In vjcitn/biocwk312: Workshop intro for Bioconductor 3.12.
knitr::opts_chunk$set(
collapse = TRUE,
comment = "#>"
)
Computing foundations for disease genetics research
Human genetics - basic principles
The EBI/EMBL GWAS catalog
Rare variants: gnomAD (is this available either as a service or a dataset?)
VariantAnnotation and OpenCRAVAT
Additional resources
- epigenetic marks etc from UKBiobank
- Polygenic Risk Scores
vjcitn/biocwk312 documentation built on Jan. 1, 2021, 12:41 p.m.
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knitr::opts_chunk$set( collapse = TRUE, comment = "#>" )
Computing foundations for disease genetics research
Human genetics - basic principles
The EBI/EMBL GWAS catalog
Rare variants: gnomAD (is this available either as a service or a dataset?)
VariantAnnotation and OpenCRAVAT
Additional resources
- epigenetic marks etc from UKBiobank
- Polygenic Risk Scores
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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