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noisyR: enhancing biological signal in sequencing datasets by characterizing random technical noise.
Moutsopoulos, Ilias; Maischak, Lukas; Lauzikaite, Elze; Vasquez Urbina, Sergio A; Williams, Eleanor C; Drost, Hajk-Georg; Mohorianu, Irina I.
Affiliation
  • Moutsopoulos I; Wellcome-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge CB2 0AW, UK.
  • Maischak L; Computational Biology Group, Department of Molecular Biology, Max Planck Institute for Developmental Biology, Max-Planck Ring 1, 72076 Tübingen, Germany.
  • Lauzikaite E; Wellcome-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge CB2 0AW, UK.
  • Vasquez Urbina SA; Computational Biology Group, Department of Molecular Biology, Max Planck Institute for Developmental Biology, Max-Planck Ring 1, 72076 Tübingen, Germany.
  • Williams EC; Wellcome-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge CB2 0AW, UK.
  • Drost HG; Computational Biology Group, Department of Molecular Biology, Max Planck Institute for Developmental Biology, Max-Planck Ring 1, 72076 Tübingen, Germany.
  • Mohorianu II; Wellcome-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge CB2 0AW, UK.
Nucleic Acids Res ; 49(14): e83, 2021 08 20.
Article in En | MEDLINE | ID: mdl-34076236
High-throughput sequencing enables an unprecedented resolution in transcript quantification, at the cost of magnifying the impact of technical noise. The consistent reduction of random background noise to capture functionally meaningful biological signals is still challenging. Intrinsic sequencing variability introducing low-level expression variations can obscure patterns in downstream analyses. We introduce noisyR, a comprehensive noise filter to assess the variation in signal distribution and achieve an optimal information-consistency across replicates and samples; this selection also facilitates meaningful pattern recognition outside the background-noise range. noisyR is applicable to count matrices and sequencing data; it outputs sample-specific signal/noise thresholds and filtered expression matrices. We exemplify the effects of minimizing technical noise on several datasets, across various sequencing assays: coding, non-coding RNAs and interactions, at bulk and single-cell level. An immediate consequence of filtering out noise is the convergence of predictions (differential-expression calls, enrichment analyses and inference of gene regulatory networks) across different approaches.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Computational Biology / Gene Expression Profiling / Gene Regulatory Networks / Single-Cell Analysis / RNA-Seq Type of study: Clinical_trials / Prognostic_studies Limits: Animals / Humans Language: En Journal: Nucleic Acids Res Year: 2021 Document type: Article Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Computational Biology / Gene Expression Profiling / Gene Regulatory Networks / Single-Cell Analysis / RNA-Seq Type of study: Clinical_trials / Prognostic_studies Limits: Animals / Humans Language: En Journal: Nucleic Acids Res Year: 2021 Document type: Article Country of publication: United kingdom