Name | Version | Summary | date |
cytetype |
0.9.1 |
Python client for characterization of clusters from single-cell RNA-seq data. |
2025-08-25 00:48:30 |
varseek |
0.1.1 |
Efficient variant screening of RNA-seq and DNA-seq data using k-mer-based alignment against a reference of known variants. |
2025-08-12 08:17:59 |
omicverse |
1.7.7 |
OmicVerse: A single pipeline for exploring the entire transcriptome universe |
2025-08-11 13:52:04 |
heartmap |
1.1.1 |
Heart Multi-chamber Analysis Platform for single-cell RNA-seq |
2025-08-06 19:39:24 |
basepair |
2.2.5 |
Python client for Basepair's API |
2025-02-05 11:50:32 |
gene-scoring |
0.1.4 |
Gene set scoring package for single-cell RNA sequencing data with GPU acceleration. |
2025-02-03 07:05:57 |
fastQpick |
0.1.0 |
Fast and memory-efficient sampling of DNA-Seq or RNA-seq fastq data with or without replacement. |
2025-01-22 23:02:48 |
WonderPeaks |
0.1.10 |
functions for peakcalling enriched peaks in ChIP-seq and untranslateed regions in 3'RNA-seq in Fungi |
2025-01-17 19:15:59 |
WonderPeaks-preprocessing |
0.2.3 |
preprocessing functions for ChIP-seq and RNA-seq in Fungi with WonderPeaks |
2025-01-17 01:49:05 |
Augusta |
1.0.6 |
Python package for inference of the gene regulatory network and the boolean network using RNA-Seq data. |
2024-12-02 13:08:10 |
salusts |
2.8.6 |
A Python package for SaluSTS workflow. |
2024-11-06 06:52:20 |
dogma-data |
0.2.19 |
Data processing for Dogma |
2024-11-04 21:48:10 |
DeSide |
1.3.2 |
A unified DEep-learning and SIngle-cell based DEconvolution method for solid tumors |
2024-09-15 16:18:47 |
omicfate |
0.0.1 |
OmicFate: Unraveling the Secrets of Cellular Fate Determination |
2024-07-19 08:33:46 |
ncbi-counts |
0.2.0 |
Download the NCBI-generated RNA-seq count data by specifying the Series accession number(s), and the regular expression of the Sample attributes. |
2024-06-04 10:34:45 |