| multifinemap | R Documentation | 
Handle fine-mapping across multiple tools.
multifinemap(
  dat,
  locus_dir,
  fullSS_path = NULL,
  finemap_methods = c("ABF", "SUSIE", "FINEMAP"),
  finemap_args = NULL,
  dataset_type = "GWAS",
  force_new_finemap = FALSE,
  LD_reference = NULL,
  LD_matrix = NULL,
  n_causal = 5,
  compute_n = "ldsc",
  standardise_headers = FALSE,
  conditioned_snps = NULL,
  credset_thresh = 0.95,
  consensus_thresh = 2,
  case_control = TRUE,
  priors_col = NULL,
  conda_env = "echoR_mini",
  nThread = 1,
  seed = 2022,
  verbose = TRUE
)
dat | 
 Fine-mapping results data.  | 
locus_dir | 
 Locus-specific directory to store results in.  | 
fullSS_path | 
 Path to the full summary statistics file (GWAS or QTL) that you want to fine-map. It is usually best to provide the absolute path rather than the relative path.  | 
finemap_methods | 
 Fine-mapping methods to run. See lfm for a list of all fine-mapping methods currently available.  | 
finemap_args | 
 A named nested list containing additional arguments 
for each fine-mapping method. e.g.
  | 
dataset_type | 
 The kind dataset you're fine-mapping (e.g. GWAS, eQTL, tQTL). This will also be used when creating the subdirectory where your results will be stored (e.g. Data/<dataset_type>/Kunkle_2019).  | 
force_new_finemap | 
 By default, if an fine-mapping results file for
a given locus is already present,
then echolocatoR will just use the preexisting file.
Set   | 
LD_reference | 
 Name of the LD reference panel.  | 
LD_matrix | 
 Linkage Disequilibrium (LD) matrix to use for fine-mapping.  | 
n_causal | 
 The maximum number of potential causal SNPs per locus. This parameter is used somewhat differently by different fine-mapping tools. See tool-specific functions for details.  | 
compute_n | 
 How to compute per-SNP sample size (new column "N"). 
  | 
standardise_headers | 
 Standardise headers first.  | 
conditioned_snps | 
 Which SNPs to conditions on when fine-mapping with (e.g. COJO).  | 
credset_thresh | 
 The minimum mean Posterior Probability (across all fine-mapping methods used) of SNPs to be included in the "mean.CS" column.  | 
consensus_thresh | 
 The minimum number of fine-mapping tools in which a SNP is in the Credible Set in order to be included in the "Consensus_SNP" column.  | 
case_control | 
 Whether the summary statistics come from a case-control
study (e.g. a GWAS of having Alzheimer's Disease or not) (  | 
priors_col | 
 [Optional] Name of the a column in 
  | 
conda_env | 
 Conda environment to use.  | 
nThread | 
 Number of threads to parallelise across (when applicable).  | 
seed | 
 Set the random seed for reproducible results.  | 
verbose | 
 Print messages.  | 
Other finemapping functions: 
create_method_path(),
multifinemap_handler_method(),
multifinemap_handler()
dat <- echofinemap::drop_finemap_cols(dat = echodata::BST1)
LD_matrix <- echodata::BST1_LD_matrix
locus_dir <- file.path(tempdir(),echodata::locus_dir) 
dat2 <- echofinemap::multifinemap(dat = dat, 
                                 locus_dir = locus_dir,
                                 LD_matrix = LD_matrix)
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