Project Name | Stars | Downloads | Repos Using This | Packages Using This | Most Recent Commit | Total Releases | Latest Release | Open Issues | License | Language |
---|---|---|---|---|---|---|---|---|---|---|
Codex2 | 29 | 3 years ago | 1 | gpl-2.0 | R | |||||
Full-spectrum copy number variation detection by high-throughput DNA sequencing | ||||||||||
Shallowhrd | 28 | 6 months ago | R | |||||||
This method uses shallow Whole Genome Sequencing (sWGS) and the segmentation of a genomic profile to assess the Homologous Recombination Deficiency of a tumor based on the number of Large-scale Genomic Alterations (LGAs). | ||||||||||
Eacon | 14 | 3 years ago | 3 | mit | R | |||||
Easy Copy Number ! | ||||||||||
Hammlet | 10 | 4 years ago | 2 | gpl-3.0 | C++ | |||||
Fast Bayesian Hidden Markov Model with Wavelet Compression | ||||||||||
Cometgazer | 8 | 5 years ago | Shell | |||||||
COMETgazer mehylation analysis software suite | ||||||||||
Codex | 8 | 5 years ago | gpl-2.0 | R | ||||||
A normalization and copy number variation calling procedure for whole exome DNA sequencing data. | ||||||||||
Ideas_2018 | 5 | 4 years ago | 4 | mit | C++ | |||||
Jointly characterizing epigenetic dynamics across multiple cell types |