Evidence map›Paper›PMID 24069313›Full record

ArticlePloS one2013

An automated microfluidic multiplexer for fast delivery of C. elegans populations from multiwells.

Navid Ghorashian, Sertan Kutal Gökçe, Sam Xun Guo, William Neil Everett, Adela Ben-Yakar

Abstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Planar Laser Activated Neuronal Scanning (PLANS) System forFrontiers in optics. Annual Meeting of the Optical Society of America · 2020
    Article
  2. Review
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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

5 authors.

Navid GhorashianBiomedical Engineering, University of Texas, Austin, Texas, United States of America.
Sertan Kutal Gökçe
Sam Xun Guo
William Neil Everett
Adela Ben-Yakar

Funding

High-speed opto-fluidics to screen entire nervous system in aging and diseaseR01AG041135 · NIA · UNIVERSITY OF TEXAS AT AUSTIN · PI BEN-YAKAR, ADELA, PIERCE, JONATHAN THOMAS · 2011 to 2015
$2.8M
Femtosecond laser axotomy for in vivo nerve regeneration studies in C elegansR01NS060129 · NINDS · UNIVERSITY OF TEXAS AT AUSTIN · PI BEN-YAKAR, ADELA · 2007 to 2010
$1.7M
Microfluidic-microtiter interface for rapid large-scale screenings of C. elegansR21NS067340 · NINDS · UNIVERSITY OF TEXAS AT AUSTIN · PI BEN-YAKAR, ADELA · 2009 to 2010
$409k
NIA NIH HHS R01 AG041135NINDS NIH HHS R01 NS060129NINDS NIH HHS R21 NS067340
6 · The paper itself

Abstract

Automated biosorter platforms, including recently developed microfluidic devices, enable and accelerate high-throughput and/or high-resolution bioassays on small animal models. However, time-consuming delivery of different organism populations to these systems introduces a major bottleneck to executing large-scale screens. Current population delivery strategies rely on suction from conventional well plates through tubing periodically exposed to air, leading to certain disadvantages: 1) bubble introduction to the sample, interfering with analysis in the downstream system, 2) substantial time drain from added bubble-cleaning steps, and 3) the need for complex mechanical systems to manipulate well plate position. To address these concerns, we developed a multiwell-format microfluidic platform that can deliver multiple distinct animal populations from on-chip wells using multiplexed valve control. This Population Delivery Chip could operate autonomously as part of a relatively simple setup that did not require any of the major mechanical moving parts typical of plate-handling systems to address a given well. We demonstrated automatic serial delivery of 16 distinct C. elegans worm populations to a single outlet without introducing any bubbles to the samples, causing cross-contamination, or damaging the animals. The device achieved delivery of more than 90% of the population preloaded into a given well in 4.7 seconds; an order of magnitude faster than delivery modalities in current use. This platform could potentially handle other similarly sized model organisms, such as zebrafish and drosophila larvae or cellular micro-colonies. The device's architecture and microchannel dimensions allow simple expansion for processing larger numbers of populations.

Indexed as

Caenorhabditis elegansAnimalsHigh-Throughput Nucleotide SequencingMicrofluidic Analytical TechniquesReproducibility of ResultsSpecimen Handling

Identifiers

PMID24069313
PMCPMC3775957

What OpenQuestion holds

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LicenceCC BY
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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.