Kimimila: A New Model to Classify NGS Short Reads by Their Allele Origin. - Andrea Marinoni; Ettore Rizzo; Paolo Gamba; Riccardo Bellazzi; Ivan Limongelli (ICHI, 2014)

A Genomic Data Fusion Framework to Exploit Rare and Common Variants for Association Discovery. - Simone Marini; Ivan Limongelli; Ettore Rizzo; Tan Da; Riccardo Bellazzi (AIME, 2015)

BigQ: a NoSQL based framework to handle genomic variants in i2b2. - Matteo Gabetta; Ivan Limongelli; Ettore Rizzo; Alberto Riva; Daniele Segagni; Riccardo Bellazzi (BMC Bioinform., 2015)

PaPI: pseudo amino acid composition to score human protein-coding variants. - Ivan Limongelli; Simone Marini; Riccardo Bellazzi (BMC Bioinform., 2015)

A kinetic model-based algorithm to classify NGS short reads by their allele origin. - Andrea Marinoni; Ettore Rizzo; Ivan Limongelli; Paolo Gamba; Riccardo Bellazzi (J. Biomed. Informatics, 2015)

Big Data as a Driver for Clinical Decision Support Systems: A Learning Health Systems Perspective. - Arianna Dagliati; Valentina Tibollo; Lucia Sacchi; Alberto Malovini; Ivan Limongelli; Matteo Gabetta; Carlo Napolitano; Andrea Mazzanti; Pasquale De Cata; Luca Chiovato; Silvia G. Priori; Riccardo Bellazzi (Frontiers Digit. Humanit., 2018)

A Rule-Based Expert System for Automatic Implementation of Somatic Variant Clinical Interpretation Guidelines. - Giovanna Nicora; Ivan Limongelli; Riccardo Cova; Matteo Giovanni Della Porta; Luca Malcovati; Mario Cazzola; Riccardo Bellazzi (AIME, 2019)

A Semi-supervised Learning Approach for Pan-Cancer Somatic Genomic Variant Classification. - Giovanna Nicora; Simone Marini; Ivan Limongelli; Ettore Rizzo; Stefano Montoli; Francesca Floriana Tricomi; Riccardo Bellazzi (AIME, 2019)