Evidence map›Paper›PMID 39149226›Full record

ArticlebioRxiv : the preprint server for biology2024

Quantitative comparison of single-cell RNA sequencing versus single-molecule RNA imaging for quantifying transcriptional noise.

Neha Khetan, Binyamin Zuckerman, Giuliana P Calia, Xinyue Chen, Ximena Garcia Arceo, Leor S Weinberger

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Neha KhetanGladstone|UCSF Center for Cell Circuitry, University of California, San Francisco, CA 94158.ORCID 0000-0001-9972-1921
Binyamin ZuckermanGladstone|UCSF Center for Cell Circuitry, University of California, San Francisco, CA 94158.ORCID 0000-0002-6216-011X
Giuliana P CaliaGladstone|UCSF Center for Cell Circuitry, University of California, San Francisco, CA 94158.ORCID 0000-0001-7394-9565
Xinyue ChenGladstone|UCSF Center for Cell Circuitry, University of California, San Francisco, CA 94158.ORCID 0000-0001-8288-7685
Ximena Garcia ArceoGladstone|UCSF Center for Cell Circuitry, University of California, San Francisco, CA 94158.ORCID 0000-0001-9182-4870
Leor S WeinbergerGladstone|UCSF Center for Cell Circuitry, University of California, San Francisco, CA 94158.ORCID 0000-0002-9987-6357

Funding

UCSF IRACDA Scholars ProgramK12GM081266 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Raymond M. Esquerra, HOLLY A. INGRAHAM · 2007 to 2026
$19.4M
Modulating Stochastic Gene Expression for Cell-fate Control and TherapeuticsR37AI109593 · NIAID · J. DAVID GLADSTONE INSTITUTES · PI WEINBERGER, LEOR S · 2021 to 2025
$6.2M
Illumina NovaSeq 6000 Sequencing SystemS10OD028511 · OD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHOW, ERIC D · 2020 to 2020
$583k
Wide field-of-view Spinning Disk Confocal with Photoactivation and PhotobleachingS10OD017993 · OD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI THORN, KURT · 2015 to 2015
$274k
NIAID NIH HHS R37 AI109593NIGMS NIH HHS K12 GM081266NIH HHS S10 OD017993NIH HHS S10 OD028511
6 · The paper itself

Abstract

Stochastic fluctuations (noise) in transcription generate substantial cell-to-cell variability. However, how best to quantify genome-wide noise, remains unclear. Here we utilize a small-molecule perturbation (IdU) to amplify noise and assess noise quantification from numerous scRNA-seq algorithms on human and mouse datasets, and then compare to noise quantification from single-molecule RNA FISH (smFISH) for a panel of representative genes. We find that various scRNA-seq analyses report amplified noise, without altered mean-expression levels, for ~90% of genes and that smFISH analysis verifies noise amplification for the vast majority of genes tested. Collectively, the analyses suggest that most scRNA-seq algorithms are appropriate for quantifying noise including a simple normalization approach, although all of these systematically underestimate noise compared to smFISH. From a practical standpoint, this analysis argues that IdU is a globally penetrant noise-enhancer molecule-amplifying noise without altering mean-expression levels-which could enable investigations of the physiological impacts of transcriptional noise.

Indexed as

noise-enhancer moleculesingle-cell RNA sequencing (scRNA-seq)single molecule RNA FISH (smFISH)transcriptional noise

Identifiers

PMID39149226
PMCPMC11326230

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.