cloneTrack | R Documentation |
Creates line plot tracking amino acid frequencies across multiple samples
cloneTrack( study_table, sample_list = NULL, sequence_track = NULL, unassigned = TRUE )
study_table |
A tibble of productive amino acid sequences generated by LymphoSeq function productiveSeq where the aggregate parameter was set to "junction_aa" |
sample_list |
A character vector of one or more repertoire_ids to track. If set to NULL (default), all repertoire_ids in the sequence matrix will be tracked. |
sequence_track |
An optional character vector of one or more amino acid sequences to track. If set to NULL (default), will pull all junction_aa sequences from the sequence matrix. |
unassigned |
The plot is made using the package ggplot2 and can be reformatted using ggplot2 functions. See examples below.
Returns a line plot showing the amino acid frequencies across multiple samples in the sequence matrix where each line represents one unique sequence.
An excellent resource for examples on how to reformat a ggplot can be found in the R Graphics Cookbook online (http://www.cookbook-r.com/Graphs/).
file_path <- system.file("extdata", "TCRB_sequencing", package = "LymphoSeq2") stable <- readImmunoSeq(path = file_path) atable <- productiveSeq(study_table = stable, aggregate = "junction_aa") top_freq <- topFreq(atable, frequency = 0.001) # Track clones without mapping or tracking specific sequences cloneTrack(atable) # Track top 20 clones mapping to the CD4 and CD8 samples cloneTrack(atable, sample_list = c("TRB_CD4_949", "TRB_CD8_949"), sequence_track = top_freq$junction_aa[1:20], unassigned = TRUE) # Track the top 10 clones from top.freq cloneTrack(study_table = atable, sequence_track = top_freq$junction_aa[1:10], unassigned = FALSE) # Track clones mapping to the CD4 and CD8 samples while ignoring all others cloneTrack(study_table = atable, sample_list = c("TRB_CD4_949", "TRB_CD8_949"), unassigned = FALSE) # Track clones mapping to the CD4 and CD8 samples and track 2 specific sequences cloneTrack(study_table = atable, sample_list = c("TRB_CD4_949", "TRB_CD8_949"), sequence_track = c("CASSPPTGERDTQYF", "CASSQDRTGQYGYTF"), unassigned = FALSE)
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