flashfm-ivis

flashfm-ivis visualizes and compares fine-mapping results to identify potential causal genetic variants across single- and multi-trait quantitative trait analyses.


Key Features:

  • Interactive visualization plots: Provides interactive plots for exploring variant-level fine-mapping results across multiple traits.
  • Network diagrams: Generates network diagrams that illustrate joint effects between variants across different traits.
  • Regional association plots: Integrates fine-mapping results into regional association plots to display variant associations within specific genomic regions.
  • Single- and multi-trait comparison: Compares outputs from single-trait and multi-trait fine-mapping analyses to identify shared or distinct causal variants.

Scientific Applications:

  • Fine-mapping of quantitative traits: Supports localization of putative causal variants underlying variation in quantitative traits.
  • Comparative trait analysis: Enables identification of shared genetic influences and trait-specific associations through comparison of single- and multi-trait results.

Methodology:

Compares single-trait and multi-trait fine-mapping outputs, constructs network diagrams of joint variant effects across traits, and overlays fine-mapping results on regional association plots.

Topics

Details

License:
MIT
Cost:
Free of charge
Tool Type:
web application
Operating Systems:
Mac, Windows, Linux
Programming Languages:
R
Added:
10/2/2022
Last Updated:
11/24/2024

Operations

Publications

Zhou F, Butterworth AS, Asimit JL. <i>Flashfm-ivis</i> : interactive visualization for fine-mapping of multiple quantitative traits. Bioinformatics. 2022;38(17):4238-4242. doi:10.1093/bioinformatics/btac453. PMID:35792838. PMCID:PMC9438951.

PMID: 35792838
PMCID: PMC9438951
Funding: - UK Medical Research Council: MR/L003120/1, MR/R021368/1 - Alan Turing Institute and British Heart Foundation: SP/18/5/33804 - NIHR Blood and Transplant Research Unit in Donor Health and Genomics: NIHR BTRU-2014-10024 - British Heart Foundation: RG/13/13/30194, RG/18/13/33946, SP/09/002 - NIHR Cambridge BRC: BRC-1215-20014

Links