TY - JOUR
T1 - Covering Hierarchical Dirichlet Mixture Models on binary data to enhance genomic stratifications in onco-hematology
AU - Dall’Olio, Daniele
AU - Sträng, Eric
AU - Turki, Amin T.
AU - Tettero, Jesse M.
AU - Barbus, Martje
AU - Schulze-Rath, Renate
AU - Elicegui, Javier Martinez
AU - Matteuzzi, Tommaso
AU - Merlotti, Alessandra
AU - Carota, Luciana
AU - Sala, Claudia
AU - Della Porta, Matteo G.
AU - Giampieri, Enrico
AU - HARMONY Healthcare Alliance Consortium
AU - Hernández-Rivas, Jesús María
AU - Bullinger, Lars
AU - Castellani, Gastone
N1 - Publisher Copyright: © 2024 Dall’Olio et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2024/2/1
Y1 - 2024/2/1
N2 - Onco-hematological studies are increasingly adopting statistical mixture models to support the advancement of the genomically-driven classification systems for blood cancer. Targeting enhanced patients stratification based on the sole role of molecular biology attracted much interest and contributes to bring personalized medicine closer to reality. In onco-hematology, Hierarchical Dirichlet Mixture Models (HDMM) have become one of the preferred method to cluster the genomics data, that include the presence or absence of gene mutations and cytogenetics anomalies, into components. This work unfolds the standard workflow used in onco-hematology to improve patient stratification and proposes alternative approaches to characterize the components and to assign patient to them, as they are crucial tasks usually supported by a priori clinical knowledge. We propose (a) to compute the parameters of the multinomial components of the HDMM or (b) to estimate the parameters of the HDMM components as if they were Multivariate Fisher’s Non-Central Hypergeometric (MFNCH) distributions. Then, our approach to perform patients assignments to the HDMM components is designed to essentially determine for each patient its most likely component. We show on simulated data that the patients assignment using the MFNCH-based approach can be superior, if not comparable, to using the multinomial-based approach. Lastly, we illustrate on real Acute Myeloid Leukemia data how the utilization of MFNCH-based approach emerges as a good trade-off between the rigorous multinomial-based characterization of the HDMM components and the common refinement of them based on a priori clinical knowledge.
AB - Onco-hematological studies are increasingly adopting statistical mixture models to support the advancement of the genomically-driven classification systems for blood cancer. Targeting enhanced patients stratification based on the sole role of molecular biology attracted much interest and contributes to bring personalized medicine closer to reality. In onco-hematology, Hierarchical Dirichlet Mixture Models (HDMM) have become one of the preferred method to cluster the genomics data, that include the presence or absence of gene mutations and cytogenetics anomalies, into components. This work unfolds the standard workflow used in onco-hematology to improve patient stratification and proposes alternative approaches to characterize the components and to assign patient to them, as they are crucial tasks usually supported by a priori clinical knowledge. We propose (a) to compute the parameters of the multinomial components of the HDMM or (b) to estimate the parameters of the HDMM components as if they were Multivariate Fisher’s Non-Central Hypergeometric (MFNCH) distributions. Then, our approach to perform patients assignments to the HDMM components is designed to essentially determine for each patient its most likely component. We show on simulated data that the patients assignment using the MFNCH-based approach can be superior, if not comparable, to using the multinomial-based approach. Lastly, we illustrate on real Acute Myeloid Leukemia data how the utilization of MFNCH-based approach emerges as a good trade-off between the rigorous multinomial-based characterization of the HDMM components and the common refinement of them based on a priori clinical knowledge.
UR - http://www.scopus.com/inward/record.url?scp=85185721160&partnerID=8YFLogxK
U2 - 10.1371/journal.pcbi.1011299
DO - 10.1371/journal.pcbi.1011299
M3 - Article
C2 - 38306404
SN - 1553-734X
VL - 20
JO - PLoS computational biology
JF - PLoS computational biology
IS - 2
M1 - e1011299
ER -