View source: R/snp_track_merged.R
| snp_track_merged | R Documentation | 
Manhattan plot of GWAS/QTL data with various fine-mapping related annotations. Support function for plot_locus.
snp_track_merged(
  dat,
  yvar = "-log10(P)",
  labels_subset = c("Lead", "CS", "UCS", "Consensus"),
  absolute_labels = FALSE,
  label_type = "rsid_only",
  label_leadsnp = TRUE,
  sig_cutoff = 5e-08,
  point_alpha = 0.5,
  show.legend = TRUE,
  xtext = TRUE,
  facet_formula = "Method~.",
  dataset_type = NULL,
  genomic_units = "POS",
  remove_duplicates = FALSE,
  strip.text.y.angle = 0,
  show_plot = FALSE,
  verbose = TRUE
)
dat | 
 Data to query transcripts with.  | 
labels_subset | 
 Include colored shapes and RSID labels to help highlight SNPs belonging to one or more of the following groups: Lead, Credible Set, Consensus.  | 
sig_cutoff | 
 Filters out SNPs to plot based on an (uncorrected) p-value significance cutoff.  | 
point_alpha | 
 Opacity of each data point.  | 
xtext | 
 Include x-axis title and text for each track (not just the lower-most one).  | 
facet_formula | 
 Formula to facet plots by. See facet_grid for details.  | 
dataset_type | 
 Dataset type (e.g. "GWAS" or "eQTL").  | 
genomic_units | 
 Which genomic units to return window limits in.  | 
remove_duplicates | 
 Remove duplicate labels when SNPs are part of >1 
group in   | 
strip.text.y.angle | 
 Angle of the y-axis facet labels.  | 
show_plot | 
 Print plot to screen.  | 
verbose | 
 Print messages.  | 
dat <- echodata::BST1[seq_len(100),]
plt <- snp_track_merged(dat = dat, yvar="PP", show_plot=TRUE)
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