Welcome to the alphabetr vignette! We’ve spent a lot of time trying to develop a TCR sequencing approach that is more scaleable than single-cell sequencing, and we’re excited for others to use it. Our hope is that this vignette will be clear and transparent in showing how we thought to solve this problem, not as be-all panacea for our sequencing woes but as one step towards the field closer to a gold standard. The main purpose of this vignette is to demonstrate how to read in your own data, obtain the results of our paper1, and how to do simulations of your own.
T cell receptors (TCR) are heterodimers of two chains, an alpha chain and a beta chain. Identifying TCRs of T cell clones at a minimum requires the identification of the pair of CDR3 sequences of the alpha and beta chains.
We’ll start by looking at an overview of how to run the alphabetr functions on the sequencing data and then look at the parameters used to simulate the sequencing data.
Sequencing data obtained with the alphabetr approach can be imported using the read_alphabetr() function (see below).
Our goals are to:
Determining candidate pairs. We input the sequencing data into bagpipe(), which determines candidate alpha-beta pairs. The output of bagpipe() are pairs consisting of only one alpha and one beta.
Discriminating dual-alpha and beta-sharing clones. We then utilize freq_estimate()and then use its output frequency estimates in the dual_top()/dual_tail() functions. Although it seems backwards to estimate clonal frequencies before determining dual alpha clones, dual_top()/dual_tail() need these frequencies to determine the dual clones2 dual_top()/dual_tail() will then tell us which candidates that share the same beta are actually one clone express both alpha chains.
Estimating clonal frequencies. The final list of candidate clones, which includes both single-alpha and dual-alpha clones, is then passed into freq_estimate() in order to get a final list of frequeny estimates and 95% frequency confidence intervals. The package includes some helper functions to amend the original list of candidate pairs with the newly determined dual-alpha clones.
The package is currently not on CRAN and must be installed from github. The easiet way to do this is through the devtools package. If you don’t have devtools installed, run the following
install.packages("devtools")With devtools installed, install alphabetr by running
devtools::install_github("edwardslee/alphabetr")And then load the package by running
library(alphabetr)If and when the package is uploaded to CRAN, the package can be simply installed by running
install.packages("alphabetr")alphabetrThe package includes the function read_alphabetr() that will up convert sequencing data to the format used by alphabetr. read_alphabetr() will accept two forms of CSV files:
chain: indentification of "TCRA"/"TCRB" or "alpha"/"beta"well: well number that the chain derives fromcdr3: the CDR3 sequencewell: well number that the chain derives fromcdr3: the CDR3 sequenceThe following is a csv file in the 3-column form
# using a string to be read as a csv file (ignore this and see next line of code)
strcsv <-'"chain","well","cdr3"\n"alpha","1","CAVTGGDKLIF"\n"alpha","1","CALDGDKIIF"\n"alpha","2","CAVTGGDKLIF"\n"beta","1","CASGLARAEQYF"\n"beta","2","CASSEGDKVIF"\n"beta","2","CSEVHTARTQYF"'
con <- textConnection(strcsv)
csv3 <- read.csv(con)
# looking at the csv file
head(csv3)
#> chain well cdr3
#> 1 alpha 1 CAVTGGDKLIF
#> 2 alpha 1 CALDGDKIIF
#> 3 alpha 2 CAVTGGDKLIF
#> 4 beta 1 CASGLARAEQYF
#> 5 beta 2 CASSEGDKVIF
#> 6 beta 2 CSEVHTARTQYFAnd the following is the same data in two 2-column csv files:
# TCRA file
strcsv <-'"well","cdr3"\n"1","CAVTGGDKLIF"\n"1","CALDGDKIIF"\n"2","CAVTGGDKLIF"'
con_alpha <- textConnection(strcsv)
csv2_alpha <- read.csv(con_alpha)
# TCRB file
strcsv <-'"well","cdr3"\n"1","CASGLARAEQYF"\n"2","CASSEGDKVIF"\n"2","CSEVHTARTQYF"'
con_beta <- textConnection(strcsv)
csv2_beta <- read.csv(con_beta)
