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The goal of rTCRBCRr is to process the results from clonotyping tools such as trust, mixcr, and immunoseq to analyze the clonotype repertoire metrics
The package is accepted by the CRAN, you can install the released version of rTCRBCRr from CRAN with:
install.packages("rTCRBCRr")You can also install the development version from GitHub with:
# install.packages("devtools")
devtools::install_github("sciencepeak/rTCRBCRr")library("rTCRBCRr")
library("magrittr")
library("readr")present_tool <- c("trust", "mixcr")[1]
example_data_directory <- system.file(paste("extdata", present_tool, sep = "/"), package = "rTCRBCRr")
input_paths <- dir(example_data_directory, full.names = TRUE)
input_files <- dir(example_data_directory, full.names = FALSE)
input_files
#> [1] "sample_01.tsv.bz2" "sample_02.tsv.bz2" "sample_03.tsv.bz2"
sample_names <- sub(".tsv.*", "", input_files)
sample_names
#> [1] "sample_01" "sample_02" "sample_03"
raw_clonotype_dataframe_list <- lapply(input_paths, readr::read_tsv) %>%
magrittr::set_names(., value = sample_names)
raw_clonotype_dataframe_list
#> $sample_01
#> # A tibble: 5,051 x 10
#> `#count` frequency CDR3nt CDR3aa V D J C cid
#> <dbl> <dbl> <chr> <chr> <chr> <chr> <chr> <chr> <chr>
#> 1 1813 0.0664 TGTCAGAAGTATGGTGGCTC~ CQKYG~ IGKV~ . IGKJ~ IGKC asse~
#> 2 1684 0.0833 TGCGCGAGAGATGCGGGGGG~ CARDA~ IGHV~ IGHD~ IGHJ~ IGHG1 asse~
#> 3 1648 0.0815 TGTGCGAGAGGGGGAGTGGA~ CARGG~ IGHV~ IGHD~ IGHJ~ IGHG1 asse~
#> 4 1505 0.0551 TGTCAACAGCTTAGTTATTA~ CQQLS~ IGKV~ . IGKJ~ IGKC asse~
#> 5 1081 0.0396 TGCATGCAAGGTCTACAAAC~ CMQGL~ IGKV~ . IGKJ~ IGKC asse~
#> 6 895 0.0328 TGTCAACAGAGTTACGGTAC~ CQQSY~ IGKV~ . IGKJ~ IGKC asse~
#> 7 866 0.0429 TGTGCGAGAGCCTCTTATTA~ CARAS~ IGHV~ IGHD~ IGHJ~ IGHG1 asse~
#> 8 811 0.0297 TGCATGCAAGCTCTACAAAC~ CMQAL~ IGKV~ . IGKJ~ IGKC asse~
#> 9 767 0.0281 TGCTGCTCATATACAGGCAG~ CCSYT~ IGLV~ . IGLJ~ IGLC asse~
#> 10 761 0.0377 TGTGCTAGGGCGGCCAGTGG~ CARAA~ IGHV~ IGHD~ IGHJ~ IGHG1 asse~
#> # ... with 5,041 more rows, and 1 more variable: cid_full_length <dbl>
#>
#> $sample_02
#> # A tibble: 5,915 x 10
#> `#count` frequency CDR3nt CDR3aa V D J C cid
#> <dbl> <dbl> <chr> <chr> <chr> <chr> <chr> <chr> <chr>
#> 1 5392 0.0875 TGCATGCAAGCTCTACAAAC~ CMQAL~ IGKV~ . IGKJ~ IGKC asse~
#> 2 4470 0.0725 TGCATGCAATCTCTACAAGC~ CMQSL~ IGKV~ . IGKJ~ IGKC asse~
#> 3 3852 0.0625 TGTCAGCAGTATAATAACTG~ CQQYN~ IGKV~ . IGKJ~ IGKC asse~
#> 4 2893 0.0470 TGCCAACGATATGATACTTA~ CQRYD~ IGKV~ . IGKJ~ IGKC asse~
