TY - GEN
T1 - A rule-based expert system for automatic implementation of somatic variant clinical interpretation guidelines
AU - Nicora, Giovanna
AU - Limongelli, Ivan
AU - Cova, Riccardo
AU - Della Porta, Matteo Giovanni
AU - Malcovati, Luca
AU - Cazzola, Mario
AU - Bellazzi, Riccardo
PY - 2019/1/1
Y1 - 2019/1/1
N2 - Precision oncology aims at integrating molecular data into clinical decision making, in order to provide the most suitable therapy and follow-up according to patient’s specific characteristics. A critical step towards this goal is the interpretation of genomic variants, whose presence can be revealed by next generation sequencing. In particular, cancer variant interpretation defines whether the patient harbors genomic alterations that could be targeted by specific drugs, or that were observed as prognostic biomarkers. To standardize somatic interpretation, in 2017 guidelines have been proposed by a working group of associations, including the American Society of Clinical Oncology (ASCO). Automatic tools implementing such guidelines to ease their actual application in the clinical routine are needed. We developed a Rule-based Expert System (ES) that automatically implements ASCO guidelines. ES is an Artificial Intelligence system able to reason over a set of rules and to perform classification, thus emulating human reasoning process. First, we developed automatic pipelines to extract information of over 1500 known diagnostic/prognostic/diagnostic biomarkers from six public databases, including COSMIC and CiVIC. The collected knowledge base is structured in an object-oriented model and the ES is implemented in a Python program through the PyKnow library.
AB - Precision oncology aims at integrating molecular data into clinical decision making, in order to provide the most suitable therapy and follow-up according to patient’s specific characteristics. A critical step towards this goal is the interpretation of genomic variants, whose presence can be revealed by next generation sequencing. In particular, cancer variant interpretation defines whether the patient harbors genomic alterations that could be targeted by specific drugs, or that were observed as prognostic biomarkers. To standardize somatic interpretation, in 2017 guidelines have been proposed by a working group of associations, including the American Society of Clinical Oncology (ASCO). Automatic tools implementing such guidelines to ease their actual application in the clinical routine are needed. We developed a Rule-based Expert System (ES) that automatically implements ASCO guidelines. ES is an Artificial Intelligence system able to reason over a set of rules and to perform classification, thus emulating human reasoning process. First, we developed automatic pipelines to extract information of over 1500 known diagnostic/prognostic/diagnostic biomarkers from six public databases, including COSMIC and CiVIC. The collected knowledge base is structured in an object-oriented model and the ES is implemented in a Python program through the PyKnow library.
KW - Expert System
KW - Somatic variant interpretation
KW - Standard guidelines
UR - http://www.scopus.com/inward/record.url?scp=85068344978&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85068344978&partnerID=8YFLogxK
U2 - 10.1007/978-3-030-21642-9_15
DO - 10.1007/978-3-030-21642-9_15
M3 - Conference contribution
AN - SCOPUS:85068344978
SN - 9783030216412
T3 - Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics)
SP - 114
EP - 119
BT - Artificial Intelligence in Medicine - 17th Conference on Artificial Intelligence in Medicine, AIME 2019, Proceedings
A2 - Wilk, Szymon
A2 - ten Teije, Annette
A2 - Riaño, David
PB - Springer Verlag
T2 - 17th Conference on Artificial Intelligence in Medicine, AIME 2019
Y2 - 26 June 2019 through 29 June 2019
ER -