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Ettore Rizzo

Showing results (1-10 of 28) with videos related to

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Journal of Biomedical Informatics|October 15, 2014
A kinetic model-based algorithm to classify NGS short reads by their allele originAndrea Marinoni, Ettore Rizzo, Ivan Limongelli, et al.
Bioinformatics (Oxford, England)|April 5, 2024
VarChat: the generative AI assistant for the interpretation of human genomic variationsFederica De Paoli, Silvia Berardelli, Ivan Limongelli, et al.
BMC Bioinformatics|December 31, 2015
BigQ: a NoSQL based framework to handle genomic variants in i2b2Matteo Gabetta, Ivan Limongelli, Ettore Rizzo, et al.
Plos One|December 17, 2016
A Data Fusion Approach to Enhance Association Study in EpilepsySimone Marini, Ivan Limongelli, Ettore Rizzo, et al.
NAR Genomics and Bioinformatics|March 31, 2025
Digenic variant interpretation with hypothesis-driven explainable AIFederica De Paoli, Giovanna Nicora, Silvia Berardelli, et al.
BMC Genomics|July 6, 2017
Comparative genomics shows that viral integrations are abundant and express piRNAs in the arboviral vectors Aedes aegypti and Aedes albopictusUmberto Palatini, Pascal Miesen, Rebeca Carballar-Lejarazu, et al.
American Journal of Hematology|September 10, 2025
CHEK2 Germline Variants in Early-Onset and Familial Myeloproliferative NeoplasmsOscar Borsani, Elisabetta Molteni, Daniela Pietra, et al.
BMC Medical Genomics|October 17, 2015
Scalable and cost-effective NGS genotyping in the cloudYassine Souilmi, Alex K Lancaster, Jae-Yoon Jung, et al.
Haematologica|October 7, 2017
Pattern of somatic mutations in patients with Waldenström macroglobulinemia or IgM monoclonal gammopathy of undetermined significanceMarzia Varettoni, Silvia Zibellini, Irene Defrancesco, et al.
Blood|May 22, 2023
Prevalence and clinical expression of germ line predisposition to myeloid neoplasms in adults with marrow hypocellularityElisabetta Molteni, Elisa Bono, Anna Gallì, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
Journal of Biomedical Informatics|October 15, 2014
A kinetic model-based algorithm to classify NGS short reads by their allele originAndrea Marinoni, Ettore Rizzo, Ivan Limongelli, et al.
Bioinformatics (Oxford, England)|April 5, 2024
VarChat: the generative AI assistant for the interpretation of human genomic variationsFederica De Paoli, Silvia Berardelli, Ivan Limongelli, et al.
BMC Bioinformatics|December 31, 2015
BigQ: a NoSQL based framework to handle genomic variants in i2b2Matteo Gabetta, Ivan Limongelli, Ettore Rizzo, et al.
Plos One|December 17, 2016
A Data Fusion Approach to Enhance Association Study in EpilepsySimone Marini, Ivan Limongelli, Ettore Rizzo, et al.
NAR Genomics and Bioinformatics|March 31, 2025
Digenic variant interpretation with hypothesis-driven explainable AIFederica De Paoli, Giovanna Nicora, Silvia Berardelli, et al.
BMC Genomics|July 6, 2017
Comparative genomics shows that viral integrations are abundant and express piRNAs in the arboviral vectors Aedes aegypti and Aedes albopictusUmberto Palatini, Pascal Miesen, Rebeca Carballar-Lejarazu, et al.
American Journal of Hematology|September 10, 2025
CHEK2 Germline Variants in Early-Onset and Familial Myeloproliferative NeoplasmsOscar Borsani, Elisabetta Molteni, Daniela Pietra, et al.
BMC Medical Genomics|October 17, 2015
Scalable and cost-effective NGS genotyping in the cloudYassine Souilmi, Alex K Lancaster, Jae-Yoon Jung, et al.
Haematologica|October 7, 2017
Pattern of somatic mutations in patients with Waldenström macroglobulinemia or IgM monoclonal gammopathy of undetermined significanceMarzia Varettoni, Silvia Zibellini, Irene Defrancesco, et al.
Blood|May 22, 2023
Prevalence and clinical expression of germ line predisposition to myeloid neoplasms in adults with marrow hypocellularityElisabetta Molteni, Elisa Bono, Anna Gallì, et al.
Pageof 3