Description Usage Arguments Details Value
mxr_clump
determines the clumps of SNPs based on LD along the region
that registers a significant association signal with the phenotype. This uses
the --clump
command of plink.
https://www.cog-genomics.org/plink2
1 2 3 4 |
emmax2_results |
The fullpath and filename of the results of mxr_associate. |
genotype_prefix |
The fullpath and prefix of the bim/bed/fam plink files. |
snp_field |
The column header for the SNP column in the results file from mxr_associate. (Default: "snp_id") |
clump_field |
The column header for the p-value column in the results file from mxr_associate. (Default: "p") |
clump_p1 |
The maximum p-value of the index variants that define each clump. Index variants need to have values between 0 and this p-value. (Default: 0.00001) |
clump_p2 |
The maximum association p-value of SNPs that belonging to the clump formed by an index variant. (Default: 0.01) |
clump_kb |
The maximum distance of a clumped SNP from its index variant. (Default: 200) |
clump_r2 |
The r-squared value of the clumped SNP with its index variant. (Default: 0.50) |
clump_range_border_kb |
The number of kilobases past the region clump-range region. (Default: 20) |
gene_list |
The list of genes must have the following columns: chromosome, start (bp), end (bp), locus_id. These fields must be tab separated and have an appropriately named column header. The chromosome must be coded to correspond to the plink data. @param out_prefix Path and prefix of the output files. |
verbose |
(Optional) Show verbose output. (DEFAULT=FALSE) |
Before running this function, make sure that the mxr_associate function has already been called and that the results are successfully obtained without warnings (that imply fatal errors) or errors.
TRUE if the PLINK run completed successfully. FALSE, otherwise.
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