# hyprcoloc

**Repository Path**: sheng0825/hyprcoloc

## Basic Information

- **Project Name**: hyprcoloc
- **Description**: No description available
- **Primary Language**: Unknown
- **License**: Not specified
- **Default Branch**: main
- **Homepage**: None
- **GVP Project**: No

## Statistics

- **Stars**: 0
- **Forks**: 0
- **Created**: 2021-07-26
- **Last Updated**: 2021-07-26

## Categories & Tags

**Categories**: Uncategorized

**Tags**: None

## README

# HyPrColoc
Hypothesis Prioritisation in multi-trait Colocalization (HyPrColoc).

Genome-wide association studies (GWAS) have identified thousands of genomic regions affecting complex diseases. The next challenge is to elucidate the causal genes and mechanisms involved. One approach is to use statistical colocalization to assess shared genetic aetiology across multiple related traits (e.g. molecular traits, metabolic pathways and complex diseases) to identify causal pathways, prioritize causal variants and evaluate pleiotropy.

HyPrColoc is an efficient deterministic Bayesian divisive clustering algorithm using GWAS summary statistics that can detect colocalization across vast numbers of traits simultaneously.

## Functions
* hyprcoloc - identifies clusters of colocalized traits and candidate causal SNPs using the HyPrColoc Bayesian divisive clustering algorithm.

## Installation
1. install.packages("devtools")
2. library(devtools)
3. install_github("cnfoley/hyprcoloc", build_opts = c("--resave-data", "--no-manual"), build_vignettes = TRUE)
4. library(hyprcoloc)
5. browseVignettes("hyprcoloc")

## If issue with installation (owing to c++ compiler)
Try replacing 3 above with previous package version:

3. install_github("jrs95/hyprcoloc", build_opts = c("--no-resave-data", "--no-manual"), build_vignettes = TRUE)

\# Note there is no "prior.c" parameter in this version, instead use "prior.2 = 1 - prior.c". Default settings are matched.

Otherwise, on a Windows machine try updating Rtools: remove the previous version of Rtools (probably located C:\Rtools) and download Rtools40 from CRAN [https://cran.r-project.org/bin/windows/Rtools/]

## Example
\# Regression coefficients and standard errors from ten GWAS studies (Traits 1-5, 6-8 & 9-10 colocalize)  
betas <- hyprcoloc::test.betas  
head(betas)  
ses <- hyprcoloc::test.ses  
head(ses)  
  
\# Trait names and SNP IDs  
traits <- paste0("T", 1:10)  
rsid <- rownames(betas)  

\# Colocalization analysis  
hyprcoloc(betas, ses, trait.names=traits, snp.id=rsid)  

## Citations
* HyPrColoc: Foley CN, Staley JR, et al. A fast and efficient colocalization algorithm for identifying shared genetic risk factors across multiple traits. BioRxiv 2019. doi: https://doi.org/10.1101/592238
* HyPrColoc software: Foley, CN and Staley JR. (2020, November 27). cnfoley/hyprcoloc: First release of software (Version v1.0.0). Zenodo. http://doi.org/10.5281/zenodo.4293559
* LD blocks: Berisa T & Pickrell JK. Approximately independent linkage disequilibrium blocks in human populations. Bioinformatics 2016; 32(2):283-285