gwas_format | R Documentation |
Format GWAS summary statistics for CAUSE
gwas_format(
X,
snp,
beta_hat,
se,
A1,
A2,
chrom,
pos,
p_value,
sample_size,
allele_freq,
output_file,
compute_pval = TRUE
)
X |
data.frame |
snp |
Column name containing SNP ID |
beta_hat |
Column name containing effect estimate |
se |
Column name containing standard error of beta_hat |
A1 |
Column name containing effect allele |
A2 |
Column name containing other allele |
chrom |
Chromosome column (optional) |
pos |
Position column (optional) |
p_value |
p-value column (optional) |
sample_size |
Sample size column (optional) or an integer |
output_file |
File to write out formatted data. If missing formatted data will be returned. |
compute_pval |
Logical, compute the p-value using a normal approximation if missing? Defaults to TRUE. |
This function will try to merge data sets X1 and X2 on the specified columns. Where necessary, it will flip the sign of effects so that the effect allele is the same in both data sets. It will remove variants with ambiguous alleles or where the alleles (G/C or A/T) or with alleles that do not match between data sets (e.g A/G in one data set and A/C in the other). It will not remove variants that are simply strand flipped between the two data sets (e. g. A/C in one data set, T/G in the other).
A data frame with columns chrom, pos, snp, A1, A2, beta_hat, se, p_value, and sample_size with all SNPs aligned so that A is the effect allele. This is ready to be used with gwas_merge with formatted = TRUE.
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