#> 5 2698 0.0438 TGTCAGCAGTATAATAACTG~ CQQYN~ IGKV~ . IGKJ~ IGKC asse~
#> 6 1691 0.0509 TGTGCGAGACAAGTTCGTCC~ CARQV~ IGHV~ IGHD~ IGHJ~ IGHG1 asse~
#> 7 1589 0.0478 TGTGCGAGACACGCGGATAC~ CARHA~ IGHV~ IGHD~ IGHJ~ IGHG1 asse~
#> 8 1373 0.0414 TGTGCGAGACAGTTTTACTA~ CARQF~ IGHV~ IGHD~ IGHJ~ IGHG1 asse~
#> 9 1319 0.0397 TGTGCGGCAGAGTGGGCTAG~ CAAEW~ IGHV~ IGHD~ IGHJ~ IGHG1 asse~
#> 10 1172 0.0353 TGTGCGAGGGGGGTCAATTA~ CARGV~ IGHV~ IGHD~ IGHJ~ IGHG1 asse~
#> # ... with 5,905 more rows, and 1 more variable: cid_full_length <dbl>
#>
#> $sample_03
#> # A tibble: 6,027 x 10
#> `#count` frequency CDR3nt CDR3aa V D J C cid
#> <dbl> <dbl> <chr> <chr> <chr> <chr> <chr> <chr> <chr>
#> 1 14711 0.335 TGTACACTCCTGGTGACCAC~ CTLLV~ IGHV~ IGHD~ IGHJ~ IGHG1 asse~
#> 2 13909 0.341 TGCCAGTCCTATGACAGCAG~ CQSYD~ IGLV~ . IGLJ~ IGLC asse~
#> 3 6790 0.166 TGCAGCTCACACACAAGCAG~ CSSHT~ IGLV~ . IGLJ~ IGLC asse~
#> 4 4209 0.0959 TGTGCGAGAGCCCTCCCCTA~ CARAL~ IGHV~ IGHD~ IGHJ~ IGHG1 asse~
#> 5 3727 0.0850 TGTGCGAGAGCCCTCCCCTA~ CARAL~ IGHV~ IGHD~ IGHJ~ IGHA1 asse~
#> 6 910 0.0223 TGCAGCTCATATGCAGGCGG~ CSSYA~ IGLV~ . IGLJ~ IGLC asse~
#> 7 771 0.0189 TGTGCAGCATGGGAAGACAG~ CAAWE~ IGLV~ . IGLJ~ IGLC asse~
#> 8 768 0.0175 TGTGCGAGATTTTTCCATGA~ CARFF~ IGHV~ IGHD~ IGHJ~ IGHG3 asse~
#> 9 701 0.0172 TGCCAGTCCTATGACAGCAG~ CQSYD~ IGLV~ . IGLJ~ IGLC asse~
#> 10 628 0.0143 TGTGCGAGAGATGTACTATT~ CARDV~ IGHV~ IGHD~ IGHJ~ IGHG1 asse~
#> # ... with 6,017 more rows, and 1 more variable: cid_full_length <dbl>The tidy-up consists of four steps, namely four functions:
# If you only want to test one sample, you can process the only sample as follows.
the_divergent_clonotype_dataframe <- raw_clonotype_dataframe_list[["sample_01"]] %>%
format_clonotype_to_immunarch_style(., clonotyping_tool = present_tool) %>%
remove_nonproductive_CDR3aa %>%
annotate_chain_name_and_isotype_name %>%
merge_convergent_clonotype
# Then the only one sample should be put into a list, element of which uses the sample name,
# because the later step need a named list of data frames as input.
divergent_clonotype_dataframe_list <- list(sample_01 = the_divergent_clonotype_dataframe)
# Otherwise, normally you will have multiple samples,
# then functional style of processing is preferred as follows.
divergent_clonotype_dataframe_list <- raw_clonotype_dataframe_list %>%
lapply(., format_clonotype_to_immunarch_style, clonotyping_tool = present_tool) %>%
lapply(., remove_nonproductive_CDR3aa) %>%
lapply(., annotate_chain_name_and_isotype_name) %>%
lapply(., merge_convergent_clonotype)This step consists of three functions.
