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Stanley E. Lazic

dblp:209/7178 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2017
—ORCID · unresolved

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 2 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › bioimage informatics
cellular image analysis
0.312017
A multi-scale convolutional neural network for phenotyping high-content cellular images · Bioinform. 2017
Bioinformatics and computational biology
phenotype classification
0.312017
A multi-scale convolutional neural network for phenotyping high-content cellular images · Bioinform. 2017

Methods — techniques the papers use, named apart from their topics

multi-scale convolutional neural network · 0.3
YearPublicationVenuePosition
2017 A multi-scale convolutional neural network for phenotyping high-content cellular images
abstract
MOTIVATION: Identifying phenotypes based on high-content cellular images is challenging. Conventional image analysis pipelines for phenotype identification comprise multiple independent steps, with each step requiring method customization and adjustment of multiple parameters. RESULTS: Here, we present an approach based on a multi-scale convolutional neural network (M-CNN) that classifies, in a single cohesive step, cellular images into phenotypes by using directly and solely the images' pixel intensity values. The only parameters in the approach are the weights of the neural network, which are automatically optimized based on training images. The approach requires no a priori knowledge or manual customization, and is applicable to single- or multi-channel images displaying single or multiple cells. We evaluated the classification performance of the approach on eight diverse benchmark datasets. The approach yielded overall a higher classification accuracy compared with state-of-the-art results, including those of other deep CNN architectures. In addition to using the network to simply obtain a yes-or-no prediction for a given phenotype, we use the probability outputs calculated by the network to quantitatively describe the phenotypes. This study shows that these probability values correlate with chemical treatment concentrations. This finding validates further our approach and enables chemical treatment potency estimation via CNNs. AVAILABILITY AND IMPLEMENTATION: The network specifications and solver definitions are provided in Supplementary Software 1. CONTACT: [email protected] or [email protected]. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
William J. Godinez, Imtiaz Hossain, Stanley E. Lazic, John W. Davies, Xian Zhang 0004
Bioinform.3