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Chunk #65 — Methods — Singleton clustering analysis — Modelling the relationship between clustering patterns and genomic features

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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.
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In each 1-Mb window, we calculated the average signal for 12 genomic features (H3K27ac, H3K27me3, H3K36me3, H3K4me1, H3K4me3, H3K9ac, H3K9me3, exon density, DNase hypersensitivity, CpG island density, lamin-associated domain density and recombination rate), using the previously described source datasets31. For each mixture component, we then applied the following negative binomial regression model to estimate the effects of each feature on the density of that component in 1-Mb windows:\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\log ({Y}_{a,k,w})={\beta }_{0}+{\beta }_{1}{X}_{1,w}+\mathrm{...}+{\beta }_{12}{X}_{12,w}$$\end{document}log(Ya,k,w)=β0+β1X1,w+...+β12X12,w