Evidence map›Paper›PMID 30346945›Full record

ArticlePLoS biology2018

Quantitative assessment of cell population diversity in single-cell landscapes.

Qi Liu, Charles A Herring, Quanhu Sheng, Jie Ping, Alan J Simmons, Bob Chen, Amrita Banerjee, Wei Li, Guoqiang Gu, Robert J Coffey and 2 more

Abstract read
In one paragraph

Article in PLoS biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

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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

12 authors.

Qi LiuDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Charles A HerringEpithelial Biology Center, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Quanhu ShengDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Jie PingDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Alan J SimmonsEpithelial Biology Center, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Bob ChenEpithelial Biology Center, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Amrita BanerjeeEpithelial Biology Center, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Wei LiEpithelial Biology Center, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Guoqiang GuDepartment of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America.
Robert J CoffeyEpithelial Biology Center, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Yu ShyrDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Ken S LauCenter for Quantitative Sciences, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.ORCID 0000-0001-8438-0319

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI STACIE B DUSETZINA · 1995 to 2026
$172.8M
TISSUE CoreP50CA098131 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PARK, BEN HO, PIETENPOL, JENNIFER A · 2003 to 2024
$48.7M
Understanding and Controlling p120 Dysfunction in CRCP50CA095103 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI COFFEY, ROBERT J. · 2002 to 2017
$33.6M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
Vanderbilt-Ingram Cancer Center SPORE in Gastrointestinal CancerP50CA236733 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Robert J. Coffey · 2019 to 2026
$19.6M
Molecular, Cellular and Tissue Characterization UnitU2CCA233291 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI COFFEY, ROBERT J. · 2018 to 2023
$12.2M
Integrated approach to study early and late events in colonic neoplasia: mouse to manR35CA197570 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Robert J. Coffey · 2017 to 2026
$9.4M
Training Program in Stem Cell and Regenerative Developmental BiologyT32HD007502 · NICHD · VANDERBILT UNIVERSITY · PI WRIGHT, CHRISTOPHER V · 1997 to 2022
$5.4M
The Mechanisms of Islet Cell Specification and DifferentiationR01DK065949 · NIDDK · VANDERBILT UNIVERSITY · PI GU, GUOQIANG · 2004 to 2017
$4.4M
Tuft cell heterogeneity in function, lineage, and structure in ileal inflammatory diseaseR01DK103831 · NIDDK · VANDERBILT UNIVERSITY · PI LAU, KEN S · 2016 to 2024
$4.4M
Systems approaches to understanding the relationships between genotype, signaling, and therapeutic efficacyU01CA215798 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI HAAS, WILHELM, HAIGIS, KEVIN · 2017 to 2021
$3.7M
The DNA methylome-based regulation of functional beta-cell massR01DK125696 · NIDDK · VANDERBILT UNIVERSITY · PI Guoqiang Gu · 2020 to 2026
$3.4M
NCI NIH HHS P30 CA068485NCI NIH HHS P50 CA095103NCI NIH HHS P50 CA098131NCI NIH HHS P50 CA236733NCI NIH HHS R35 CA197570NCI NIH HHS U01 CA215798NCI NIH HHS U24 CA163056NCI NIH HHS U2C CA233291NICHD NIH HHS T32 HD007502NIDDK NIH HHS P30 DK058404NIDDK NIH HHS R01 DK065949NIDDK NIH HHS R01 DK103831NIDDK NIH HHS R01 DK125696NIGMS NIH HHS F31 GM120940NLM NIH HHS T32 LM012412
6 · The paper itself

Abstract

Single-cell RNA sequencing (scRNA-seq) has become a powerful tool for the systematic investigation of cellular diversity. As a number of computational tools have been developed to identify and visualize cell populations within a single scRNA-seq dataset, there is a need for methods to quantitatively and statistically define proportional shifts in cell population structures across datasets, such as expansion or shrinkage or emergence or disappearance of cell populations. Here we present sc-UniFrac, a framework to statistically quantify compositional diversity in cell populations between single-cell transcriptome landscapes. sc-UniFrac enables sensitive and robust quantification in simulated and experimental datasets in terms of both population identity and quantity. We have demonstrated the utility of sc-UniFrac in multiple applications, including assessment of biological and technical replicates, classification of tissue phenotypes and regional specification, identification and definition of altered cell infiltrates in tumorigenesis, and benchmarking batch-correction tools. sc-UniFrac provides a framework for quantifying diversity or alterations in cell populations across conditions and has broad utility for gaining insight into tissue-level perturbations at the single-cell resolution.

Indexed as

AnimalsBrainCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCluster AnalysisComputer SimulationDatabases, Nucleic AcidGene Expression ProfilingHumansIntestinal MucosaMiceMice, Inbred C57BLModels, BiologicalNeoplasms, ExperimentalOligodendrogliaSequence Analysis, RNA

Identifiers

PMID30346945
PMCPMC6211764

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.