# handle repertoire metrics for all the chains.
all_sample_all_chain_all_metrics_wide_format_dataframe_list <- the_divergent_clonotype_dataframe_list %>%
lapply(., compute_repertoire_metrics_by_chain_name)
all_sample_all_chain_all_metrics_wide_format_dataframe_list
#> $sample_01
#> diversity clonality richness evenness median
#> IGH 5.4161872 0.26283295 1552 0.7371670 0.0001509510
#> IGK 5.2677388 0.28931127 1656 0.7106887 0.0000908224
#> IGL 4.8949171 0.25490053 713 0.7450995 0.0004132231
#> TRA 4.3018929 0.06585582 100 0.9341442 0.0064377682
#> TRB 4.8358496 0.08467479 197 0.9153252 0.0036429872
#> TRD 0.6730117 0.02904941 2 0.9709506 0.5000000000
#> TRG 0.6931472 0.00000000 2 1.0000000 0.5000000000
#>
#> $sample_02
#> diversity clonality richness evenness median
#> IGH 5.3401961 0.28075859 1677 0.7192414 9.231905e-05
#> IGK 4.5087736 0.40269721 1898 0.5973028 4.043917e-05
#> IGL 4.7761543 0.28333416 784 0.7166658 1.851338e-04
#> TRA 3.7682140 0.07196974 58 0.9280303 1.398601e-02
#> TRB 3.8933793 0.11402336 81 0.8859766 9.174312e-03
#> TRD 0.5004024 0.27807191 2 0.7219281 5.000000e-01
#> TRG NA NA NA NA NA
#>
#> $sample_03
#> diversity clonality richness evenness median
#> IGH 3.3401373 0.5400036 1424 0.4599964 1.032684e-04
#> IGK 5.4716100 0.1767547 770 0.8232453 4.581552e-04
#> IGL 2.5747289 0.6218047 905 0.3781953 6.578731e-05
#> TRA 4.0981274 0.1194323 105 0.8805677 5.917160e-03
#> TRB 3.9120015 0.2282353 159 0.7717647 2.816901e-03
#> TRD NA NA NA NA NA
#> TRG 0.5982696 0.1368794 2 0.8631206 5.000000e-01
all_sample_all_chain_all_metrics_wide_format_dataframe <- all_sample_all_chain_all_metrics_wide_format_dataframe_list %>%
combine_all_sample_repertoire_metrics
all_sample_all_chain_all_metrics_wide_format_dataframe
#> sample_name item_name diversity clonality richness evenness median
#> 1 sample_01 IGH 5.4161872 0.26283295 1552 0.7371670 1.509510e-04
#> 2 sample_01 IGK 5.2677388 0.28931127 1656 0.7106887 9.082240e-05
#> 3 sample_01 IGL 4.8949171 0.25490053 713 0.7450995 4.132231e-04
#> 4 sample_01 TRA 4.3018929 0.06585582 100 0.9341442 6.437768e-03
#> 5 sample_01 TRB 4.8358496 0.08467479 197 0.9153252 3.642987e-03
#> 6 sample_01 TRD 0.6730117 0.02904941 2 0.9709506 5.000000e-01
#> 7 sample_01 TRG 0.6931472 0.00000000 2 1.0000000 5.000000e-01
#> 8 sample_02 IGH 5.3401961 0.28075859 1677 0.7192414 9.231905e-05
#> 9 sample_02 IGK 4.5087736 0.40269721 1898 0.5973028 4.043917e-05
#> 10 sample_02 IGL 4.7761543 0.28333416 784 0.7166658 1.851338e-04
#> 11 sample_02 TRA 3.7682140 0.07196974 58 0.9280303 1.398601e-02
#> 12 sample_02 TRB 3.8933793 0.11402336 81 0.8859766 9.174312e-03
#> 13 sample_02 TRD 0.5004024 0.27807191 2 0.7219281 5.000000e-01
#> 14 sample_02 TRG NA NA NA NA NA
#> 15 sample_03 IGH 3.3401373 0.54000361 1424 0.4599964 1.032684e-04
#> 16 sample_03 IGK 5.4716100 0.17675466 770 0.8232453 4.581552e-04
