VCF to CSV Converter
Converts VCF variant data to CSV, enabling researchers and analysts to inspect, filter, and export variant information in spreadsheets.
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About This Tool
Under the hood, the tool uses a robust streaming parser to handle large VCF files without loading them entirely into memory. It validates VCF syntax, normalizes numeric values, and ensures proper CSV quoting. When expanding INFO, parses key=value pairs and places them into dedicated columns if selected. If sample data expansion is enabled, FORMAT/sample fields can be surfaced as separate columns or omitted for a compact table. Output delimiter can be set to comma or tab for TSV compatibility. The converter also preserves header lines from the VCF file (starting with #) when exporting to CSV, so downstream processes retain context.
Target users include genomics researchers, clinical diagnostics teams, data engineers, and bioinformaticians who need to integrate variant data into reports, dashboards, or pipelines. Unique value drivers include dual input modes (upload or paste), flexible INFO expansion, controlled multi-allelic handling, and streaming processing that scales to large files. The tool emphasizes data integrity by producing well-formed CSV, gracefully handling errors, and preserving header information for reproducibility.
How to Use
- Provide inputs by uploading a VCF file or pasting VCF text.
- Select options: split multi-allelic ALT into separate rows; expand INFO keys into separate columns; expand FORMAT/SAMPLE fields; choose delimiter.
- Run conversion to generate CSV output.
- Review the CSV result in preview and download.
- Validate a subset of rows; use the exported CSV in downstream analysis.
Frequently Asked Questions
Find Quick Answers
What input formats are supported?
Can I expand INFO fields?
How are multi-allelic records handled?
Is there a performance limit for large VCF files?
Need to run multiple calculations?
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