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ABSTRACT: Motivation
A sequencing-based genomic assay such as ChIP-seq outputs a real-valued signal for each position in the genome that measures the strength of activity at that position. Most genomic signals lack the property of variance stabilization. That is, a difference between 0 and 100 reads usually has a very different statistical importance from a difference between 1000 and 1100 reads. A statistical model such as a negative binomial distribution can account for this pattern, but learning these models is computationally challenging. Therefore, many applications-including imputation and segmentation and genome annotation (SAGA)-instead use Gaussian models and use a transformation such as log or inverse hyperbolic sine (asinh) to stabilize variance.Results
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SUBMITTER: Bayat F
PROVIDER: S-EPMC8652025 | biostudies-literature | 2021 Dec
REPOSITORIES: biostudies-literature