View source: R/check_bp_range.R
check_bp_range | R Documentation |
Ensure that the Base-pair column values are all within the range for the chromosome
check_bp_range(
sumstats_dt,
path,
ref_genome,
log_folder_ind,
imputation_ind,
check_save_out,
tabix_index,
nThread,
log_files
)
path |
Filepath for the summary statistics file to be formatted. A dataframe or datatable of the summary statistics file can also be passed directly to MungeSumstats using the path parameter. |
ref_genome |
name of the reference genome used for the GWAS ("GRCh37" or "GRCh38"). Argument is case-insensitive. Default is NULL which infers the reference genome from the data. |
log_folder_ind |
Binary Should log files be stored containing all filtered out SNPs (separate file per filter). The data is outputted in the same format specified for the resulting sumstats file. The only exception to this rule is if output is vcf, then log file saved as .tsv.gz. Default is FALSE. |
imputation_ind |
Binary Should a column be added for each imputation step to show what SNPs have imputed values for differing fields. This includes a field denoting SNP allele flipping (flipped). On the flipped value, this denoted whether the alelles where switched based on MungeSumstats initial choice of A1, A2 from the input column headers and thus may not align with what the creator intended.Note these columns will be in the formatted summary statistics returned. Default is FALSE. |
tabix_index |
Index the formatted summary statistics with tabix for fast querying. |
nThread |
Number of threads to use for parallel processes. |
log_files |
list of log file locations |
list containing sumstats_dt, the modified summary statistics data table object and the log file list
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