effective sequencing method for genetic studies combining high-depth whole exome and low-depth whole genome
Claude Bhérer, Robert J. M. Eveleigh, Katerina Trajanoska, Janick St-Cyr, Antoine Paccard, Praveen Nadukkalam Ravindran, Elizabeth A. Caron, Nimara Bader Asbah, Peyton McClelland, Clare Wei, Iris Baumgärtner, Marc Schindewolf, Yvonne Döring, Danielle S. Perley, François Lefebvre, , Daniel Taliun
WEGS combines low-depth whole genome and high-depth whole exome sequencing to reduce costs while maintaining variant detection accuracy in genetic studies.
npj Genomic Medicine · Feb 7, 2024Peer-reviewedGenomics