topr-package | topr |
annotate_with_nearest_gene | Get the nearest gene for one or more snps |
CD_FINNGEN | Finngen r7 Crohnâs disease (K11_CROHNS) |
CD_UKBB | UKBB Crohns disease (ICD 10 code K50) |
create_snpset | Create a dataframe that can be used as input for making effect plots |
create_snpset_code | Show the code/functions used to create a snpset |
effectplot | Create a plot comparing variant effects in two datasets |
effect_plot | Create a plot comparing effects within two datasets |
flip_to_positive_allele_for_dat1 | Flip to the positive allele for dataset 1 |
get_best_snp_per_MB | Get the index/lead variants |
get_gene | Get the genetic position of a gene by gene name |
get_genes_by_Gene_Symbol | Get the genetic position of a gene by its gene name |
get_genes_in_region | Get SNPs/variants within region |
get_gene_coords | Get the genetic position of a gene by gene name |
get_lead_snps | Get the index/lead variants |
get_overlapping_snps_by_pos | Get variants that overlap between two datasets |
get_sign_and_sugg_loci | Get the index/lead variants |
get_snpset | Create a dataframe that can be used as input for making effect plots |
get_snpset_code | Show the code/functions used to get a snpset |
get_snps_within_region | Get SNPs/variants within region |
get_topr_colors | Get the top hit from the dataframe |
get_top_snp | Get the top hit from the dataframe |
locuszoom | Create a locuszoom-like plot |
manhattan | Create a Manhattan plot |
manhattanExtra | Create a Manhattan plot highlighting genome-wide significant and suggestive loci |
match_alleles | Match the variants in the snpset by their alleles |
match_by_alleles | Match the variants in the snpset by their alleles |
match_by_pos | Get variants that overlap between two datasets |
qqtopr | Create a quantile quantile (QQ) plot |
R2_CD_UKBB | Example dataset including the R2 column for the locuszoom plot function |
regionplot | Create a regionplot |
topr | topr |
UC_UKBB | UKBB Ulcerative colitis (ICD 10 code K51) |