sangerseqR
Bioc currentTools for Sanger Sequencing Data in R
Release Lineage
Entered 2.14 · Apr 14, 2014
Current · Requires R 4.6
Description
This package contains several tools for analyzing Sanger Sequencing data files in R, including reading .scf and .ab1 files, making basecalls and plotting chromatograms.
Test coverage
Line coverage
–
Expression
–
Tests / Examples
–
Functions
18 4 exported
Complexity
2.5 avg / 19 max
Call network
18 nodes / 16 edges
Test coverage is not measured for Bioconductor packages; nodes fall back to a neutral fill.
Call graph
Open call graph →Lowest coverage
Per-function coverage is not measured for this package yet.
Code
Structure
Lines of code
2,729
Files
48
Compiled share
0%
Has compiled src
No
Language breakdown
API
Exported functions
22
Internal functions
14
Testing & CI
Has tests
Yes
Test-to-code ratio
0.00
testthat edition
–
CI present
No
CI type
[]
PR gated
No
Docs
Roxygen coverage
100%
Health & Security signals
Informational signals; not verdicts.
on.exit coverage
0%
Unsafe pattern score
0
Dep constraint coverage
0%
Secret pattern count
0
Bundled 3rd-party code
2 items
Portability & License
Min R version
3.5.0
System requirements
–
C++ standard
–
License
GPL-2
License flags
SPDX valid, OSI approved
History
Versions
25
First release
2014-04-11
Latest release
2026-04-28
Avg cadence
183 days
Cold removal rate
–
Dep drift
3
LOC over versions
Per-file churn detail lives in the source pipeline: https://github.com/r-observatory/bioc-code-metrics.
Documentation
- Examples that run
- 91%
- Documented parameters
- 100%
- Return-value docs
- 78%
- References docs
- 17%
Topics
Depended on by (3)
Bioconductor (3)
People
Jonathon Hill
Cite
Cite this package
Run in R for the authors' preferred citation:
citation("sangerseqR")Cite the R Observatory
For a number measured here: a download total, a coverage figure, an archival date.
From data release v2026-08-24, which the citation names so these numbers can be found later. More on citing and the projects behind them.