Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios. - Johan Staaf; Johan Vallon-Christersson; David Lindgren; Gunnar Juliusson; Richard Rosenquist; Mattias Höglund; Åke Borg; Markus Ringnér (BMC Bioinform., 2008)

AEGLE: A big bio-data analytics framework for integrated health-care services. - Dimitrios Soudris; Sotirios Xydis; Christos Baloukas; Anastasia Hadzidimitriou; Ioanna Chouvarda; Kostas Stamatopoulos; Nicos Maglaveras; John Chang; Andreas Raptopoulos; David Manset; Barbara K. Pierscionek; Reem Kayyali; et al. (SAMOS, 2015)

Automated shape-based clustering of 3D immunoglobulin protein structures in chronic lymphocytic leukemia. - Eleftheria Polychronidou; Ilias Kalamaras; Andreas Agathangelidis; Lesley Ann Sutton; Xiao-Jie Yan; Vasilis Bikos; Anna Vardi; Konstantinos Mochament; Nicholas Chiorazzi; Chrysoula Belessi; Richard Rosenquist; Paolo Ghia; et al. (BMC Bioinform., 2018)

Using Electronic Patient Reported Outcomes to Foster Palliative Cancer Care: The MyPal Approach. - Christos Maramis; Sheila Payne; Sarka Pospisilova; Richard Rosenquist; Paolo Ghia; Charalampos Pontikoglou; Annette Sander; Michael Doubek; Norbert M. Graf; Julie Ling; Julia Downing; Christina Karamanidou; et al. (BIBE, 2019)

Smart variant filtering - A blueprint solution for massively parallel sequencing-based variant analysis. - Orlinda Brahimllari; Sandra Eloranta; Patrik Georgii-Hemming; Zahra Haider; Sabine Koch; Aleksandra Krstic; Frantzeska Papadopoulou Skarp; Richard Rosenquist; Karin E. Smedby; Fulya Taylan; Birna Thorvaldsdottir; Valtteri Wirta; et al. (Health Informatics J., 2024)