Abstract

EcholocatoR integrates a diverse suite of statistical and functional fine-mapping tools to identify, test enrichment in, and visualize high-confidence causal consensus variants in any phenotype. It requires minimal input from users (a summary statistics file), can be run in a single R function, and provides extensive access to relevant datasets (e.g. reference linkage disequilibrium panels, quantitative trait loci, genome-wide annotations, cell-type-specific epigenomics), thereby enabling rapid, robust and scalable end-to-end fine-mapping investigations.

Original languageEnglish
Pages (from-to)536-539
Number of pages4
JournalBioinformatics
Volume38
Issue number2
DOIs
StatePublished - 15 Jan 2022

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