Evidence map›Paper›PMID 33553865›Full record

ArticleACS omega2021

ChipSeg: An Automatic Tool to Segment Bacterial and Mammalian Cells Cultured in Microfluidic Devices.

Irene de Cesare, Criseida G Zamora-Chimal, Lorena Postiglione, Mahmoud Khazim, Elisa Pedone, Barbara Shannon, Gianfranco Fiore, Giansimone Perrino, Sara Napolitano, Diego di Bernardo and 4 more

Open access · goldAbstract read
In one paragraph

Article in ACS omega, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
4.5field-weighted citation impact, top 6% of its field
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

7 citing papers in PubMed, 23 citations in OpenAlex.

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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

14 authors at 2 institutions in 2 countries.

Irene de CesareDepartment of Engineering Mathematics, University of Bristol, Woodland Road, Bristol BS8 1UB, U.K.
Criseida G Zamora-ChimalDepartment of Engineering Mathematics, University of Bristol, Woodland Road, Bristol BS8 1UB, U.K.
Lorena PostiglioneDepartment of Engineering Mathematics, University of Bristol, Woodland Road, Bristol BS8 1UB, U.K.
Mahmoud KhazimDepartment of Engineering Mathematics, University of Bristol, Woodland Road, Bristol BS8 1UB, U.K.
Elisa PedoneDepartment of Engineering Mathematics, University of Bristol, Woodland Road, Bristol BS8 1UB, U.K.
Barbara ShannonBrisSynBio, Life Sciences Building, University of Bristol, Tyndall Avenue, Bristol BS8 1TQ, U.K.
Gianfranco FioreDepartment of Engineering Mathematics, University of Bristol, Woodland Road, Bristol BS8 1UB, U.K.
Giansimone PerrinoTelethon Institute of Genetic and Medicine Via Campi Flegrei 34, 80078 Pozzuoli, Italy.
Sara NapolitanoTelethon Institute of Genetic and Medicine Via Campi Flegrei 34, 80078 Pozzuoli, Italy.
Diego di BernardoTelethon Institute of Genetic and Medicine Via Campi Flegrei 34, 80078 Pozzuoli, Italy.
Nigel J SaveryBrisSynBio, Life Sciences Building, University of Bristol, Tyndall Avenue, Bristol BS8 1TQ, U.K.
Claire GriersonBrisSynBio, Life Sciences Building, University of Bristol, Tyndall Avenue, Bristol BS8 1TQ, U.K.
Mario di BernardoDepartment of Engineering Mathematics, University of Bristol, Woodland Road, Bristol BS8 1UB, U.K.
Lucia MarucciDepartment of Engineering Mathematics, University of Bristol, Woodland Road, Bristol BS8 1UB, U.K.
University of Bristol · GBTelethon Institute Of Genetics And Medicine · IT

Funding

Biotechnology and Biological Sciences Research Council BB/L01386X/1Medical Research Council MR/N021444/1
6 · The paper itself

Abstract

Extracting quantitative measurements from time-lapse images is necessary in external feedback control applications, where segmentation results are used to inform control algorithms. We describe ChipSeg, a computational tool that segments bacterial and mammalian cells cultured in microfluidic devices and imaged by time-lapse microscopy, which can be used also in the context of external feedback control. The method is based on thresholding and uses the same core functions for both cell types. It allows us to segment individual cells in high cell density microfluidic devices, to quantify fluorescent protein expression over a time-lapse experiment, and to track individual mammalian cells. ChipSeg enables robust segmentation in external feedback control experiments and can be easily customized for other experimental settings and research aims.

Identifiers

PMID33553865
PMCPMC7859942
OpenAlexW3111664956

What OpenQuestion holds

Textmetadata
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.