knitr::opts_chunk$set( collapse = TRUE, comment = "#>", fig.path = "Input-" )
The input dataset for a trait (querytrait) should contain the summary data for SNPs in a genomic region around the query variant (querysnpid) and should have the following fields:
For a Case-control dataset
beta: $\beta$ or effect size
varbeta: variance of $\beta$ or square of the standard error of $\beta$
snp: SNP identifier which maybe rsid or CHR_BP_REF_ALT or CHR_BP
type:'cc'
N: sample size
For a Quantitave dataset
When, beta and varbeta are not available the following
beta: $\beta$ or effect size
varbeta: variance of $\beta$ or square of the standard error of $\beta$
snp: SNP identifier which maybe rsid or CHR_BP_REF_ALT or CHR_BP
type:'quant'
N: sample size
sdY: for a quantitative trait, the population standard deviation of the trait.
Additional fields in case of missing beta/varbeta or sdY
MAF: Minor allele frequency (only required when either beta/varbeta or sdY are unavailable)
pvalues: only required when beta/varbeta are unavailable
s: fraction of samples that are cases (only for a case-control trait when beta/varbeta are unavailable)
library(cophescan)
Explore the data structure of the example dataset available in the cophescan package
data("cophe_multi_trait_data") trait_dat = cophe_multi_trait_data$summ_stat$Trait_1 str(trait_dat)
Additional field for cophe.susie
LD: Linkage Disequilibrium matrix with row and column names being the same as the snp field.
trait_dat$LD = cophe_multi_trait_data$LD str(trait_dat$LD[1:10, 1:10])
It is important to check that there is alignment of alleles for which the beta is reported and those in the LD matrix. This can be verified either using coloc::check_alignment or performing a diagnostic check using the susie package https://stephenslab.github.io/susieR/articles/susierss_diagnostic.html.
Note
?coloc::check_dataset
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