| Name | Version | Summary | date |
| vcfio |
1.2.0 |
A simple and efficient VCF manipulation package. |
2025-07-29 09:58:03 |
| etiennevar |
1.0.4 |
Outil en ligne de commande pour résumer et visualiser les fichiers VCF |
2025-07-09 05:21:47 |
| plink-bed-reader |
1.0.2 |
Lightweight and memory efficient reader for PLINK BED files. It supports both SNP-major and individual-major formats. Written in pure Python. |
2025-02-21 12:29:28 |
| varscore |
0.0.1a0 |
A library for common functions in variant effect prediction & prioritization. |
2025-01-17 23:39:08 |
| biothings-client |
0.4.0 |
Python Client for BioThings API services. |
2025-01-10 22:09:45 |
| howard-ann |
0.12.1.0 |
HOWARD - Highly Open Workflow for Annotation & Ranking toward genomic variant Discovery |
2024-12-20 12:16:57 |
| genomicsdb |
0.0.9.18 |
Experimental Python Bindings for querying GenomicsDB |
2024-12-19 20:41:33 |
| variant |
0.0.94 |
None |
2024-11-10 19:23:19 |
| igv-reports |
1.14.1 |
Creates self-contained html pages for visual variant review with IGV (igv.js). |
2024-09-18 18:40:25 |
| varpepdb |
1.0.3 |
Generate reference database of variant peptides for peptide spectrum matching |
2024-09-07 05:11:18 |
| palamedes |
0.0.8 |
Palamedes: HGVS variants from a sequence alignment |
2024-06-13 17:50:03 |