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We present a generative statistical model and associated inference methods that handle read mapping uncertainty in a principled manner. Through simulations parameterized by real RNA-Seq data, we show that our method is more accurate than previous methods. Our improved accuracy is the result of handling read mapping uncertainty with a statistical model and the estimation of gene expression levels as the sum of isoform expression levels. Unlike previous methods, our method is capable of modeling non-uniform read distributions. Simulations with our method indicate that a read length of 20-25 bases is optimal for gene-level expression estimation from mouse and maize RNA-Seq data when sequencing throughput is fixed.
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Li et al. (Fri,) studied this question.
www.synapsesocial.com/papers/69d8d25f183921ebcaae3c77 — DOI: https://doi.org/10.1093/bioinformatics/btp692
Bo Li
Victor Ruotti
Ron Stewart
Bioinformatics
University of Wisconsin–Madison
Morgridge Institute for Research
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