Tools for Human Genome Variant Interpretation
Start with a concrete GeneBe use case, then choose the workflow that fits your data and tools.
Concrete use cases for annotating variants, working with files, and automating GeneBe.
Learn how to search variants, understand accepted formats, and use ACMG results.
Upload VCF, FASTQ, or BAM data and prepare a report for your analysis.
Browse and filter local VCF and BED files without uploading them to a server.
Use the API, Python, or the command-line client in your own workflow.
Use, create, and manage local variant annotation databases.
Review genome builds, file formats, and variant representation.