Evidence map›Paper›PMID 41770747›Full record

ArticlePLoS computational biology2026

Assessment of dispersion metrics for estimating single-cell transcriptional variability.

Tina Chen, Laurie A Boyer, Divyansh Agarwal

Abstract read
In one paragraph

Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. Article
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

3 authors.

Tina ChenMassachusetts Institute of Technology, Department of Electrical Engineering and Computer Science, Cambridge, Massachusetts, United States of America.ORCID https://orcid.org/0009-0007-9542-7777
Laurie A BoyerMassachusetts Institute of Technology, Department of Biology, Cambridge, Massachusetts, United States of America.ORCID https://orcid.org/0000-0003-3491-4962
Divyansh AgarwalMassachusetts Institute of Technology, Department of Biology, Cambridge, Massachusetts, United States of America.ORCID https://orcid.org/0000-0003-0404-6877

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-cell RNA sequencing data enables analysis of transcript levels of single cells across different cell types and conditions. Recent work has highlighted the value of measuring gene-specific transcriptional variability, or noise, within a genetically identical population of cells in addition to mean expression, given that these differences contribute to biological processes including development and disease. However, measuring transcriptional noise remains a challenge. Here, we systematically compared statistical methods by simulating single-cell data by varying both dispersion and count size to assess the relative responsiveness to noise of several commonly used statistical metrics: the Gini index, variance-to-mean ratio, variance, coefficient of variance (CV), CV2, and Shannon entropy. We found that the variance-to-mean ratio scales approximately linearly with increasing dispersion and is independent of dataset size. In contrast, the Gini index displayed paradoxical behavior in that it increases as dispersion decreases, and Shannon entropy was not scale-invariant. Next, we applied the variance-to-mean ratio (Fano factor) to measure transcriptional variability in single-cell datasets representing different complex systems and cross-platform measurements. Our data show that many genes display transcriptional variability within the same cell type, and that while variation does not correlate with gene characteristics such as transcript level, promoter GC content, or evolutionary gene age, variable genes are often correlated with specific biological processes. Notably, most genes and pathways with highest transcriptional variability as identified by the Fano factor were largely independent of differentially expressed genes and have also been implicated in biological processes related to the system. Thus, our data highlight that choice and application of appropriate models for measuring transcriptional variation in scRNA-seq data can reveal biologically relevant information beyond what is observed from mean expression alone.

Indexed as

Sequence Analysis, RNASingle-Cell AnalysisTranscription, GeneticAnimalsComputational BiologyComputer SimulationGene Expression ProfilingHumansSingle-Cell Gene Expression Analysis

Identifiers

PMID41770747
PMCPMC12970974

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.