19 dependents
| Package | Description | Downloads/month |
|---|---|---|
| Library for manipulating genomic variants and predicting their effects | 58K | |
| Copy Number Variant Pathogenicity Classifier | 6K | |
| OpenCRAVAT - variant analysis toolkit | 1K | |
| Automated DNA micro-satellite genotyping | 963 | |
| Python package to calculate various sample contamination metrics. | 765 | |
| Python package to query cancer variant databases | 679 | |
| This hosts multiple scripts necessary for filtering and processing of variant ca... | 486 | |
| 411 | ||
| Generate and store genetic data into an Elasticsearch database. | 401 | |
| Package that creates data files for CGAP's Higlass browsers | 372 | |
| Workflow for whole genome sequencing based phylogeny of Illumina and ONT data. | 312 | |
| Long-read-based human genomic structural variation detection with cuteSVTrio | 245 | |
| primer design for haplotype genotyping using indel information | 170 | |
| Bio-Wrangler is a Python package for bioinformatics data wrangling. It helps loa... | 132 | |
| command line and desktop tool for microbial variant calling | 95 | |
| Highly Open Workflow for Annotation & Ranking toward genomic variant Discovery | 77 | |
| Highly Open Workflow for Annotation & Ranking toward genomic variant Discovery | 69 | |
| The Evolutionary Bio-Compiler: A living engine for programming biology through e... | 64 | |
| 7 |
