dat_to_gwasvcf | R Documentation |
Function to convert a data.frame to gwasvcf format.
dat_to_gwasvcf( dat, out, chr_col, pos_col, nea_col, ea_col, snp_col = NULL, eaf_col = NULL, beta_col = NULL, se_col = NULL, pval_col = NULL, n = NULL, n_case = NULL, name = NULL, bcf_tools = NULL, verbose = TRUE )
dat |
Data.frame |
out |
Path to save output |
chr_col |
Column name for chromosome |
pos_col |
Column name for position |
nea_col |
Column name for non-effect allele |
ea_col |
Column name for effect allele |
snp_col |
Column name for SNP (Optional) |
eaf_col |
Column name for effect allele frequency (Optional) |
beta_col |
Column name for beta (Optional) |
se_col |
Column name for standard error (Optional) |
pval_col |
Column name for P value (Optional) NB: P values will be saved as 10^-P |
n |
Sample size (Optional), can be int or column name |
n_case |
Number of cases (Optional), can be int or column name |
name |
Trait name (Optional), can be string or column name |
bcf_tools |
Path to bcf_tools (Optional) |
verbose |
Display verbose information (Optional, boolean) |
gwasvcf object
[file_to_gwasvcf()] for converting files.
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