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fluentGenomics

Bioc current

A plyranges and tximeta workflow

v1.24.0 · Package record · workflows · MIT + file LICENSE

Release Lineage

Entered 3.11 · Apr 28, 2020

Current · Requires R 4.6

1.0 In 13 of 49 releases 3.23

Description

An extended workflow using the plyranges and tximeta packages for fluent genomic data analysis. Use tximeta to correctly import RNA-seq transcript quantifications and summarize them to gene counts for downstream analysis. Use plyranges for clearly expressing operations over genomic coordinates and to combine results from differential expression and differential accessibility analyses.

Advisories

None published for Bioconductor

Test coverage

Line coverage

–

Expression

–

Tests / Examples

–

Functions

5 1 exported

Complexity

1.8 avg / 3 max

Call network

5 nodes / 4 edges

Test coverage is not measured for Bioconductor packages; nodes fall back to a neutral fill.

Loading call graph…

Lowest coverage

Per-function coverage is not measured for this package yet.

Code

Structure

Lines of code

1,298

Files

13

Compiled share

0%

Has compiled src

No

Language breakdown

R 133 (10.2%)Docs 55 (4.2%)Vignettes 1,110 (85.5%)

API

Exported functions

1

Internal functions

4

Testing

Has tests

No

Test-to-code ratio

0.00

testthat edition

–

Docs

Roxygen coverage

100%

Health & Security signals

Informational signals; not verdicts.

on.exit coverage

100%

Unsafe pattern score

0

Dep constraint coverage

16.7%

Secret pattern count

0

Bundled 3rd-party code

2 items

Portability & License

Min R version

4.0

System requirements

–

C++ standard

–

License

MIT + file LICENSE

License flags

SPDX valid, OSI approved

History

Versions

13

First release

2020-05-22

Latest release

2026-04-28

Avg cadence

182 days

Cold removal rate

–

Dep drift

0

LOC over versions

v3.11: 1,297 LOCv3.12: 1,297 LOCv3.13: 1,297 LOCv3.14: 1,297 LOCv3.15: 1,297 LOCv3.16: 1,297 LOCv3.17: 1,297 LOCv3.18: 1,297 LOCv3.19: 1,297 LOCv3.20: 1,297 LOCv3.21: 1,297 LOCv3.22: 1,298 LOCv3.23: 1,298 LOC

Per-file churn detail lives in the source pipeline: https://github.com/r-observatory/bioc-code-metrics.

Documentation

In the Bioconductor 3.23 release
READMEYes · 135 wordsVignettesYes · 1 · dynamicNEWSYes · 100% structuredCitation fileNo
Help pages
2
Examples that run
100%1 run in a plain check (under a condition)
Exported functions with examples
100%
Documented parameters
100%
Return-value docs
100%
Help pages citing references
0%
Vignettes (1)

Repository practices

Upstream repositoryBeta

7 development-tooling and community-health practices detected across 4 families in the upstream repository

Checks run against github.com/sa-lee/fluentgenomics on 2026-10-21.

Continuous integration (2)
GitHub ActionsR CMD check workflow

The R CMD check workflow runs on Linux and macOS, and on R-devel

Docs source (3)
pkgdown

GitHub Pages site last deployed 2026-06-10 · The repository has a site deploy workflow

Coverage (1)
Coverage reporting
Reproducibility and dev environment (1)
Makefile
How this is detected·Detection ruleset v4 (2026-10-20)

Datasets

Bundled datasets · 1
NameClassSizeAlso in
peaks–––

All of fluentGenomics's data objects

Topics

Maintainer
Stuart Lee

Available on

CRANr2uBioconductorautoCRANCOPR

People

Cite

Cite this package

Run in R for the authors' preferred citation:

citation("fluentGenomics")
Lee, S., & Love, M. (2026). fluentGenomics: A plyranges and tximeta workflow (Version 1.24.0) [Computer software]. https://bioconductor.org/packages/fluentGenomics

This package has no citation file, so citation() returns this entry built from DESCRIPTION.

Cite the R Observatory

For a number measured here: a download total, a coverage figure, an archival date.

APA

Balamuta, J. J. (2026). R Observatory: Metrics for fluentGenomics version 1.24.0 [Data set]. HJJB, LLC. Data release v2026-10-23. https://doi.org/10.5281/zenodo.21843040

From data release v2026-10-23, which the citation names so these numbers can be found later. More on citing and the projects behind them.

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