Found: 28
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An explainable artificial intelligence approach for predicting cardiovascular outcomes using electronic health records.
- Published in:
- PLoS Digital Health, 2022, v. 1, n. 1, p. 1, doi. 10.1371/journal.pdig.0000004
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- Article
A Proposed Clinical Decision Support Architecture Capable of Supporting Whole Genome Sequence Information.
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- Journal of Personalized Medicine, 2014, v. 4, n. 2, p. 176, doi. 10.3390/jpm4020176
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- Article
SOBA: sequence ontology bioinformatics analysis.
- Published in:
- Nucleic Acids Research, 2010, v. 38, n. suppl_2, p. W161, doi. 10.1093/nar/gkq426
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- Article
An artificial intelligence approach for investigating multifactorial pain-related features of endometriosis.
- Published in:
- PLoS ONE, 2024, v. 19, n. 2, p. 1, doi. 10.1371/journal.pone.0297998
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- Article
The OBO Foundry: coordinated evolution of ontologies to support biomedical data integration.
- Published in:
- Nature Biotechnology, 2007, v. 25, n. 11, p. 1251, doi. 10.1038/nbt1346
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- Publication type:
- Article
The Non-Coding RNA Ontology (NCRO): a comprehensive resource for the unification of non-coding RNA biology.
- Published in:
- Journal of Biomedical Semantics, 2016, v. 7, p. 1, doi. 10.1186/s13326-016-0066-0
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- Article
OmniSearch: a semantic search system based on the Ontology for MIcroRNA Target (OMIT) for microRNA-target gene interaction data.
- Published in:
- Journal of Biomedical Semantics, 2016, v. 7, p. 1, doi. 10.1186/s13326-016-0064-2
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- Article
Improving the Sequence Ontology terminology for genomic variant annotation.
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- Journal of Biomedical Semantics, 2015, v. 6, n. 1, p. 1, doi. 10.1186/s13326-015-0030-4
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- Article
OMIT: Dynamic, Semi-Automated Ontology Development for the microRNA Domain.
- Published in:
- PLoS ONE, 2014, v. 9, n. 7, p. 1, doi. 10.1371/journal.pone.0100855
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- Publication type:
- Article
Standard Vocabularies to Improve Machine Learning Model Transferability With Electronic Health Record Data: Retrospective Cohort Study Using Health Care--Associated Infection.
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- JMIR Medical Informatics, 2022, v. 10, n. 8, p. 1, doi. 10.2196/39057
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- Article
4549 Reproducible Informatics for Reproducible Translational Research.
- Published in:
- 2020
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- Abstract
3339 Development of a Competency-based Informatics Course for Translational Researchers.
- Published in:
- 2019
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- Publication type:
- Abstract
3399 Systematically Integrating Microbiomes and Exposomes for Translational Research.
- Published in:
- 2019
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- Publication type:
- Abstract
Pain points in parents' interactions with newborn screening systems: a qualitative study.
- Published in:
- 2022
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- Publication type:
- journal article
Quantitative measures for the management and comparison of annotated genomes.
- Published in:
- BMC Bioinformatics, 2009, v. 10, p. 1, doi. 10.1186/1471-2105-10-67
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- Publication type:
- Article
The Business Process Management for Healthcare (BPM+ Health) Consortium: motivation, methodology, and deliverables for enabling clinical knowledge interoperability (CKI).
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- Journal of the American Medical Informatics Association, 2024, v. 31, n. 4, p. 797, doi. 10.1093/jamia/ocad242
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- Publication type:
- Article
Birth of identity: understanding changes to birth certificates and their value for identity resolution.
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- Journal of the American Medical Informatics Association, 2015, v. 22, n. e1, p. e120, doi. 10.1136/amiajnl-2014-002774
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- Publication type:
- Article
Taxonomer: an interactive metagenomics analysis portal for universal pathogen detection and host mRNA expression profiling.
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- Genome Biology, 2016, v. 17, p. 1, doi. 10.1186/s13059-016-0969-1
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- Article
Conceptual modelling of genomic information.
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- Bioinformatics, 2000, v. 16, n. 6, p. 548, doi. 10.1093/bioinformatics/16.6.548
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- Publication type:
- Article
The VAAST Variant Prioritizer (VVP): ultrafast, easy to use whole genome variant prioritization tool.
- Published in:
- BMC Bioinformatics, 2018, v. 19, p. 1, doi. 10.1186/s12859-018-2056-y
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- Publication type:
- Article
Cover Image, Volume 39, Issue 11.
- Published in:
- Human Mutation, 2018, v. 39, n. 11, p. i, doi. 10.1002/humu.23662
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- Publication type:
- Article
Unique aspects of sequence variant interpretation for inborn errors of metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase Gene.
- Published in:
- Human Mutation, 2018, v. 39, n. 11, p. 1569, doi. 10.1002/humu.23649
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- Publication type:
- Article
ClinVar Miner: Demonstrating utility of a Web‐based tool for viewing and filtering ClinVar data.
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- Human Mutation, 2018, v. 39, n. 8, p. 1051, doi. 10.1002/humu.23555
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- Publication type:
- Article
Novel sequence feature variant type analysis of the HLA genetic association in systemic sclerosis.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 4, p. 707, doi. 10.1093/hmg/ddp521
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- Publication type:
- Article
Human Bocavirus Capsid Messenger RNA Detection in Children With Pneumonia.
- Published in:
- 2017
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- Publication type:
- journal article
Viral Pathogen Detection by Metagenomics and Pan-Viral Group Polymerase Chain Reaction in Children With Pneumonia Lacking Identifiable Etiology.
- Published in:
- 2017
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- Publication type:
- journal article
Unification of miRNA and isomiR research: the mirGFF3 format and the mirtop API.
- Published in:
- Bioinformatics, 2020, v. 36, n. 3, p. 698, doi. 10.1093/bioinformatics/btz675
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- Publication type:
- Article
The Protein Feature Ontology: a tool for the unification of protein feature annotations.
- Published in:
- Bioinformatics, 2008, v. 24, n. 23, p. 2767, doi. 10.1093/bioinformatics/btn528
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- Publication type:
- Article