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R2CPCT - Toolkit for the analysis of WGS and RNA-Seq data from the CPCT-02 and WIDE study.

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This package contains various R functions which are used to import, process and analyze WGS and (matching) RNA-Seq samples derived from the CPCT/Hartwig Medical Foundation collaboration in context of the CPCT-02, DRUP and WIDE studies.

Installation

The latest development version (which requires R ≥v4.0) can easily be installed from this repository using devtools:

# Install using devtools.
devtools::install_github(repo = "J0bbie/R2CPCT")

# Load library
library(R2CPCT)

Additional annotation of genomic variants with VEP.

Prior to import, files need to be annotated with VEP using the workflow and scripts available in https://github.com/J0bbie/VariantAnnotation_VEP.

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Workflow for processing and analyzing whole genome sequencing (WGS) from the HMF.

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