infercnvpy
importedsoftware/infercnvpy
Infer copy number variation (CNV) from scRNA-seq data. Plays nicely with Scanpy.
Machine-generated from the listed sources and not yet reviewed by a human.
- Category
- Software & Systems
- Subcategory
- unknown
- License
- BSD-3-Clause(osi)
- Status
- active
- Maturity
- deployed
- Organization
- icbi-lab
- Country
- unknown
- Repository
- github.com/icbi-lab/infercnvpy
- Documentation
- unknown
- Tags
- cnv · scverse · single-cell
- Regulatory
- unknown
Top contributors by commit count, from the project’s public repository. Avatars are served by their origin, not stored here. To be removed from this list, open an issue.
Computed from shared tags, weighted so a rare tag counts for more than a common one. These are suggestions, not curated relationships.
- decouplerscverse · single-cell
Python package to perform enrichment analysis from omics data.
- rapids-singlecellscverse · single-cell
rapids-singlecell: GPU-accelerated framework for scRNA analysis
- alphapepttoolsscverse
Search- and quantification-engine agnostic biological interpretation of proteomics data
- anndatascverse
Annotated data.
- ehrapyscverse
Electronic Health Record Analysis with Python.
- mudatascverse
Multimodal Data (.h5mu) implementation for Python
- api.github.com/repos/icbi-lab/infercnvpyretrieved 2026-08-05 · via github-api
Machine-imported from GitHub search. Last push 2026-08-03, 196 stars, license reported as BSD-3-Clause. Category and schematic were assigned by keyword heuristics and are unreviewed.
Not yet verified by a human. Correct this record →
/v1/entries/3.json→ .entries["infercnvpy"]
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