Copying and storing genomic variants
Copy and store raw VCF files in Cloud Storage.
Loading and transforming genomic variants
Load and transform VCF files into BigQuery for large-scale analysis.
Handling large inputs
Learn how to improve performance and reduce costs when loading large numbers of files.
Validating VCF files with the preprocessor tool
Use the Variant Transforms tool VCF files preprocessor to validate VCF files.
Parsing and annotating VCF files
Use the annotation support available in the Variant Transforms tool.
Understanding the BigQuery variants table schema
Use the Cloud Life Sciences API to export variants to BigQuery.
Flattening the BigQuery variants table
Flatten the BigQuery variants table to remove repeated records.
Troubleshooting the variant transforms tool
Get solutions to common problems.