Model-based clustering is a technique widely used to group a collection of units into mutually exclusive groups. There are, however, situations in which an observation could in principle belong to more than one cluster. In the context of next-generation sequencing (NGS) experiments, for example, the signal observed in the data might be produced by two (or more) different biological processes operating together and a gene could participate in both (or all) of them. We propose a novel approach to cluster NGS discrete data, coming from a ChIP-Seq experiment, with a mixture model, allowing each unit to belong potentially to more than one group: these multiple allocation clusters can be flexibly defined via a function combining the features of the original groups without introducing new parameters. The formulation naturally gives rise to a ‘zero-inflation group’ in which values close to zero can be allocated, acting as a correction for the abundance of zeros that manifest in this type of data. We take into account the spatial dependency between observations, which is described through a latent conditional autoregressive process that can reflect different dependency patterns. We assess the performance of our model within a simulation environment and then we apply it to ChIP-seq real data.

Mixture model with multiple allocations for clustering spatially correlated observations in the analysis of ChIP-Seq data / Ranciati, Saverio; Viroli, Cinzia; Wit, Ernst C.. - In: BIOMETRICAL JOURNAL. - ISSN 0323-3847. - STAMPA. - 59:6(2017), pp. 1301-1316. [10.1002/bimj.201600131]

Mixture model with multiple allocations for clustering spatially correlated observations in the analysis of ChIP-Seq data

RANCIATI, SAVERIO
;
VIROLI, CINZIA;
2017

Abstract

Model-based clustering is a technique widely used to group a collection of units into mutually exclusive groups. There are, however, situations in which an observation could in principle belong to more than one cluster. In the context of next-generation sequencing (NGS) experiments, for example, the signal observed in the data might be produced by two (or more) different biological processes operating together and a gene could participate in both (or all) of them. We propose a novel approach to cluster NGS discrete data, coming from a ChIP-Seq experiment, with a mixture model, allowing each unit to belong potentially to more than one group: these multiple allocation clusters can be flexibly defined via a function combining the features of the original groups without introducing new parameters. The formulation naturally gives rise to a ‘zero-inflation group’ in which values close to zero can be allocated, acting as a correction for the abundance of zeros that manifest in this type of data. We take into account the spatial dependency between observations, which is described through a latent conditional autoregressive process that can reflect different dependency patterns. We assess the performance of our model within a simulation environment and then we apply it to ChIP-seq real data.
2017
Mixture model with multiple allocations for clustering spatially correlated observations in the analysis of ChIP-Seq data / Ranciati, Saverio; Viroli, Cinzia; Wit, Ernst C.. - In: BIOMETRICAL JOURNAL. - ISSN 0323-3847. - STAMPA. - 59:6(2017), pp. 1301-1316. [10.1002/bimj.201600131]
Ranciati, Saverio; Viroli, Cinzia; Wit, Ernst C.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/610660
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