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TIGA: target illumination GWAS analytics.
Yang, Jeremy J; Grissa, Dhouha; Lambert, Christophe G; Bologa, Cristian G; Mathias, Stephen L; Waller, Anna; Wild, David J; Jensen, Lars Juhl; Oprea, Tudor I.
Afiliação
  • Yang JJ; Division of Translational Informatics, Department of Internal Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA.
  • Grissa D; Integrative Data Science Laboratory, School of Informatics, Computing and Engineering, Indiana University, Bloomington, IN 47408, USA.
  • Lambert CG; Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen 2200, Denmark.
  • Bologa CG; Division of Translational Informatics, Department of Internal Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA.
  • Mathias SL; Division of Translational Informatics, Department of Internal Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA.
  • Waller A; Division of Translational Informatics, Department of Internal Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA.
  • Wild DJ; Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA.
  • Jensen LJ; Integrative Data Science Laboratory, School of Informatics, Computing and Engineering, Indiana University, Bloomington, IN 47408, USA.
  • Oprea TI; Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen 2200, Denmark.
Bioinformatics ; 37(21): 3865-3873, 2021 11 05.
Article em En | MEDLINE | ID: mdl-34086846
ABSTRACT
MOTIVATION Genome-wide association studies can reveal important genotype-phenotype associations; however, data quality and interpretability issues must be addressed. For drug discovery scientists seeking to prioritize targets based on the available evidence, these issues go beyond the single study.

RESULTS:

Here, we describe rational ranking, filtering and interpretation of inferred gene-trait associations and data aggregation across studies by leveraging existing curation and harmonization efforts. Each gene-trait association is evaluated for confidence, with scores derived solely from aggregated statistics, linking a protein-coding gene and phenotype. We propose a method for assessing confidence in gene-trait associations from evidence aggregated across studies, including a bibliometric assessment of scientific consensus based on the iCite relative citation ratio, and meanRank scores, to aggregate multivariate evidence.This method, intended for drug target hypothesis generation, scoring and ranking, has been implemented as an analytical pipeline, available as open source, with public datasets of results, and a web application designed for usability by drug discovery scientists. AVAILABILITY AND IMPLEMENTATION Web application, datasets and source code via https//unmtid-shinyapps.net/tiga/. SUPPLEMENTARY INFORMATION Supplementary data are available at Bioinformatics online.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Iluminação / Estudo de Associação Genômica Ampla Idioma: En Revista: Bioinformatics Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Iluminação / Estudo de Associação Genômica Ampla Idioma: En Revista: Bioinformatics Ano de publicação: 2021 Tipo de documento: Article