create_data_singlecells {alphabetr}  R Documentation 
create_data_singlecells()
simulates a singlecell sequencing
experiment by sampling clones from a clonal structure specified by the user
and using the same error models and frequency distributions used in
create_data
. These functions are almost identical except this
one simulates the sampling and sequencing of single T cells.
create_data_singlecells(TCR, plates = 5, error_drop = c(0.15, 0.01), error_seq = c(0.05, 0.01), error_mode = c("constant", "constant"), skewed = 15, prop_top = 0.5, dist = "linear")
TCR 
The specified clonal structure, which can be created from

plates 
The number of plates of data. The number of singlecells is 96
times 
error_drop 
A vector of length 2 with the mean of the drop error rate and the sd of the drop error rate. 
error_seq 
A vector of length 2 with the mean of the inframe error rate and the sd of the inframe error rate. 
error_mode 
A vector of two strings determining the "mode" of the error
models. The first element sets the mode of the drop errors, and the second
element sets the mode of the inframe errors. The two modes available are
"constant" for a constant error rate and "lognormal" for error rates
drawn from a lognormal distribution. If the mode is set to "constant" the
sd specified in 
skewed 
Number of clones represent the top proportion of the population
by frequency (which is specified by 
prop_top 
The proportion of the population in frequency represented by
the number of clones specified by 
dist 
The distribution of frequency of the top clones. Currently only "linear" is available. 
A list of length 3. The first element is a matrix representing the data of the alpha chains ($alpha), and the second element is a matrix representing the data of beta chains ($beta). The matrix represents the sequencing data by representing the wells of the data by rows and the chain indices by column. Entry [i, j] of the matrix represents if chain j is found in well i (yes == 1, no == 0). e.g. if alpha chain 25 is found in well 10, then [10, 25] of the alpha matrix will be 1.
The third element of the list ($drop) is a matrix that records the index of the clone sampled in the well (col 1), records if a drop error occurred (col 2), and record if an inframe error occurred (col 3).
# see the help for create_clones() for details of this function call clones < create_clones(numb_beta = 1000, dual_alpha = .3, dual_beta = .06, alpha_sharing = c(0.80, 0.15, 0.05), beta_sharing = c(0.75, 0.20, 0.05)) # creating a data set with 480 single cells, lognormal error rates, 10 clones # making up the top 60% of the population in frequency, and a constant # sampling strategy of 50 cells per well for 480 wells (five 96well plates) dat < create_data_singlecells(clones$TCR, plate = 5, error_drop = c(.15, .01), error_seq = c(.05, .001), error_mode = c("lognormal", "lognormal"), skewed = 10, prop_top = 0.6, dist = "linear")