numbat
1.5.2Haplotype-Aware CNV Analysis from scRNA-Seq
Overview
A computational method that infers copy number variations (CNVs) in cancer scRNA-seq data and reconstructs the tumor phylogeny. 'numbat' integrates signals from gene expression, allelic ratio, and population haplotype structures to accurately infer allele-specific CNVs in single cells and reconstruct their lineage relationship. 'numbat' can be used to: 1. detect allele-specific copy number variations from single-cells; 2. differentiate tumor versus normal cells in the tumor microenvironment; 3. infer the clonal architecture and evolutionary history of profiled tumors. 'numbat' does not require tumor/normal-paired DNA or genotype data, but operates solely on the donor scRNA-data data (for example, 10x Cell Ranger output). Additional examples and documentations are available at https://kharchenkolab.github.io/numbat/. For details on the method please see Gao et al. Nature Biotechnology (2022) doi:10.1038/s41587-022-01468-y.
Install
Health
- NOTE r-devel-linux-x86_64-fedora-clang
- NOTE r-devel-linux-x86_64-fedora-gcc
- NOTE2026-06-0911 OK · 2 NOTE · 0 WARNING · 0 ERROR · 0 FAILURE
- ERROR2026-06-0810 OK · 2 NOTE · 0 WARNING · 1 ERROR · 0 FAILURE
- NOTE2026-05-1011 OK · 2 NOTE · 0 WARNING · 0 ERROR · 0 FAILURE
- ERROR2026-05-0310 OK · 2 NOTE · 0 WARNING · 1 ERROR · 0 FAILURE
- NOTE2026-04-229 OK · 5 NOTE · 0 WARNING · 0 ERROR · 0 FAILURE
Show 2 earlier snapshots
- ERROR2026-04-188 OK · 5 NOTE · 0 WARNING · 1 ERROR · 0 FAILURE
- NOTE2026-03-109 OK · 5 NOTE · 0 WARNING · 0 ERROR · 0 FAILURE
Documentation
- Examples that run
- 100%
- Documented parameters
- 100%
- Return-value docs
- 100%
- References docs
- 0%
Downloads
Repository
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Repository practices
4 development-tooling and community-health practices detected across 3 families in the upstream repository
Checks run against github.com/kharchenkolab/numbat on 2026-07-19.
Dependencies
Nothing depends on this yet.
Code & Tests
- Cyclomatic complexity
- 2.0 median / 33 max
- Test cases
- 1 / 0.00 per code line
- System requirements
- 1 external
Test coverage
Line coverage
–
Expression
–
Tests / Examples
–
Functions
142 15 exported
Complexity
3 avg / 33 max
Call network
142 nodes / 169 edges
Call graph
Open call graph →Lowest coverage
Per-function coverage is not measured for this package yet.
Datasets
| Name | Class | Rows × Cols | Also ships in |
|---|---|---|---|
| acen_hg19 | tbl_df/tbl/data.frame | 22 × 3 | in 2 packages |
| acen_hg38 | tbl_df/tbl/data.frame | 22 × 3 | in 2 packages |
| annot_ref | data.frame | 50 × 2 | – |
| bulk_example | tbl_df/tbl/data.frame | 3,935 × 83 | – |
| df_allele_example | data.frame | 41,167 × 11 | – |
| gexp_roll_example | data.frame | 10 × 2,000 | – |
| vcf_meta | vector | – | in 2 packages |
People & History
11 releases. Pick two to compare their code metrics. R releases are shown for context.
- RR 4.6.0 released · 2026-04-24
- 1.5.2Latest
- unarchivedReturned to CRAN2026-02-04
- archivedRemoved from CRAN2026-01-30requires archived package 'pryr'
- 1.5.12025-10-21 · diff ↗
- RR 4.5.0 released · 2025-04-11
- 1.4.22024-09-20 · diff ↗
- RR 4.4.0 released · 2024-04-24
- 1.4.02024-02-23 · diff ↗
- 1.3.2-12023-06-17 · diff ↗
- 1.3.22023-06-06 · diff ↗
- RR 4.3.0 released · 2023-04-21
- 1.3.02023-04-02 · diff ↗
- 1.2.22023-02-14 · diff ↗
- 1.2.12023-01-11 · diff ↗
- 1.1.02022-11-29 · diff ↗
Show 2 earlier events
- 1.0.22022-09-15
- RR 4.2.0 released · 2022-04-22
Package metadata
- First published
- 2022-09-15
- Total releases
- 11 / 4 yrs
- License
- MIT + file LICENSE OSI
- Minimum R
- ≥ 4.1.0
- Bundled data
- 3.8 MB / 24 files
- Download size
- 4.1 MB
- Installed size
- not tracked yet
- With dependencies
- not tracked yet