VIVID: A Web Application for Variant Interpretation and Visualization in Multi-dimensional Analyses.
Swapnil TichkuleYoochan MyungMyo T NaungBrendan R E AnsellAndrew J GuyNamrata SrivastavaSomya MehraSimone M CacciòIvo MuellerAlyssa E BarryCock Van OosterhoutBernard J PopeDavid Benjamin AscherAaron R JexPublished in: Molecular biology and evolution (2022)
Large-scale comparative genomics- and population genetic studies generate enormous amounts of polymorphism data in the form of DNA variants. Ultimately, the goal of many of these studies is to associate genetic variants to phenotypes or fitness. We introduce VIVID, an interactive, user-friendly web application that integrates a wide range of approaches for encoding genotypic to phenotypic information in any organism or disease, from an individual or population, in three-dimensional (3D) space. It allows mutation mapping and annotation, calculation of interactions and conservation scores, prediction of harmful effects, analysis of diversity and selection, and 3D visualization of genotypic information encoded in Variant Call Format on AlphaFold2 protein models. VIVID enables the rapid assessment of genes of interest in the study of adaptive evolution and the genetic load, and it helps prioritizing targets for experimental validation. We demonstrate the utility of VIVID by exploring the evolutionary genetics of the parasitic protist Plasmodium falciparum, revealing geographic variation in the signature of balancing selection in potential targets of functional antibodies.
Keyphrases
- genome wide
- plasmodium falciparum
- copy number
- case control
- dna methylation
- health information
- high resolution
- electronic health record
- physical activity
- cell free
- social media
- healthcare
- machine learning
- climate change
- rna seq
- risk assessment
- data analysis
- mass spectrometry
- binding protein
- loop mediated isothermal amplification
- sensitive detection
- genome wide identification