Article

ExonViz: A user friendly application to visualize transcripts and genetic variants

2024-09-20

Abstract excerpt

Visualization of genes and genetic variants as well as transcript structure is essential within the human genetics community. Such illustrations represent a key tool in communicating genetic concepts and facilitating discussions on therapeutic interventions. There currently are no easily usable tools which allows the users to draw all features required for a comprehensive overview of a transcript’s structure and t...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 0ca33ff9-ff90-520b-81b9-6654d39a8ca4
DOI: 10.1101/2024.09.18.24313945

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

ExonViz: A user friendly application to visualize transcripts and genetic variantsDOI 10.1101/2024.09.18.24313945Read

GPViz: dynamic visualization of genomic regions and variants affecting protein domains.Semantic proximity Read

VisVariant: A java program to visualise genetic variants in next-generation sequencing dataSemantic proximity Read

Complex structural variant visualization with SVTopoSemantic proximity Read

Advancing clinical genomics and precision medicine with GVViZ: FAIR bioinformatics platform for variable gene-disease annotation, visualization, and expression analysis.Semantic proximity Read

igv-reports: embedding interactive genomic visualizations in HTML reports to aid variant review.Semantic proximity Read

BioJS-HGV Viewer: Genetic Variation VisualizerSemantic proximity Read

MitoVisualize: A resource for analysis of variants in human mitochondrial RNAs and DNASemantic proximity Read

Slinker: Visualising novel splicing events in RNA-Seq dataSemantic proximity Read

DoChaP: The Domain Change PresenterSemantic proximity Read

CoMut: Visualizing integrated molecular information with comutation plotsSemantic proximity Read

Visualization tools for human structural variations identified by whole-genome sequencing.Semantic proximity Read

RareVariantVis: new tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing data.Semantic proximity Read