Evidence map›Paper›PMID 30612540›Full record

ArticleBMC bioinformatics2019

OMeta: an ontology-based, data-driven metadata tracking system.

Indresh Singh, Mehmet Kuscuoglu, Derek M Harkins, Granger Sutton, Derrick E Fouts, Karen E Nelson

Abstract read
In one paragraph

Article in BMC bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
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  7. Antibiotic resistance: Time of synthesis in a post-genomic age.Computational and structural biotechnology journal · 2021
    Review
  8. Review
  9. 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

6 authors.

Indresh SinghJ. Craig Venter Institute, 9605 Medical Center Drive, Suite 150, Rockville, MD, 20850, USA. isingh@jcvi.org.ORCID http://orcid.org/0000-0002-5522-0903
Mehmet KuscuogluJ. Craig Venter Institute, 4120 Capricorn Ln, La Jolla, CA, 92037, USA.
Derek M HarkinsJ. Craig Venter Institute, 9605 Medical Center Drive, Suite 150, Rockville, MD, 20850, USA.
Granger SuttonJ. Craig Venter Institute, 9605 Medical Center Drive, Suite 150, Rockville, MD, 20850, USA.
Derrick E FoutsJ. Craig Venter Institute, 9605 Medical Center Drive, Suite 150, Rockville, MD, 20850, USA.
Karen E NelsonJ. Craig Venter Institute, 9605 Medical Center Drive, Suite 150, Rockville, MD, 20850, USA.

Funding

The J. Craig Venter Institute Genome Center for Infectious DiseasesU19AI110819 · NIAID · J. CRAIG VENTER INSTITUTE, INC. · PI TAN, GENE · 2014 to 2018
$29.7M
National Institute of Allergy and Infectious Diseases HHSN272200900007C,U19AI110819NIAID NIH HHS HHSN272200900007CNIAID NIH HHS U19 AI110819
6 · The paper itself

Abstract

backgroundThe development of high-throughput sequencing and analysis has accelerated multi-omics studies of thousands of microbial species, metagenomes, and infectious disease pathogens. Omics studies are enabling genotype-phenotype association studies which identify genetic determinants of pathogen virulence and drug resistance, as well as phylogenetic studies designed to track the origin and spread of disease outbreaks. These omics studies are complex and often employ multiple assay technologies including genomics, metagenomics, transcriptomics, proteomics, and metabolomics. To maximize the impact of omics studies, it is essential that data be accompanied by detailed contextual metadata (e.g., specimen, spatial-temporal, phenotypic characteristics) in clear, organized, and consistent formats. Over the years, many metadata standards developed by various metadata standards initiatives have arisen; the Genomic Standards Consortium's minimal information standards (MIxS), the GSCID/BRC Project and Sample Application Standard. Some tools exist for tracking metadata, but they do not provide event based capabilities to configure, collect, validate, and distribute metadata. To address this gap in the scientific community, an event based data-driven application, OMeta, was created that allows users to quickly configure, collect, validate, distribute, and integrate metadata.

resultsA data-driven web application, OMeta, has been developed for use by researchers consisting of a browser-based interface, a command-line interface (CLI), and server-side components that provide an intuitive platform for configuring, capturing, viewing, and sharing metadata. Project and sample metadata can be set based on existing standards or based on projects goals. Recorded information includes details on the biological samples, procedures, protocols, and experimental technologies, etc. This information can be organized based on events, including sample collection, sample quantification, sequencing assay, and analysis results. OMeta enables configuration in various presentation types: checkbox, file, drop-box, ontology, and fields can be configured to use the National Center for Biomedical Ontology (NCBO), a biomedical ontology server. Furthermore, OMeta maintains a complete audit trail of all changes made by users and allows metadata export in comma separated value (CSV) format for convenient deposition of data into public databases.

conclusionsWe present, OMeta, a web-based software application that is built on data-driven principles for configuring and customizing data standards, capturing, curating, and sharing metadata.

Indexed as

Biological OntologiesMetadataSoftwareDatabases, FactualMetagenomicsPhylogenyUser-Computer InterfaceWhole Genome SequencingData depositData integrityGenomicsGSC/BRC standardsMetadataMIMSMIxSOntologyStandards

Identifiers

PMID30612540
PMCPMC6322262

What OpenQuestion 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 OpenQuestion graph.