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https://github.com/broadinstitute/inferCNV
Inferring CNV from Single-Cell RNA-Seq
https://github.com/broadinstitute/inferCNV
Last synced: 24 days ago
JSON representation
Inferring CNV from Single-Cell RNA-Seq
- Host: GitHub
- URL: https://github.com/broadinstitute/inferCNV
- Owner: broadinstitute
- License: other
- Created: 2016-03-14T21:53:54.000Z (over 8 years ago)
- Default Branch: master
- Last Pushed: 2023-12-01T18:34:58.000Z (7 months ago)
- Last Synced: 2024-02-14T14:45:02.471Z (5 months ago)
- Language: R
- Homepage:
- Size: 22.6 MB
- Stars: 491
- Watchers: 41
- Forks: 156
- Open Issues: 176
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Metadata Files:
- Readme: README.md
- License: LICENSE
Lists
- awesome_single_cell - inferCNV - [R] - Part of the TrinityCTAT (Trinity Cancer Transcriptome Analysis Toolkit). Provides tools for copy-number inference from single-cell RNA-seq data. (Software packages / RNA-seq)
- awesome-single-cell - inferCNV - [R] - Part of the TrinityCTAT (Trinity Cancer Transcriptome Analysis Toolkit). Provides tools for copy-number inference from single-cell RNA-seq data. (Software packages / Copy number analysis)
- awesome-single-cell - inferCNV - [R] - Part of the TrinityCTAT (Trinity Cancer Transcriptome Analysis Toolkit). Provides tools for copy-number inference from single-cell RNA-seq data. (Software packages / RNA-seq)
README
Visit project [wiki](https://github.com/broadinstitute/inferCNV/wiki) for InferCNV documentation.