XVCF: Exquisite Visualization of VCF Data from Genomic Experiments

Abstract excerpt

<h4>Background</h4> High-throughput genomic analyses of germline and cancer genomes facilitate the identification of causal and actionable genetic variants. The recent advances in next-generation sequencing technology generated large-scale genomic and/or multi-omics datasets from different disease types or models. Owing to the huge volume of data coming out of genomic experiments, scientists are facing challenges...

Topics

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• Computational Biology
• Computer Graphics
• Genetic Variation
• Genomics
• High-Throughput Nucleotide Sequencing
• Polymorphism, Single Nucleotide
• Software
• User-Computer Interface

Identifiers and source

Literature Corpus work

40a98b6d-eb25-5898-8fec-ee48b12710fb

DOI

10.1101/2025.04.30.651450