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Feliubadalo, L.

Publications and source records attributed to Feliubadalo, L..

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Choosing variant interpretation tools for clinical applications: context matters

Our inability to solve the Variant Interpretation Problem (VIP) has become a bottleneck in the biomedical/clinical application of Next-Generation Sequencing. This situation has favored the development and use of bioinformatics tools for the VIP. However, choosing the optimal tool for our purposes is difficult because of the high variability of clinical contexts across and within countries. Here, we introduce the use of cost models as a new approach to compare pathogenicity predictors that considers clinical context. An interesting feature of this approach, absent in standard performance measures, is that it treats pathogenicity predictors as rejection classifiers. These classifiers, commonly found in machine learning applications to healthcare, reject low-confidence predictions. Finally, to explore whether context has any impact on predictor selection, we have developed a computational procedure that solves the problem of comparing an arbitrary number of tools across all possible clinical scenarios. We illustrate our approach using a set of seventeen pathogenicity predictors for missense variants. Our results show that there is no optimal predictor for all possible clinical scenarios. We also find that considering rejection gives a view of classifiers contrasting with that of standard performance measures. The Python code for comparing pathogenicity predictors across the clinical space using cost models is available to any interested user at: https://github.com/ClinicalTranslationalBioinformatics/clinical_space_partition SummariesJosu Aguirre earned his doctorate at the Clinical and Translational Bioinformatics group, at the Vall dHebron Institute of Research (VHIR). Natalia Padilla earned is a post-doctoral researcher at the Clinical and Translational Bioinformatics group, at the Vall dHebron Institute of Research (VHIR). Selen Ozkan is a Ph.D. student at the Clinical and Translational Bioinformatics group, at the Vall dHebron Institute of Research (VHIR). Casandra Riera earned her doctorate at the Clinical and Translational Bioinformatics group, at the Vall dHebron Institute of Research (VHIR). Lidia Feliubadalo earned her doctorate at the Universitat de Barcelona, presently she is a high-level technician working at the Catalan Institute of Oncology (ICO) in the diagnosis of hereditary cancers. Xavier de la Cruz is ICREA Research Professor at the Vall dHebron Institute of Research (VHIR). His research interests revolve around the application of machine learning methods to healthcare problems.

bioinformatics↗

Benchmark of tools for CNV detection from NGS panel data in a genetic diagnostics context

MotivationAlthough germline copy number variants (CNVs) are the genetic cause of multiple hereditary diseases, detecting them from targeted next-generation sequencing data (NGS) remains a challenge. Existing tools perform well for large CNVs but struggle with single and multi-exon alterations. The aim of this work is to evaluate CNV calling tools working on gene panel NGS data with CNVs up to single-exon resolution and their suitability as a screening step before orthogonal confirmation in genetic diagnostics strategies. ResultsFive tools (DECoN, CoNVaDING, panelcn.MOPS, ExomeDepth and CODEX2) were tested against four genetic diagnostics datasets (495 samples, 231 CNVs), using the default and sensitivity-optimized parameters. Most tools were highly sensitive and specific, but the performance was dataset-dependant. In our in-house datasets, DECoN and panelcn.MOPS with optimized parameters showed enough sensitivity to be used as screening methods in genetic diagnostics. AvailabilityBenchmarking-optimization code is freely available at https://github.com/TranslationalBioinformaticsIGTP/CNVbenchmarkeR.

bioinformatics↗