Evidence map›Paper›PMID 29713661›Full record

ReviewCellular and molecular gastroenterology and hepatology2018

Single-Cell Computational Strategies for Lineage Reconstruction in Tissue Systems.

Charles A Herring, Bob Chen, Eliot T McKinley, Ken S Lau

Abstract readReview
In one paragraph

Review in Cellular and molecular gastroenterology and hepatology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 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

4 authors.

Charles A HerringEpithelial Biology Center, Vanderbilt University Medical Center, Nashville, Tennessee.
Bob ChenEpithelial Biology Center, Vanderbilt University Medical Center, Nashville, Tennessee.
Eliot T McKinleyEpithelial Biology Center, Vanderbilt University Medical Center, Nashville, Tennessee.
Ken S LauEpithelial Biology Center, Vanderbilt University Medical Center, Nashville, Tennessee.

Funding

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
Multidisciplinary Training in Basic and Translational Imaging of CancerR25CA092043 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MANNING, HENRY CHARLES · 2001 to 2015
$6.6M
Training Program in Stem Cell and Regenerative Developmental BiologyT32HD007502 · NICHD · VANDERBILT UNIVERSITY · PI WRIGHT, CHRISTOPHER V · 1997 to 2022
$5.4M
Tuft cell heterogeneity in function, lineage, and structure in ileal inflammatory diseaseR01DK103831 · NIDDK · VANDERBILT UNIVERSITY · PI LAU, KEN S · 2016 to 2024
$4.4M
BIDS: Vanderbilt Training Program in BIg Biomedical Data ScienceT32LM012412 · NLM · VANDERBILT UNIVERSITY · PI BLUME, JEFFREY D., GADD, CYNTHIA S · 2016 to 2020
$1.5M
Leveraging SingleCell Data to Define Cell Differentiation TransitionsF31GM120940 · NIGMS · VANDERBILT UNIVERSITY · PI HERRING, CHARLES A. · 2016 to 2017
$54k
NCI NIH HHS P50 CA095103NCI NIH HHS R25 CA092043NICHD NIH HHS T32 HD007502NIDDK NIH HHS P30 DK058404NIDDK NIH HHS R01 DK103831NIGMS NIH HHS F31 GM120940NLM NIH HHS T32 LM012412
6 · The paper itself

Abstract

Function at the organ level manifests itself from a heterogeneous collection of cell types. Cellular heterogeneity emerges from developmental processes by which multipotent progenitor cells make fate decisions and transition to specific cell types through intermediate cell states. Although genetic experimental strategies such as lineage tracing have provided insights into cell lineages, recent developments in single-cell technologies have greatly increased our ability to interrogate distinct cell types, as well as transitional cell states in tissue systems. From single-cell data that describe these intermediate cell states, computational tools have been developed to reconstruct cell-state transition trajectories that model cell developmental processes. These algorithms, although powerful, are still in their infancy, and attention must be paid to their strengths and weaknesses when they are used. Here, we review some of these tools, also referred to as

Indexed as

Cell State TransitionDifferentiationMST, minimum spanning treePCA, principal component analysisPseudotimescRNA-seq, single-cell RNA-sequencingSingle-Cell AnalysisStem CellsTrajectoryt-SNE, t-distributed stochastic neighbor embedding

Identifiers

PMID29713661
PMCPMC5924749

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.