head(csv2_alpha)
#> well cdr3
#> 1 1 CAVTGGDKLIF
#> 2 1 CALDGDKIIF
#> 3 2 CAVTGGDKLIF
head(csv2_beta)
#> well cdr3
#> 1 1 CASGLARAEQYF
#> 2 2 CASSEGDKVIF
#> 3 2 CSEVHTARTQYFTo load your csv files, the call of read_alphabetr() differs depending on the format of your csv file(s)
# if using one 3 column csv file, using the data argument
dat <- read_alphabetr(data = "alphabetr_data.csv")
# if using two 2 col csv files, use the data_alpha and data_beta arguments
dat <- read_alphabetr(data_alpha = "alphabetr_data_alpha.csv"
data_beta = "alphabetr_data_beta.csv")Just to demonstrate with the dummy csv file we created just before:
# using a string to be read as a csv file (ignore this and see next line of code)
strcsv <-'"chain","well","cdr3"\n"alpha","1","CAVTGGDKLIF"\n"alpha","1","CALDGDKIIF"\n"alpha","2","CAVTGGDKLIF"\n"beta","1","CASGLARAEQYF"\n"beta","2","CASSEGDKVIF"\n"beta","2","CSEVHTARTQYF"'
con <- textConnection(strcsv)
# importing the csv file into the format that alphabetr will use
dat <- read_alphabetr(data = con)
dat
#> $alpha
#> [,1] [,2]
#> [1,] 1 1
#> [2,] 1 0
#>
#> $beta
#> [,1] [,2] [,3]
#> [1,] 1 0 0
#> [2,] 0 1 1
#>
#> $alpha_lib
#> [1] "CAVTGGDKLIF" "CALDGDKIIF"
#>
#> $beta_lib
#> [1] "CASGLARAEQYF" "CASSEGDKVIF" "CSEVHTARTQYF"The output of read_alphabetr() is a list of length four. The alpha component contains the binary matrix that represents which alpha chains (indexed by column) are found in which wells (indexed by row). The beta component is the analogous binary matrix for beta chains. The alpha_lib and beta_lib are vectors that indicate the actual CDR3 sequences for each chain. For example,
# the cdr3 sequence of alpha_2
dat$alpha_lib[2]
#> [1] "CALDGDKIIF"
# the cdr3 sequence of beta_3
dat$beta_lib[3]
#> [1] "CSEVHTARTQYF"The rest of the vignette will discuss how to perform simulations on synthetic data sets (by using the function create_clones() and create_data()). The output of create_data() is the same way as the output of read_alphabetr() would be used, and so although the rest of the vignette is about performing simulations, the same exact can be used on real data that is processed by read_alphabetr().
Simulating the experimental data involves choosing parameters for two domains:
Clonal structure. We create a T cell population using the function create_clones(), which is fully described below, so all I want to do is illustrate what degree of sharing means. Suppose we have the clones with the following chains: a1b2, a2b1, a2b3, a3a4b4. We have four unique alpha chains (a1, a2, a3, a4), one of which is shared by two clones (a2 is shared by a2b1, a2b3). In this population, 25% of the alpha chains are shared by two clones, and 75% of the alpha chains are not shared.
Simulating the sequencing experiment. Just a remark that there’s a lot of parameters to simulate on the experimental side of things.
This section of the vignette will show you how to run simulations from start to finish in order to obtain the type of results as shown in the paper. We will first create T cell populations with user-specified attributes, use functions in alphabetr to figure our candidates pairs, discriminate between dual-alpha and beta-sharing clones, and then determine clonal frequencies.
create_clones() will create a T cell population with a structure specified by you. The attributes that can be changed are
In order to create a population containing
We run the following
set.seed(290) # to make the results reproducible
clonal <- create_clones(numb_beta = 1000,
dual_beta = 0.05,
dual_alpha = .3,
alpha_sharing = c(0.80, 0.15, 0.05),
beta_sharing = c(0.75, 0.20, 0.05))The function arguments are fairly straightforward: numb_beta is the number of unique beta chains in the population, dual is the proportion of clones with dual alpha chains, and alpha_sharing and beta_sharing are the vectors that represent the degree of sharing. Position i of the sharing vectors represent the proportion of the chains shared by i clones.
