Ettore Rizzo

A Genomic Data Fusion Framework to Exploit Rare and Common Variants for Association Discovery

Riccardo Bellazzi, Simone Marini, Ivan Limongelli, 2015, AIME.

Scalable and cost-effective NGS genotyping in the cloud

Peter J. Tonellato, Yassine Souilmi, Hassan Ghazal, 2015, BMC Medical Genomics.

Kimimila: A New Model to Classify NGS Short Reads by Their Allele Origin

Paolo Gamba, Riccardo Bellazzi, Andrea Marinoni, 2014, ICHI.

A Semi-supervised Learning Approach for Pan-Cancer Somatic Genomic Variant Classification

Riccardo Bellazzi, Simone Marini, Ivan Limongelli, 2019, AIME.

BigQ: a NoSQL based framework to handle genomic variants in i2b2

Alberto Riva, Riccardo Bellazzi, Matteo Gabetta, 2015, BMC Bioinformatics.

A kinetic model-based algorithm to classify NGS short reads by their allele origin

Paolo Gamba, Riccardo Bellazzi, Andrea Marinoni, 2015, J. Biomed. Informatics.

Additional file 6: Table S4. of Scalable and cost-effective NGS genotyping in the cloud

Peter J. Tonellato, Yassine Souilmi, Jae-Yoon Jung, 2015 .

A Data Fusion Approach to Enhance Association Study in Epilepsy

Riccardo Bellazzi, Alberto Malovini, Ivan Limongelli, 2016, PloS one.