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ppcseq

Bioc current

Probabilistic Outlier Identification for RNA Sequencing Generalized Linear Models

v1.20.0 · software · GPL-3

Release Lineage

Entered 3.13 · May 20, 2021

Current · Requires R 4.6

1.0 In 11 of 49 releases 3.23

Description

Relative transcript abundance has proven to be a valuable tool for understanding the function of genes in biological systems. For the differential analysis of transcript abundance using RNA sequencing data, the negative binomial model is by far the most frequently adopted. However, common methods that are based on a negative binomial model are not robust to extreme outliers, which we found to be abundant in public datasets. So far, no rigorous and probabilistic methods for detection of outliers have been developed for RNA sequencing data, leaving the identification mostly to visual inspection. Recent advances in Bayesian computation allow large-scale comparison of observed data against its theoretical distribution given in a statistical model. Here we propose ppcseq, a key quality-control tool for identifying transcripts that include outlier data points in differential expression analysis, which do not follow a negative binomial distribution. Applying ppcseq to analyse several publicly available datasets using popular tools, we show that from 3 to 10 percent of differentially abundant transcripts across algorithms and datasets had statistics inflated by the presence of outliers.

Test coverage

Line coverage

Expression

Tests / Examples

Functions

40 2 exported

Complexity

1.7 avg / 12 max

Call network

40 nodes / 58 edges

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

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Lowest coverage

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

Code

Structure

Lines of code

2,750

Files

43

Compiled share

0.9%

Has compiled src

Yes

Language breakdown

R 2,357 (85.7%)C/C++/src 25 (0.9%)Tests 65 (2.4%)Docs 187 (6.8%)Vignettes 116 (4.2%)

API

Exported functions

2

Internal functions

37

Testing & CI

Has tests

Yes

Test-to-code ratio

0.03

testthat edition

3

CI present

Yes

CI type

["github-actions","travis"]

PR gated

Yes

Docs

Roxygen coverage

100%

Health & Security signals

Informational signals; not verdicts.

on.exit coverage

Unsafe pattern score

2

Dep constraint coverage

23.8%

Secret pattern count

0

Bundled 3rd-party code

2 items

Portability & License

Min R version

4.1.0

System requirements

1

C++ standard

C++14

License

GPL-3

License flags

SPDX valid, OSI approved

History

Versions

11

First release

2021-05-19

Latest release

2026-04-28

Avg cadence

182 days

Cold removal rate

Dep drift

3

LOC over versions

v3.13: 2,902 LOCv3.14: 2,902 LOCv3.15: 2,902 LOCv3.16: 2,902 LOCv3.17: 2,903 LOCv3.18: 2,750 LOCv3.19: 2,750 LOCv3.20: 2,750 LOCv3.21: 2,750 LOCv3.22: 2,750 LOCv3.23: 2,750 LOC

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

Documentation

Documentation
READMEYes · 399 wordsVignettesYes · dynamicpkgdown siteNoNEWSNoCode of conductNoContributing guideNo
Examples that run
100%
Documented parameters
92%
Return-value docs
100%
References docs
25%

Topics

People

Cite

Cite this package

Run in R for the authors' preferred citation:

citation("ppcseq")
Mangiola, S. (2026). ppcseq: Probabilistic Outlier Identification for RNA Sequencing Generalized Linear Models (Version 1.20.0) [Computer software]. https://bioconductor.org/packages/ppcseq

This is what citation() produces when a package has no citation file of its own. If it prints something else, use that.

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 ppcseq version 1.20.0 [Data set]. HJJB, LLC. Data release v2026-08-08. https://doi.org/10.5281/zenodo.21843040

From data release v2026-08-08, which the citation names so these numbers can be found later. More on citing and the projects behind them.

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