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FIRE: functional inference of genetic variants that regulate gene expression.
Ioannidis, Nilah M; Davis, Joe R; DeGorter, Marianne K; Larson, Nicholas B; McDonnell, Shannon K; French, Amy J; Battle, Alexis J; Hastie, Trevor J; Thibodeau, Stephen N; Montgomery, Stephen B; Bustamante, Carlos D; Sieh, Weiva; Whittemore, Alice S.
Afiliación
  • Ioannidis NM; Department of Genetics.
  • Davis JR; Department of Health Research & Policy.
  • DeGorter MK; Department of Genetics.
  • Larson NB; Department of Genetics.
  • McDonnell SK; Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • French AJ; Department of Health Sciences Research.
  • Battle AJ; Department of Health Sciences Research.
  • Hastie TJ; Department of Laboratory Medicine & Pathology, Mayo Clinic, Rochester, MN 55905, USA.
  • Thibodeau SN; Department of Computer Science, Johns Hopkins University, Baltimore, MD 21218, USA.
  • Montgomery SB; Department of Statistics, Stanford University, Stanford, CA 94305, USA.
  • Bustamante CD; Department of Biomedical Data Science, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Sieh W; Department of Laboratory Medicine & Pathology, Mayo Clinic, Rochester, MN 55905, USA.
  • Whittemore AS; Department of Genetics.
Bioinformatics ; 33(24): 3895-3901, 2017 Dec 15.
Article en En | MEDLINE | ID: mdl-28961785
MOTIVATION: Interpreting genetic variation in noncoding regions of the genome is an important challenge for personal genome analysis. One mechanism by which noncoding single nucleotide variants (SNVs) influence downstream phenotypes is through the regulation of gene expression. Methods to predict whether or not individual SNVs are likely to regulate gene expression would aid interpretation of variants of unknown significance identified in whole-genome sequencing studies. RESULTS: We developed FIRE (Functional Inference of Regulators of Expression), a tool to score both noncoding and coding SNVs based on their potential to regulate the expression levels of nearby genes. FIRE consists of 23 random forests trained to recognize SNVs in cis-expression quantitative trait loci (cis-eQTLs) using a set of 92 genomic annotations as predictive features. FIRE scores discriminate cis-eQTL SNVs from non-eQTL SNVs in the training set with a cross-validated area under the receiver operating characteristic curve (AUC) of 0.807, and discriminate cis-eQTL SNVs shared across six populations of different ancestry from non-eQTL SNVs with an AUC of 0.939. FIRE scores are also predictive of cis-eQTL SNVs across a variety of tissue types. AVAILABILITY AND IMPLEMENTATION: FIRE scores for genome-wide SNVs in hg19/GRCh37 are available for download at https://sites.google.com/site/fireregulatoryvariation/. CONTACT: nilah@stanford.edu. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Variación Genética / Programas Informáticos / Regulación de la Expresión Génica Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Bioinformatics Asunto de la revista: INFORMATICA MEDICA Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Variación Genética / Programas Informáticos / Regulación de la Expresión Génica Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Bioinformatics Asunto de la revista: INFORMATICA MEDICA Año: 2017 Tipo del documento: Article
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