Evidence map›Paper›PMID 31188086›Full record

ArticleZebrafish2019

Development of a Zebrafish S1500+ Sentinel Gene Set for High-Throughput Transcriptomics.

Michele R Balik-Meisner, Deepak Mav, Dhiral P Phadke, Logan J Everett, Ruchir R Shah, Tamara Tal, Peter J Shepard, B Alex Merrick, Richard S Paules

Open access · hybridAbstract read
In one paragraph

Article in Zebrafish, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

8 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
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  4. Review
  5. Review
  6. Article
  7. Review
  8. Translational Toxicology in Zebrafish.Current opinion in toxicology
    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

9 authors at 4 institutions in 1 country.

Michele R Balik-Meisner1Sciome, LLC, Research Triangle Park, North Carolina.
Deepak Mav1Sciome, LLC, Research Triangle Park, North Carolina.
Dhiral P Phadke1Sciome, LLC, Research Triangle Park, North Carolina.
Logan J Everett1Sciome, LLC, Research Triangle Park, North Carolina.
Ruchir R Shah1Sciome, LLC, Research Triangle Park, North Carolina.
Tamara Tal2National Health and Environmental Effects Research Laboratory, Office of Research and Development, U.S. Environmental Protection Agency, Research Triangle Park, North Carolina.
Peter J Shepard3BioSpyder Technologies, Incorporated, Carlsbad, California.
B Alex Merrick4Division of the National Toxicology Program, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina.
Richard S Paules4Division of the National Toxicology Program, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina.
Research Triangle Park Foundation · USNational Institute of Environmental Health Sciences · USBiospyder (United States) · USEnvironmental Protection Agency · US

Funding

Biomolecular Screening and Alternative Approaches for the National Toxicology ProgramZIAES103318 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI CASEY, WARREN · 2016 to 2021
$25.0M
Intramural NIH HHS ZIA ES103318NIEHS NIH HHS HHSN273201700001C
6 · The paper itself

Abstract

Sentinel gene sets have been developed with the purpose of maximizing the information from targeted transcriptomic platforms. We recently described the development of an S1500+ sentinel gene set, which was built for the human transcriptome, utilizing a data- and knowledge-driven hybrid approach to select a small subset of genes that optimally capture transcriptional diversity, correlation with other genes based on large-scale expression profiling, and known pathway annotation within the human genome. While this detailed bioinformatics approach for gene selection can in principle be applied to other species, the reliability of the resulting gene set depends on availability of a large body of transcriptomics data. For the model organism zebrafish, we aimed to create a similar sentinel gene set (Zf S1500+ gene set); however, there is insufficient standardized expression data in the public domain to train the gene correlation model. Therefore, our strategy was to use human-zebrafish ortholog mapping of the human S1500+ genes and nominations from experts in the zebrafish scientific community. In this study, we present the bioinformatics curation and refinement process to produce the final Zf S1500+ gene set, explore whole transcriptome extrapolation using this gene set, and assess pathway-level inference. This gene set will add value to targeted high-throughput transcriptomics in zebrafish for toxicogenomic screening and other research domains.

Indexed as

High-Throughput Nucleotide SequencingTranscriptomeAnimalsComputational BiologyDatabases, GeneticGene Expression ProfilingReproducibility of ResultsZebrafishS1500S1500+transcriptomicszebrafish

Identifiers

PMID31188086
PMCPMC6685209
OpenAlexW2952500998

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.