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De Bortoli, M.

Publications and source records attributed to De Bortoli, M..

2 recordsLinked to original sources

DoAggregate: a pipeline for aggregation testing for rare-variant on a gene and pathway level

Motivation Aggregation tests overcome the classical limitation of rare variant analysis in cohort study design. Choosing the right statistical test remains one of the biggest challenges. Existing tools fall short in offering a comprehensive solution that includes automatic data processing, testing across all genes, as well as exploration of broader genetic regions such as pathways and Gene Ontology (GO) terms. Most aggregation tests only report p-values and basic statistics, lacking in the presentation of cohort level statistics and comparison of results across whole genome or exome scales. Results We introduce DoAggregate, an innovative, scalable pipeline designed to address these challenges. DoAggregate enables users to perform aggregation tests across genes, pathways, and GO terms. It leverages Excalibur, an ensemble approach combining 36 distinct aggregation methods. The pipeline enhances data analysis by presenting over-representation analysis and aggregation results in detailed Excel sheets, complete with annotations and plots to facilitate nuanced interpretation and comparison. Applied to public exome data from the 1000 Genomes Project, DoAggregate tested 10,447 genes, 49 over-represented pathways and 36 over-represented GO terms in a single run, returning annotated, cohort-level results for each region. Availability and implementation DoAggregate source code, documentation and installation instructions as well as test data sets and results are freely available at https://github.com/boutrys/DoAggregate and released under the MIT license. The repository contains the serial implementation (R package), the parallel implementation for Slurm-based computer clusters and the web application.

bioinformatics↗

KCND3 is a novel susceptibility locus for early repolarization

The presence of an early repolarization pattern (ERP) on the surface electrocardiogram (ECG) is associated with risk of ventricular fibrillation and sudden cardiac death. Family studies have shown that ERP is a highly heritable trait but molecular genetic determinants are unknown. We assessed the ERP in 12-lead ECGs of 39,456 individuals and conducted a two-stage meta-analysis of genome-wide association studies (GWAS). In the discovery phase, we included 2,181 cases and 23,641 controls from eight European ancestry studies and identified 19 genome-wide significant (p<5E-8) variants in the KCND3 (potassium voltage gated channel subfamily D member 3) gene with a p-value of 4.6E-10. Replication of two loci in four additional studies including 1,124 cases and 12,510 controls confirmed the association at the KCND3 gene locus with a pooled odds ratio of 0.82, p=7.7E-12 (rs1545300 minor allele T). A subsequent GWAS meta-analysis combining all samples did not reveal additional loci. The lead SNP of the discovery stage (rs12090194) was in strong linkage disequilibrium with rs1545300 (r2=0.96, D=1). Summary statistics based conditional analysis did not reveal any secondary signals. Co-localization analyses indicate causal effects of KCND3 gene expression levels on ERP in both the left ventricle of the heart and in tibial artery.\n\nIn this study we identified for the first time a genome-wide significant association of a genetic variant with ERP. Our findings of a locus in the KCND3 gene not only provide insights into the genetic determinants but also into the pathophysiological mechanism of ERP, revealing a promising candidate for functional studies.

genetics↗