cellOrigins
0.1.3Finds RNASeq Source Tissues Using In Situ Hybridisation Data
Overview
Finds the most likely originating tissue(s) and developmental stage(s) of tissue-specific RNA sequencing data. The package identifies both pure transcriptomes and mixtures of transcriptomes. The most likely identity is found through comparisons of the sequencing data with high-throughput in situ hybridisation patterns. Typical uses are the identification of cancer cell origins, validation of cell culture strain identities, validation of single-cell transcriptomes, and validation of identity and purity of flow-sorting and dissection sequencing products.
Install
Health
- NOTE r-devel-linux-x86_64-debian-clang
- NOTE r-devel-linux-x86_64-debian-gcc
- NOTE2026-03-1012 OK · 2 NOTE · 0 WARNING · 0 ERROR · 0 FAILURE
Downloads
Dependencies
Nothing depends on this yet.
Code & Tests
- Cyclomatic complexity
- 1.0 median / 3 max
Test coverage
Line coverage
–
Expression
–
Tests / Examples
–
Functions
12 0 exported
Complexity
1.7 avg / 3 max
Call network
12 nodes / 3 edges
Test coverage has not been measured for this package yet; nodes fall back to a neutral fill.
Call graph
Open call graph →Lowest coverage
Per-function coverage is not measured for this package yet.
People & History
Author records are not tracked yet for this package.
1 release. R releases are shown for context.
- RR 4.6.0 released · 2026-04-24
- 0.1.3Latest2026-03-10 · current release
- RR 4.5.0 released · 2025-04-11
Package metadata
- First published
- 2020-06-05
- Total releases
- 1 / 6 yrs
- License
- CC BY-NC-SA 4.0
- Bundled data
- 52 KB / 1 file
- Download size
- 323 KB
- Installed size
- not tracked yet
- With dependencies
- not tracked yet