De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data

by Adam Ameur, Huiwen Che, Marcel Martin, Ignas Bunikis, Johan Dahlberg, Ida Höijer, Susana Häggqvist, Francesco Vezzi, Jessica Nordlund, Pall Olason, Lars Feuk, Ulf Gyllensten
Published 2018-10-01

Comprehensive genome-wide analysis of routine non-invasive test data allows cancer prediction: A single-center retrospective analysis of over 85,000 pregnancies

by Liesbeth Lenaerts, PhD, Nathalie Brison, PhD, Charlotte Maggen, MD, Leen Vancoillie, PhD, Huiwen Che, MsC, Peter Vandenberghe, MD, PhD, Daan Dierickx, MD, PhD, Lucienne Michaux, MD, Phd, Barbara Dewaele, PhD, Patrick Neven, MD, PhD, Giuseppe Floris, MD, PhD, Thomas Tousseyn, MD, PhD, Lore Lannoo, MD, Tatjana Jatsenko, PhD, Isabelle Vanden Bempt, PhD, Kristel Van Calsteren, MD, PhD, Vincent Vandecaveye, MD, PhD, Luc Dehaspe, PhD, Koenraad Devriendt, MD, PhD, Eric Legius, MD, PhD, Kris Van Den Bogaert, PhD, Joris Robert Vermeesch, PhD, Frédéric Amant, MD, PhD
Published 2021-05-01