The output is a list containing different useful versions of the clonal structure
# Clones ordered by beta index
ordered_clones <- clonal$ordered
# Clones randomly ordered in order to assign random clonal frequencies later
random_clones <- clonal$TCR
# Clones that express two different alpha chains and two different beta chains
dual_alpha <- clonal$dual_alpha
dual_beta <- clonal$dual_betaEach of these are 3 column matrices, where each row represents a clone, the first column is the beta chain index, and the second and third columns are the alpha indices. If the clone expresses only one alpha chain, then the 2nd and 3rd columns will be equal. For example,
# single TCR clones
random_clones[5:7, ]
#> beta1 beta2 alpha1 alpha2
#> [1,] 383 383 519 519
#> [2,] 753 753 1031 1031
#> [3,] 353 353 1121 1121
# dual TCR-alpha clones
random_clones[49:50, ]
#> beta1 beta2 alpha1 alpha2
#> [1,] 477 477 372 116
#> [2,] 645 645 851 123
# dual TCR-beta clones
random_clones[47:48, ]
#> beta1 beta2 alpha1 alpha2
#> [1,] 821 318 287 287
#> [2,] 408 170 638 638For the paper, the clonal structures were created with the following code
# Sharing vectors; with this, 1692 beta chains results in 2100 unique clones
share_alph <- c(.816, .085, .021, .007, .033, .005, .033)
share_beta <- c(.859, .076, .037, .019, .009)
# Creating a population of 2100 clones with specified sharing and
# 30% dual-alpha clones and 6% dual-beta clones
set.seed(258) # reproducibility for the vignette
TCR_pairings <- create_clones(numb_beta = 1787,
dual_beta = 0.06,
dual_alpha = 0.3,
alpha_sharing = share_alph,
beta_sharing = share_beta)
TCR_clones <- TCR_pairings$TCRWe’ll use TCR_clones, which contains the clones in random order, in the next section to simulate sequencing data.
Now that we’ve created the clones with their alpha and beta sequences (with each unique chain represented by an integer/index), we can simulate sequencing data. We do this by using the function create_data(). create_data() will sample the clones from a skewed distribution into the wells of 96-well plates, which is what would happen in a sequencing experiment by staining T cells with tetramer and using a sorter to sample them into plates.
A number of experimental parameters can be changed to simulate different experimental settings. These parameters and their corresponding arguments in create_data() are
plates: the number of 96-well plates used in the experimenterror_drop: a vector that contains the mean error “drop-out” rate and the standard deviation of the error rate (if using a lognormal error model). The drop rate is the probability that the chains of a clone can fail to be sequenced (and thus not appear in our final data set)error_mode determines whether the error rates are constant or drawn from a lognormal distributionerror_droperror_seq: a vector that contains the mean “in-frame” sequencing error rate and the standard deviation of the error rate if using a lognormal error model. This is the probability that a given chain will be sequenced incorrectly and produce an incorrect “false” sequence (which cannot distinguished from “true” sequences).error_drop, this argument is a vector of length 2 where the first element is the mean and the second element is the standard deviationerror_mode determines whether the error rates are constant or drawn from a lognormal distributionerror_droperror_mode: a vector that specifies the error model of the drop errors and the in-frame errors"constant" for a constant error model or "lognormal" for error rates drawn from a lognormal distributionskewed: the number of clones that represent the “top proportion” of the population in frequency; this top “proportion” is specified in the pct_top argumentprop_top: the proportion of the population by frequency that is represented by the top clones (of which there are skewed number of them)dist: to developed in the future, but this option controls the shape of the frequency distribution; always set to "linear" for nownumb_cells: sampling strategy that keeps track of the sample sizes of the wells; more details belowcreate_data() takes a matrix of clones as an input, such as TCR_clones, and the order the clones appear in this matrix determines their relative frequencies. The first skewed number of rows of the input matrix is used as the clones representing the top proportion of the population, and create_data() internally distributes them in a descending, linear way across the top. The other clones of the tail then have the same frequency, all adding up to the tail proportion of the population.
To illustrate this better, if we were to pass skewed = 25 and prop_top = 0.6 into create_data(), then the clones represented by the first 25 rows of TCR_clones make up the top 60% of the population, and the other 2075 clones make the other 40% of the population.
The numb_cells argument is a 2 column matrix, where for each row, the 1st column represents the sample size in the well, and the 2nd column is the number of wells with that sample size. You must ensure that the number of wells specified by numb_cells is equal to 96 * number_plates.
