Last updated: 2023-06-19

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Knit directory: m6A_in_disease_genetics/

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Ignored files:
    Ignored:    .ipynb_checkpoints/
    Ignored:    analysis/m6A_switch_to_disease_h2g.nb.html

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Unstaged changes:
    Modified:   analysis/index.Rmd
    Modified:   analysis/m6A_switch_to_disease_h2g.Rmd

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These are the previous versions of the repository in which changes were made to the R Markdown (analysis/index.Rmd) and HTML (docs/index.html) files. If you’ve configured a remote Git repository (see ?wflow_git_remote), click on the hyperlinks in the table below to view the files as they were in that past version.

File Version Author Date Message
Rmd b7a7aa3 Jing Gu 2023-05-09 update
html bc330a2 Jing Gu 2023-04-12 update index page
html 98540ac Jing Gu 2023-04-12 update index page
html 86b31ec Jing Gu 2023-04-12 Build site.
Rmd 0e3b2a9 Jing Gu 2023-04-12 publish the initial files
Rmd c558a6b Jing Gu 2023-03-31 Start workflowr project.

Backgrounds

Genetic variants may act through m6A-switch to cause disease

Test the enrichment for dsRNAs formed by m6A-switch with GWAS variants

m6A informed fine-mapping

Are predicted m6A QTLs enriched for GWAS signals?

Are predicted m6A QTLs enriched for ClinVar variants?