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OUTRIDER: A Statistical Method for Detecting Aberrantly Expressed Genes in RNA Sequencing Data.
Brechtmann, Felix; Mertes, Christian; Matuseviciute, Agne; Yépez, Vicente A; Avsec, Ziga; Herzog, Maximilian; Bader, Daniel M; Prokisch, Holger; Gagneur, Julien.
Afiliação
  • Brechtmann F; Department of Informatics, Technical University of Munich, Boltzmannstr. 3, 85748 Garching, Germany.
  • Mertes C; Department of Informatics, Technical University of Munich, Boltzmannstr. 3, 85748 Garching, Germany.
  • Matuseviciute A; Department of Informatics, Technical University of Munich, Boltzmannstr. 3, 85748 Garching, Germany.
  • Yépez VA; Department of Informatics, Technical University of Munich, Boltzmannstr. 3, 85748 Garching, Germany; Quantitative Biosciences Munich, Gene Center, Department of Biochemistry, Ludwig-Maximilians Universität München, Feodor-Lynen-Str. 25, 81377 München, Germany.
  • Avsec Z; Department of Informatics, Technical University of Munich, Boltzmannstr. 3, 85748 Garching, Germany; Quantitative Biosciences Munich, Gene Center, Department of Biochemistry, Ludwig-Maximilians Universität München, Feodor-Lynen-Str. 25, 81377 München, Germany.
  • Herzog M; Department of Informatics, Technical University of Munich, Boltzmannstr. 3, 85748 Garching, Germany.
  • Bader DM; Department of Informatics, Technical University of Munich, Boltzmannstr. 3, 85748 Garching, Germany.
  • Prokisch H; Institute of Human Genetics, Helmholtz Zentrum München, Ingolstädter Landstr. 1, 85764 Neuherberg, Germany; Institute of Human Genetics, Klinikum rechts der Isar, Technical University of Munich, 13 Ismaninger Str. 22, 81675 München, Germany.
  • Gagneur J; Department of Informatics, Technical University of Munich, Boltzmannstr. 3, 85748 Garching, Germany; Quantitative Biosciences Munich, Gene Center, Department of Biochemistry, Ludwig-Maximilians Universität München, Feodor-Lynen-Str. 25, 81377 München, Germany. Electronic address: gagneur@in.tum.de.
Am J Hum Genet ; 103(6): 907-917, 2018 12 06.
Article em En | MEDLINE | ID: mdl-30503520
ABSTRACT
RNA sequencing (RNA-seq) is gaining popularity as a complementary assay to genome sequencing for precisely identifying the molecular causes of rare disorders. A powerful approach is to identify aberrant gene expression levels as potential pathogenic events. However, existing methods for detecting aberrant read counts in RNA-seq data either lack assessments of statistical significance, so that establishing cutoffs is arbitrary, or rely on subjective manual corrections for confounders. Here, we describe OUTRIDER (Outlier in RNA-Seq Finder), an algorithm developed to address these issues. The algorithm uses an autoencoder to model read-count expectations according to the gene covariation resulting from technical, environmental, or common genetic variations. Given these expectations, the RNA-seq read counts are assumed to follow a negative binomial distribution with a gene-specific dispersion. Outliers are then identified as read counts that significantly deviate from this distribution. The model is automatically fitted to achieve the best recall of artificially corrupted data. Precision-recall analyses using simulated outlier read counts demonstrated the importance of controlling for covariation and significance-based thresholds. OUTRIDER is open source and includes functions for filtering out genes not expressed in a dataset, for identifying outlier samples with too many aberrantly expressed genes, and for detecting aberrant gene expression on the basis of false-discovery-rate-adjusted p values. Overall, OUTRIDER provides an end-to-end solution for identifying aberrantly expressed genes and is suitable for use by rare-disease diagnostic platforms.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / RNA / Expressão Gênica / Análise de Sequência de RNA Tipo de estudo: Guideline Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / RNA / Expressão Gênica / Análise de Sequência de RNA Tipo de estudo: Guideline Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article