PyDigger - unearthing stuff about Python


NameVersionSummarydate
howard-ann 0.12.1.0 HOWARD - Highly Open Workflow for Annotation & Ranking toward genomic variant Discovery 2024-12-20 12:16:57
vcf2pandas 0.1.2 Package to convert a vcf into a pandas dataframe. 2024-12-06 00:57:56
tidy-vcf 0.2.1.0 Make tidy VCF data. 2024-09-06 19:41:08
snps 2.9.0 tools for reading, writing, merging, and remapping SNPs 2024-08-26 05:03:24
variant-extractor 4.0.8 Deterministic and standard extractor of indels, SNVs and structural variants (SVs) from VCF files 2024-07-17 08:31:05
vcf-generator 1.1.7 A simple VCF generator. Generate VCF files with random data. 2024-04-08 04:18:38
vatools 5.1.1 A tool for annotating VCF files with expression and readcount data 2024-02-05 15:34:46
vcfio 1.1.9 A simple and efficient VCF manipulation package. 2024-02-04 10:19:53
genomicspy 0.2.1 Tools for manipulating vcfs doing genomics work 2023-11-18 10:12:29
eva-vcf-merge 0.0.7 EBI EVA - VCF merge library 2023-10-05 23:07:00
wormtable 0.1.7 Write-once read-many data sets using Berkeley DB. 2023-10-05 13:28:04
HaploDynamics 0.4b1 A python library to develop genomic data simulators 2023-08-25 22:13:05
TelegramContract2vCard 1.0.0 make telegram contacts.html or result.json to vCard automatically 2023-08-07 12:01:21
hchacha 1.0.5 Human CHromosome Accession CHAnge - Convert between different human chromosome naming systems (of the same assembly/version) 2023-07-22 18:37:15
upd 0.2 Simple software to call UPD regions from germline exome/wgs trios. 2023-05-16 11:48:57
divbrowse 1.1.0 A web application for interactive visualization and analysis of genotypic variant matrices 2023-05-16 11:22:39
vcf-batcher 0.2.0 Command-line tool to cut VCF (variant call files) into smaller batches, intended to be used for multiprocessing or distributed computing. 2023-05-09 11:54:42
vcf_parser 1.6 Parsing vcf files 2016-11-01 12:05:38
vcftoolbox 1.5.1 Tools for manipulating and parsing vcf files 2016-05-11 11:28:08
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