Evidence map›Paper›PMID 32352970›Full record

ArticlePloS one2020

Sequence count data are poorly fit by the negative binomial distribution.

Stijn Hawinkel, J C W Rayner, Luc Bijnens, Olivier Thas

Abstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  8. Detecting differential transcript usage in complex diseases with SPIT.bioRxiv : the preprint server for biology · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Stijn HawinkelDepartment of Data Analysis and Mathematical Modelling, Ghent University, Ghent, Belgium.ORCID 0000-0002-4501-5180
J C W RaynerCentre for Computer-Assisted Research in Mathematics and its Applications, School of Mathematical and Physical Sciences, University of Newcastle, Newcastle, Australia.ORCID 0000-0003-4987-0026
Luc BijnensQuantitative Sciences, Janssen Pharmaceutical companies of Johnson and Johnson, Ghent, Belgium.ORCID 0000-0002-4126-3152
Olivier ThasDepartment of Data Analysis and Mathematical Modelling, Ghent University, Ghent, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sequence count data are commonly modelled using the negative binomial (NB) distribution. Several empirical studies, however, have demonstrated that methods based on the NB-assumption do not always succeed in controlling the false discovery rate (FDR) at its nominal level. In this paper, we propose a dedicated statistical goodness of fit test for the NB distribution in regression models and demonstrate that the NB-assumption is violated in many publicly available RNA-Seq and 16S rRNA microbiome datasets. The zero-inflated NB distribution was not found to give a substantially better fit. We also show that the NB-based tests perform worse on the features for which the NB-assumption was violated than on the features for which no significant deviation was detected. This gives an explanation for the poor behaviour of NB-based tests in many published evaluation studies. We conclude that nonparametric tests should be preferred over parametric methods.

Indexed as

Binomial DistributionMicrobiotaPoisson DistributionRegression AnalysisRNA, Ribosomal, 16SRNA-SeqRNA, Ribosomal, 16S

Identifiers

PMID32352970
PMCPMC7192467

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.