bioRxivPhysiologyPreprint
Deconvoluting fiber type proportions from human skeletal muscle transcriptomics and proteomics data using FibeRtypeR
Thibaux Van der StedeiD, Roger Moreno‐JusticiaiD, Freek Van de CasteeleiD, Eline LievensiD, Alexia Van de LoockiD, Jonas VandecauteriD, Peter MerseburgeriD, Jimmy Van den EyndeniD, Delphi Van HaveriD, An StaesiD, Simon DevosiD, Morten HostrupiD, Pieter MestdaghiD, Jo VandesompeleiD, Ben StocksiD, Atul S. DeshmukhiD, Wim DeraveiD
Abstract
Muscle fibers are the dominant, multinucleated cell type in skeletal muscle. In humans, they can be classified as slow (type 1) and fast (type 2) fibers, traditionally based on distinct properties of their contractile machinery. Slow and fast fibers are characterized by shared and specific cellular complexities that are pivotal for their adaptive capacity to exercise or role in metabolic disease progression. In this era of omics research, there is a critical need to accurately infer muscle fiber type proportions from bulk tissue omics datasets, as single-fiber approaches are not feasible in large-scale or retrospective studies. Here we present FibeRtypeR, an easy-to-use web application to accurately estimate fiber type proportions from bulk transcriptomics and proteomics datasets: https://muscleapps.ugent.be. FibeRtypeR exploits transcriptomics and proteomics profiles of 1000 fiber-typed individual human skeletal muscle fibers as a reference dataset and is validated against paired immunohistochemical fiber type determinations in 160 muscle biopsies. We show that FibeRtypeR can be applied to public datasets, illustrating the application potential across a wide range of biological contexts such as aging, disease and exercise training. This new freely accessible computational tool will prove valuable to the skeletal muscle research community. Key pointsO_LIBulk muscle omics datasets lack fiber type specific information C_LIO_LIOur new tool, FibeRtypeR, leverages in-house collected single-fiber profiles allowing for accurate fiber type inference C_LIO_LIFibeRtypeR is methodologically robust across omics technologies and workflows C_LIO_LIWe host FibeRtypeR as an intuitive open-access Shiny app, applicable to new and publicly available transcriptomics and proteomics datasets C_LI
- organism: human
- assay: bulk RNA-seq
- assay: proteomics
- research focus: cell type annotation
- research focus: differential expression
- research focus: deconvolution
- approach: deep learning
- approach: statistical model
- Citations
- 3
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