Evidence map›Paper›PMID 29269838›Full record

ArticleScientific reports2017

Micro-patterned agarose gel devices for single-cell high-throughput microscopy of E. coli cells.

David G Priest, Nobuyuki Tanaka, Yo Tanaka, Yuichi Taniguchi

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

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  12. Mammalian Cell Interaction with Periodic Surface Nanostructures.International journal of molecular sciences · 2022
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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.

David G PriestLaboratory for Single Cell Gene Dynamics, Quantitative Biology Center (QBiC), RIKEN, 6-2-3 Furuedai, Suita, Osaka, 565-0874, Japan.ORCID 0000-0003-0095-6718
Nobuyuki TanakaLaboratory for Integrated Biodevice, Quantitative Biology Center (QBiC), RIKEN, 1-3 Yamadaoka, Suita, Osaka, 565-0871, Japan.ORCID 0000-0002-4698-5867
Yo TanakaLaboratory for Integrated Biodevice, Quantitative Biology Center (QBiC), RIKEN, 1-3 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Yuichi TaniguchiLaboratory for Single Cell Gene Dynamics, Quantitative Biology Center (QBiC), RIKEN, 6-2-3 Furuedai, Suita, Osaka, 565-0874, Japan. taniguchi@riken.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-throughput microscopy of bacterial cells elucidated fundamental cellular processes including cellular heterogeneity and cell division homeostasis. Polydimethylsiloxane (PDMS)-based microfluidic devices provide advantages including precise positioning of cells and throughput, however device fabrication is time-consuming and requires specialised skills. Agarose pads are a popular alternative, however cells often clump together, which hinders single cell quantitation. Here, we imprint agarose pads with micro-patterned 'capsules', to trap individual cells and 'lines', to direct cellular growth outwards in a straight line. We implement this micro-patterning into multi-pad devices called CapsuleHotel and LineHotel for high-throughput imaging. CapsuleHotel provides ~65,000 capsule structures per mm

Indexed as

Lab-On-A-Chip DevicesMicroscopyEscherichia coliMicrofluidic Analytical Techniques

Identifiers

PMID29269838
PMCPMC5740163

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.