16 dependents
| Package | Description | Downloads/month |
|---|---|---|
| Polygenic score toolkit | 8K | |
| Annotate models of genetic inheritance patterns in variant files (vcf files) | 4K | |
| Structural variant toolkit for VCFs | 3K | |
| HiNT -- HiC for copy number vairations and translocations detection | 1K | |
| A collection of software to work with genomic variants | 1K | |
| munger for GWAS summary statistics. | 1K | |
| Forensic analysis tool useful in backwards computing information from next-gener... | 653 | |
| Identify signals of positive selection in somatic mutations | 651 | |
| a framework for training sequence-level deep learning networks | 563 | |
| Category-wide association study (CWAS) (Werling et al., 2018; An et al., 2018) | 555 | |
| Exonic Part centered allele-specific splicing analysis | 513 | |
| A computational approach for identifying cancer driver genes by detecting three-... | 469 | |
| Calculated coverage metrics from a GATK3 Depth Of Coverage file and a bedfile | 237 | |
| himut: single molecule somatic single-base substitution detection using PacBio C... | 137 | |
| scMagnify is a versatile Python toolkit for inferring and analyzing gene regulat... | 71 | |
| Exo-C Data Quality Check, Mapping, and Variant Calling, part of ExoClasma Suite | 43 |