# 5 plates (= 480 wells), every well has a sample size of 50 cells
numb_cells <- matrix(c(50, 480), ncol = 2)
# 1 plate (= 96 wells), 48 wells with 100 cells/well, 48 wells with 200 cells/well
numb_cells <- matrix(c(100, 200, 48, 48), ncol = 2)Here are the parameters used in the paper with the “high-mixed” sampling strategy:
# Different experimental parameters
number_plates <- 5 # five 96-well plates
err_drop <- c(0.15, .01) # drop error rate distribution ~ lognormal(.15, .1)
err_seq <- c(0.02, .005) # in frame error rate dist ~ lognormal(.02, .005)
err_mode <- c("constant", "constant") # lognormal error distributions
number_skewed <- 25 # 25 clones representing the top proportion of population
pct_top <- 0.5 # top of population represents 50% of population
dis_behavior <- "linear" # only option avaiable is linear at the moment
# Mixed sampling strategy: 128 wells of 20 cells/well, 64 wells of 50 cells/well,
# 96 wells of 100 cells/well, 200 cells/well, 300 cells/well each
numb_cells <- matrix(c(20, 50, 100, 200, 300,
128, 64, 96, 96, 96), ncol = 2)
# Creating the data sets
data_tcr <- create_data(TCR = TCR_clones,
plates = number_plates,
error_drop = err_drop,
error_seq = err_seq,
error_mode = err_mode,
skewed = number_skewed,
prop_top = pct_top,
dist = dis_behavior,
numb_cells = numb_cells)
# Saving the data for alpha chains and data for beta chains
data_alph <- data_tcr$alpha
data_beta <- data_tcr$betaThe output of create_data() is a list, and the alpha and beta components contain the data for alpha chains and beta chains respectively. Each is a matrix where the rows represent the columns represent the chain indices and the row represents the well. If a well contains a chain, then the row representing that well has a 1 in the chain’s column and 0 if the well does not contain that chain (e.g. if well #25 contains beta 20, then data_beta[25, 20] is 1).
Now that we’ve created the data set, we can begin to apply the algorithms to determine TCRs. The default parameters should work sufficiently well for most data sets
# Normally you would want to set rep = 100 or more
pairs <- bagpipe(alpha = data_alph, beta = data_beta, rep = 5)The output of bagpipe is a matrix with the candidate pairs and the proportion of replicates that each candidate pair appears in.
head(pairs)
#> beta1 beta2 alpha1 alpha2 prop_replicates
#> [1,] 1 1 272 272 1.0
#> [2,] 3 3 935 935 1.0
#> [3,] 4 4 351 351 0.2
#> [4,] 4 4 935 935 0.6
#> [5,] 4 4 1118 1118 0.2
#> [6,] 5 5 714 714 1.0You can clearly see that all of the candidate pairs are single TCR clones at this point. We will attempt to determine dual TCR clones later on in the vignette.
Before moving on, you may choose to the filter the candidate pairs with a threshold of the proportion of replicates that a candidate pair must appear in. Increasing the threshold will significantly decrease the false pairing rate (i.e. the rate at which incorrect pairs are identified) while sacrificing depth of the tail and depth of dual TCR-alpha clone identification.
Our own simulations seem to indicate that a threshold of 0.3 to 0.5 gives a good balance of false pairing rate, tail depth, and dual depth:
# remove candidate pairs that don't appear in more than 30% of replicates
pairs <- pairs[pairs[, "prop_replicates"] > .3, ]
head(pairs)
#> beta1 beta2 alpha1 alpha2 prop_replicates
#> [1,] 1 1 272 272 1.0
#> [2,] 3 3 935 935 1.0
#> [3,] 4 4 935 935 0.6
#> [4,] 5 5 714 714 1.0
#> [5,] 6 6 1045 1045 1.0
#> [6,] 7 7 258 258 1.0With the candidate alpha/beta pairs, we perform an initial frequency estimation as though each candidate pair represents a distinct clone. This is an immediately incorrect assumption because at this point: dual-alpha clones are represented as two distinct clones that share the same beta chain (e.g. if \(\beta_1, \alpha_1, \alpha_2\) is a dual clone, then we will have two candidate pairs \(\beta_1, \alpha_1\) and \(\beta_1, \alpha_2\) at this point). We use the estimated frequencies in order to discriminate between beta-sharing clones and dual-alpha clones.
In order to perform frequency estimation, we use freq_estimate(). The arguments alpha and beta require the sequencing data sets about alpha and beta chains respectively; pair takes the output of bagpipe; error is the experimental error dropout rate; and cells is the sample sizes of the wells and the number of wells with those sample sizes (in the same format as numb_cells in bagpipe()).
Using the data and output of bagipe() from above, we perform frequency estimation:
freq_init <- freq_estimate(alpha = data_alph,
beta = data_beta,
pair = pairs,
error = 0.15,
numb_cells = numb_cells)
head(freq_init)
#> beta1 beta2 alpha1 alpha2 MLE CI_up CI_low
#> 1 1 1 272 272 0.0003040555 0.0005074374 0.0001747017
#> 2 3 3 935 935 0.0002265519 0.0003916560 0.0001105269
#> 3 4 4 935 935 0.0003258786 0.0005390270 0.0001923780
#> 4 5 5 714 714 0.0003066693 0.0005094431 0.0001754589
#> 5 6 6 1045 1045 0.0003258786 0.0005380399 0.0001920682
#> 6 7 7 258 258 0.0003079321 0.0004802097 0.0001577869
#> CI_length pct_replicates
#> 1 0.0003327357 1.0
#> 2 0.0002811291 1.0
#> 3 0.0003466491 0.6
#> 4 0.0003339843 1.0
#> 5 0.0003459717 1.0
#> 6 0.0003224229 1.0You can see that the output shows you the alpha and beta indices of the clone, the frequency point estimate (under MLE), the upper and lower limits of the 95% confidence interval (CI_up and CI_low respectively), the length of the confidence interval, and the number of replicates each clone was found in during bagpipe().
