Evidence map›Paper›PMID 26427464›Full record

ArticleAdvances in experimental medicine and biology2016

Use of a Machine Learning-Based High Content Analysis Approach to Identify Photoreceptor Neurite Promoting Molecules.

John A Fuller, Cynthia A Berlinicke, James Inglese, Donald J Zack

Abstract read
In one paragraph

Article in Advances in experimental medicine and biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 10% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. Article
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 at 2 institutions in 1 country.

John A FullerOphthalmology, Molecular Biology & Genetics, Neuroscience, and Institute of Genetic Medicine, Wilmer Eye Institute, Johns Hopkins University School of Medicine, 400 N Broadway, Smith 3001, 21231, Baltimore, MD, USA. jfulle19@jhmi.edu.
Cynthia A BerlinickeOphthalmology, Molecular Biology & Genetics, Neuroscience, and Institute of Genetic Medicine, Wilmer Eye Institute, Johns Hopkins University School of Medicine, 400 N Broadway, Smith 3001, 21231, Baltimore, MD, USA. cdoughe1@jhmi.edu.
James IngleseNCATS, NHGRI, National Institutes of Health, 9800 Medical Center Drive, MSC 3370, 20850, Rockville, MD, USA. jinglese@mail.nih.gov.
Donald J ZackOphthalmology, Molecular Biology & Genetics, Neuroscience, and Institute of Genetic Medicine, Wilmer Eye Institute, Johns Hopkins University School of Medicine, 400 N Broadway, Smith 3001, 21231, Baltimore, MD, USA. donzack@gmail.com.
Johns Hopkins University · USNational Center for Advancing Translational Sciences · US

Funding

Small molecule screening programZ01HG200319 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI AUSTIN, CHRISTOPHER P · 2004 to 2008
$32.3M
A High Content Screening Approach for the Retinal Degenerative DiseasesR01EY024249 · NEI · JOHNS HOPKINS UNIVERSITY · PI BERLINICKE, CYNTHIA · 2015 to 2019
$2.0M
Intramural NIH HHS Z01 HG200319NEI NIH HHS R01 EY024249
6 · The paper itself

Abstract

High content analysis (HCA) has become a leading methodology in phenotypic drug discovery efforts. Typical HCA workflows include imaging cells using an automated microscope and analyzing the data using algorithms designed to quantify one or more specific phenotypes of interest. Due to the richness of high content data, unappreciated phenotypic changes may be discovered in existing image sets using interactive machine-learning based software systems. Primary postnatal day four retinal cells from the photoreceptor (PR) labeled QRX-EGFP reporter mice were isolated, seeded, treated with a set of 234 profiled kinase inhibitors and then cultured for 1 week. The cells were imaged with an Acumen plate-based laser cytometer to determine the number and intensity of GFP-expressing, i.e. PR, cells. Wells displaying intensities and counts above threshold values of interest were re-imaged at a higher resolution with an INCell2000 automated microscope. The images were analyzed with an open source HCA analysis tool, PhenoRipper (Rajaram et al., Nat Methods 9:635-637, 2012), to identify the high GFP-inducing treatments that additionally resulted in diverse phenotypes compared to the vehicle control samples. The pyrimidinopyrimidone kinase inhibitor CHEMBL-1766490, a pan kinase inhibitor whose major known targets are p38α and the Src family member lck, was identified as an inducer of photoreceptor neuritogenesis by using the open-source HCA program PhenoRipper. This finding was corroborated using a cell-based method of image analysis that measures quantitative differences in the mean neurite length in GFP expressing cells. Interacting with data using machine learning algorithms may complement traditional HCA approaches by leading to the discovery of small molecule-induced cellular phenotypes in addition to those upon which the investigator is initially focusing.

Indexed as

AlgorithmsMachine LearningAnimalsCells, CulturedCell TrackingComputational BiologyEnzyme InhibitorsGreen Fluorescent ProteinsMice, TransgenicNeuritesPhosphotransferasesPhotoreceptor Cells, VertebratePrimary Cell CultureReproducibility of ResultsSmall Molecule LibrariesEnzyme InhibitorsGreen Fluorescent ProteinsPhosphotransferasesSmall Molecule LibrariesHigh content analysisImagingInhibitorMachine learningNeuritogenesisPhenotypic screeningPhotoreceptorProtein kinaseqHTS

Identifiers

PMID26427464
PMCPMC5815518
OpenAlexW2399203513

What OpenQuestion holds

Textmetadata
LicenceTDM
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.