Evidence map›Paper›PMID 26743993›Full record

ArticleNeuroinformatics2016

Adaptive and Background-Aware GAL4 Expression Enhancement of Co-registered Confocal Microscopy Images.

Martin Trapp, Florian Schulze, Alexey A Novikov, Laszlo Tirian, Barry J Dickson, Katja Bühler

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Article in Neuroinformatics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Martin TrappVRVis Center for Virtual Reality and Visualization, Vienna, Austria.
Florian SchulzeVRVis Center for Virtual Reality and Visualization, Vienna, Austria. fschulze@vrvis.at.
Alexey A NovikovVRVis Center for Virtual Reality and Visualization, Vienna, Austria.
Laszlo TirianResearch Institute of Molecular Pathology, Vienna, Austria.
Barry J DicksonJanelia Research Campus, Ashburn, VA, USA.
Katja BühlerVRVis Center for Virtual Reality and Visualization, Vienna, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

GAL4 gene expression imaging using confocal microscopy is a common and powerful technique used to study the nervous system of a model organism such as Drosophila melanogaster. Recent research projects focused on high throughput screenings of thousands of different driver lines, resulting in large image databases. The amount of data generated makes manual assessment tedious or even impossible. The first and most important step in any automatic image processing and data extraction pipeline is to enhance areas with relevant signal. However, data acquired via high throughput imaging tends to be less then ideal for this task, often showing high amounts of background signal. Furthermore, neuronal structures and in particular thin and elongated projections with a weak staining signal are easily lost. In this paper we present a method for enhancing the relevant signal by utilizing a Hessian-based filter to augment thin and weak tube-like structures in the image. To get optimal results, we present a novel adaptive background-aware enhancement filter parametrized with the local background intensity, which is estimated based on a common background model. We also integrate recent research on adaptive image enhancement into our approach, allowing us to propose an effective solution for known problems present in confocal microscopy images. We provide an evaluation based on annotated image data and compare our results against current state-of-the-art algorithms. The results show that our algorithm clearly outperforms the existing solutions.

Indexed as

Image Processing, Computer-AssistedMicroscopy, ConfocalAlgorithmsAnimalsDrosophila melanogasterDrosophila ProteinsHumansModels, NeurologicalNeuronsPattern Recognition, AutomatedTranscription FactorsDrosophila ProteinsGAL4 protein, DrosophilaTranscription FactorsAdaptive image enhancementBackground-awareBrainGazerConfocal microscopyDrosophilaGAL4 enhancementNeuron

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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.