Name | Version | Summary | date |
snpio |
1.6.0 |
SNPio is a Python API for population genetic file processing, filtering, and analysis. It is designed to be a user-friendly tool for the manipulation of population genetic data in a variety of formats. SNPio can be used to filter data based on missingness, MAF and MAC, singletons, biallelic, and monomorphic sites. It can also generate summary statistics for population genetic analyses. |
2025-07-25 08:41:06 |
stranger |
0.9.4 |
Annotate VCF files with STR variants with pathogenicity implications |
2025-03-04 12:43:47 |
aspose-total-net |
25.1.0 |
Aspose.Total for Python via .NET is a Document Processing python class library that allows developers to work with Microsoft Word®, Microsoft PowerPoint®, Microsoft Outlook®, OpenOffice®, & 3D file formats without needing Office Automation. |
2025-02-03 18:11:00 |
scout-browser |
4.94.1 |
Clinical DNA variant visualizer and browser |
2024-12-20 16:20:01 |
genomicsdb |
0.0.9.18 |
Experimental Python Bindings for querying GenomicsDB |
2024-12-19 20:41:33 |
card-data-parsers |
0.17.0 |
Parsing bank feed data files |
2024-11-26 13:36:05 |
biophony |
1.2.1 |
Random generation of genetic files |
2024-11-18 15:25:26 |
genmod |
3.9 |
Annotate genetic inheritance models in variant files |
2024-10-24 08:31:12 |
vcf2maf-lite |
0.1.1 |
VCF to MAF format converter |
2024-07-30 21:38:59 |
dcicpyvcf |
3.1.0 |
Variant Call Format (VCF) parser for Python |
2024-07-03 09:43:58 |
vmware-vcenter |
4.3.0 |
Client library for vSphere Automation APIs |
2024-07-01 09:37:10 |
vmware-vapi-runtime |
2.52.0 |
VMware vAPI Runtime |
2024-06-13 07:27:45 |
vmware-vapi-common-client |
2.52.0 |
VMware vAPI Common Services Client Bindings |
2024-06-13 07:25:29 |