Ivan Limongelli

Orcid: 0000-0002-9781-2974

According to our database1, Ivan Limongelli authored at least 8 papers between 2014 and 2019.

Collaborative distances:
  • Dijkstra number2 of five.
  • Erdős number3 of four.

Timeline

Legend:

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PhD thesis 
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Links

On csauthors.net:

Bibliography

2019
A Semi-supervised Learning Approach for Pan-Cancer Somatic Genomic Variant Classification.
Proceedings of the Artificial Intelligence in Medicine, 2019

A Rule-Based Expert System for Automatic Implementation of Somatic Variant Clinical Interpretation Guidelines.
Proceedings of the Artificial Intelligence in Medicine, 2019

2018
Big Data as a Driver for Clinical Decision Support Systems: A Learning Health Systems Perspective.
Frontiers Digit. Humanit., 2018

2015
A kinetic model-based algorithm to classify NGS short reads by their allele origin.
J. Biomed. Informatics, 2015

PaPI: pseudo amino acid composition to score human protein-coding variants.
BMC Bioinform., 2015

BigQ: a NoSQL based framework to handle genomic variants in i2b2.
BMC Bioinform., 2015

A Genomic Data Fusion Framework to Exploit Rare and Common Variants for Association Discovery.
Proceedings of the Artificial Intelligence in Medicine, 2015

2014
Kimimila: A New Model to Classify NGS Short Reads by Their Allele Origin.
Proceedings of the 2014 IEEE International Conference on Healthcare Informatics, 2014


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