In order to disciminate between beta-sharing and dual-alpha clones, we needed the frequency estimation of the candidate pairs given by bagpipe(), and the estimated frequencies are used to parse between these situations. Two different functions are needed for this: dual_top() is used to usually determine dual-alpha TCRs in more common clones, and dual_tail() is used to determine dual TCR-alpha TCRs in rare clones in the tail.
# determining duals in the top; note the use of the error rate
common_dual <- dual_top(alpha = data_alph,
beta = data_beta,
pair = freq_init,
error = err,
numb_cells = numb_cells)
# determining duals in the tail; note that this does NOT use the error rate
tail_dual <- dual_tail(alpha = data_alph,
beta = data_beta,
freq_results = freq_init,
numb_cells = numb_cells)The arguments of these functions are the same arguments used before.
We combine the output of both functions to obtain a data frame with all of the dual clones:
clones_dual <- rbind(common_dual, tail_dual)
head(clones_dual)
#> beta1 beta2 alpha1 alpha2
#> 1 258 258 1643 892
#> 2 570 570 373 141
#> 3 616 616 1280 648
#> 4 740 740 373 1280
#> 5 835 835 550 1359
#> 6 1205 1205 33 335Now that we identified dual TCR-alpha clones, all that’s left is to estimate their frequencies and replace the corresponding beta-sharing candidate pairs with the dual TCR-alpha clone:
# Find the frequencies of the newly identified dual clones
freq_dual <- freq_estimate(alpha = data_alph,
beta = data_beta,
pair = clones_dual,
error = 0.15,
numb_cells = numb_cells)
# Remove the candidate beta-sharing clones and replace with the dual clones
tcrpairs <- combine_freq_results(freq_init, freq_dual)combine_freq_results() is a helper function that will combine the initial frequency results and the freshly calculated dual frequency results. It will find the two rows containing the candidate pairs that derived from the dual clone and replace it with the results of the dual clone. The first argument is the initial frequency results, and the second argument is the dual frequency results.
The final results of processing our TCR sequencing data is contained in our data frame tcrpairs
head(tcrpairs)
#> beta1 beta2 alpha1 alpha2 MLE CI_up CI_low CI_length
#> 1 1637 1637 373 1032 0.04271497 0.04651125 0.03201378 0.01449746
#> 2 258 258 1643 892 0.04146939 0.04507328 0.03123586 0.01383743
#> 3 801 801 1643 1643 0.04083954 0.04767091 0.03491152 0.01275939
#> 4 616 616 1280 648 0.04002182 0.04353211 0.02995146 0.01358065
#> 5 917 917 373 373 0.03696094 0.04328901 0.03151756 0.01177145
#> 6 605 605 157 157 0.03674642 0.04295367 0.03138863 0.01156504
#> pct_replicates
#> 1 -1.0
#> 2 -1.0
#> 3 1.0
#> 4 -1.0
#> 5 0.6
#> 6 1.0Note that if a clone is dual, then the pct_replicates column is set to -1.
Two functions are included in the package to evaluate the performance of the frequency estimation and the dual discrimination. The function dual_eval() is used to determine how well the dual discrimination went.
dual_res <- dual_eval(duals = clones_dual,
pair = freq_init,
TCR = TCR_pairings$TCR,
number_skewed = number_skewed,
TCR_dual = TCR_pairings$dual_alpha)
# listing the false dual rate and the adjusted dual depths of the top and tail clones
dual_res$fdr
#> [1] 0.1933333
dual_res$adj_depth_top
#> [1] 1
dual_res$adj_depth_tail
#> [1] 0.9586777The function freq_eval() is used to determine how precise the frequency estimates are and how many 95% confidence intervals contain the true clonal frequency.
freq_res <- freq_eval(freq = tcrpairs,
number_skewed = number_skewed,
TCR = TCR_pairings$TCR,
numb_clones = nrow(TCR_pairings$TCR),
prop_top = pct_top)
# CV of estimates and the proportion of CIs with correct frequency
freq_res$cv
#> [1] 0.08703727
freq_res$correct
#> [1] 0.8333333http://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1005313↩
the paper explains why this is done↩