CNV
importedsoftware/cnv
Copy Number Variation
Machine-generated from the listed sources and not yet reviewed by a human.
- Category
- Software & Systems
- Subcategory
- unknown
- License
- MIT(osi)
- Status
- dormant
- Maturity
- deployed
- Organization
- unknown
- Country
- unknown
- Homepage
- unknown
- Repository
- github.com/flowhub-team/CNV
- Documentation
- unknown
- Tags
- cnv · copy-number-variation · copynumbervariation · genome · genomics
- 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.
- infercnvpycnv
Infer copy number variation (CNV) from scRNA-seq data. Plays nicely with Scanpy.
- SCEVANcopy-number-variation
R package that automatically classifies the cells in the scRNA data by segregating non-malignant cells of tumor microenviroment from the malignant cells. It also infers the copy number profile of…
- SCICoNEcopy-number-variation
Single-cell copy number calling and event history reconstruction.
- catchgenome · genomics
A package for designing compact and comprehensive capture probe sets.
- chromeistergenome · genomics
A dotplot generator for large chromosomes
- deepsomaticgenome · genomics
DeepSomatic is an analysis pipeline that uses a deep neural network to call somatic variants from tumor-normal and tumor-only sequencing data.
- api.github.com/repos/flowhub-team/CNVretrieved 2026-08-25 · via github-api
Machine-imported from GitHub search. Last push 2023-06-28, 53 stars, license reported as MIT. Category and schematic were assigned by keyword heuristics and are unreviewed.
Not yet verified by a human. Correct this record →
/v1/entries/38.json→ .entries["cnv"]
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