16 dependents
| Package | Description | Downloads/month |
|---|---|---|
| GA4GH Categorical Variation Representation Python Implementation | 307K | |
| GA4GH Variation Annotation Python Implementation | 303K | |
| Services and guidelines for normalizing genes | 8K | |
| Common Operation on Lots of Sequences Tool | 6K | |
| Services and guidelines for normalizing disease terms | 4K | |
| VICC normalization routine for variations | 4K | |
| Hail helper functions for the gnomAD project and Translational Genomics Group | 4K | |
| CIViC variant knowledgebase analysis toolkit. | 4K | |
| Services and guidelines for normalizing drug and other therapy terms | 3K | |
| Computable object representation and validation for gene fusions | 3K | |
| A search interface for cancer variant interpretations assembled by aggregating a... | 549 | |
| Lightweight, portable variation registration and retrieval | 475 | |
| Extract clinical variant interpretations from VCF using GA4GH VRS IDs | 399 | |
| Map MaveDB scoresets to VRS objects | 274 | |
| Lightweight, portable variation registration and retrieval | 182 | |
| Extract clinical variant interpretations from VCF using GA4GH VRS IDs | 59 |
