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AbstractMotivationInconsistent, analytical noise introduced either by the sequencing technology or by the choice of read-processing tools can bias bulk RNA-seq analyses by shifting the focus to the variation in expression of low-abundance transcripts; as a consequence these highly-variable genes are often included the differential expression (DE) call and impact the interpretation of results.ResultsTo illustrate the effects of “noise”, we present simulated datasets following closely the characteristics of a H.sapiens and a M.musculus dataset, respectively, highlighting the extent of technical-noise in both a high inter-individual variability (H. sapiens) and reduced variability (M. Musculus) setup. The sequencing-induced noise is assessed using correlations of distributions of expression across transcripts; analytical noise is evaluated through side-by-side comparisons of several standard choices. The proportion of genes in the noise-range differs for each tool combi-nation. Data-driven, sample-specific noise-thresholds were applied to reduce the impact of low-level variation. Noise-adjustment reduced the number of significantly DE genes and gave rise to convergent calls across tool combinations.AvailabilityThe code for determining the sequence-derived noise is available for download from: https://github.com/yry/noiseAnalysis/tree/master/noiseDetection_mRNA; the code for running the analysis is available for download from: https://github.com/sheerind/noise_detection.

Original publication

DOI

10.1101/843789

Type

Journal article

Publication Date

16/11/2019