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Costa, B. M.

Publications and source records attributed to Costa, B. M..

2 recordsLinked to original sources

A Novel Tool for Multi-Omics Network Integration and Visualization: A Study of Glioma Heterogeneity

Gliomas are highly heterogeneous tumors with generally poor prognoses. Leveraging multi-omics data and network analysis holds great promise in uncovering crucial signatures and molecular relationships that elucidate glioma heterogeneity. However, the complexity of the problem and the high dimensionality of the data increase the challenges of integrating information across various biological levels. In this study, we developed a framework comprising two steps for variable selection based on sparse network estimation from various omics. Subsequently, we introduced MINGLE (Multi-omics Integrated Network for GraphicaL Exploration), a novel methodology designed to merge distinct multi-omics information into a single network, enabling the identification of underlying relations through an innovative integrated visualization. Applying this method to glioma data, with patients grouped according to the newest glioma classification guidelines, led to the selection of variables as potential candidates for novel glioma-type-specific biomarkers.

bioinformatics↗

Updating TCGA glioma classification through integration of molecular profiling data following the 2016 and 2021 WHO guidelines

The understanding of glioma disease has been evolving drastically with dedicated research into the genetic and molecular profiling of glioma tumour tissue. Molecular biomarkers have gained progressive and substantial importance in providing diagnostic information, leading to groundbreaking changes in the tumour classification system, criteria and taxonomy standardised by the 2016 and 2021 editions of the World Health Organization Classification of Tumours of the Central Nervous Systems guidelines (WHO-2016 and WHO-2021, respectively). Some of the insights into glioma disease derived from extensive research on open-source multi-omics databases, such as the Cancer Genome Atlas (TCGA). However, given the substantial changes in glioma classification, retrospective databases may harbour outdated diagnostic annotations, suboptimal for further research. Here we propose two methods for updating the tumour classification of TCGA glioma samples in accordance with WHO-2016 and WHO-2021 guidelines through the integration of curated molecular profiling information. Our methods allowed for the diagnostic update of 98% and 87% of evaluated TCGA glioma cases according to WHO-2016 and -2021, respectively, and highlighted changes in patient-specific diagnosis across both guidelines editions. Our reclassification pipelines are provided in software R, facilitating direct reproduction or tailoring upon new releases of WHO guidelines.

bioinformatics↗