#> 17 sample_03 IGL 2.5747289 0.62180471 905 0.3781953 6.578731e-05
#> 18 sample_03 TRA 4.0981274 0.11943225 105 0.8805677 5.917160e-03
#> 19 sample_03 TRB 3.9120015 0.22823526 159 0.7717647 2.816901e-03
#> 20 sample_03 TRD NA NA NA NA NA
#> 21 sample_03 TRG 0.5982696 0.13687943 2 0.8631206 5.000000e-01
all_sample_all_chain_individual_metrics_dataframe_list <- all_sample_all_chain_all_metrics_wide_format_dataframe %>%
get_item_name_x_sample_name_for_each_metric
all_sample_all_chain_individual_metrics_dataframe_list
#> $diversity
#> sample_01 sample_02 sample_03
#> IGH 5.4161872 5.3401961 3.3401373
#> IGK 5.2677388 4.5087736 5.4716100
#> IGL 4.8949171 4.7761543 2.5747289
#> TRA 4.3018929 3.7682140 4.0981274
#> TRB 4.8358496 3.8933793 3.9120015
#> TRD 0.6730117 0.5004024 NA
#> TRG 0.6931472 NA 0.5982696
#>
#> $clonality
#> sample_01 sample_02 sample_03
#> IGH 0.26283295 0.28075859 0.5400036
#> IGK 0.28931127 0.40269721 0.1767547
#> IGL 0.25490053 0.28333416 0.6218047
#> TRA 0.06585582 0.07196974 0.1194323
#> TRB 0.08467479 0.11402336 0.2282353
#> TRD 0.02904941 0.27807191 NA
#> TRG 0.00000000 NA 0.1368794
#>
#> $richness
#> sample_01 sample_02 sample_03
#> IGH 1552 1677 1424
#> IGK 1656 1898 770
#> IGL 713 784 905
#> TRA 100 58 105
#> TRB 197 81 159
#> TRD 2 2 NA
#> TRG 2 NA 2
#>
#> $evenness
#> sample_01 sample_02 sample_03
#> IGH 0.7371670 0.7192414 0.4599964
#> IGK 0.7106887 0.5973028 0.8232453
#> IGL 0.7450995 0.7166658 0.3781953
#> TRA 0.9341442 0.9280303 0.8805677
#> TRB 0.9153252 0.8859766 0.7717647
#> TRD 0.9709506 0.7219281 NA
#> TRG 1.0000000 NA 0.8631206
#>
#> $median
#> sample_01 sample_02 sample_03
#> IGH 0.0001509510 9.231905e-05 1.032684e-04
#> IGK 0.0000908224 4.043917e-05 4.581552e-04
#> IGL 0.0004132231 1.851338e-04 6.578731e-05
#> TRA 0.0064377682 1.398601e-02 5.917160e-03
#> TRB 0.0036429872 9.174312e-03 2.816901e-03
#> TRD 0.5000000000 5.000000e-01 NA
#> TRG 0.5000000000 NA 5.000000e-01This step consists of three functions.
# handle repertoire metrics all all the isotypes of IGH chain.
all_sample_IGH_chain_all_metrics_wide_format_dataframe_list <- the_divergent_clonotype_dataframe_list %>%
lapply(., calculate_IGH_isotype_proportion)
all_sample_IGH_chain_all_metrics_wide_format_dataframe_list
#> $sample_01
#> count proportion
#> IGHA 202 0.1828054299
#> IGHD 1 0.0009049774
#> IGHG 813 0.7357466063
#> IGHM 89 0.0805429864
#>
#> $sample_02
#> count proportion
#> IGHA 11 0.0080941869
#> IGHD 1 0.0007358352
#> IGHG 1074 0.7902869757
#> IGHM 273 0.2008830022
#>
#> $sample_03
#> count proportion
#> IGHA 416 0.343517754
#> IGHD 4 0.003303055
#> IGHG 775 0.639966969
#> IGHM 16 0.013212221
all_sample_IGH_chain_all_metrics_wide_format_dataframe <- all_sample_IGH_chain_all_metrics_wide_format_dataframe_list %>%
combine_all_sample_repertoire_metrics
all_sample_IGH_chain_all_metrics_wide_format_dataframe
#> sample_name item_name count proportion
#> 1 sample_01 IGHA 202 0.1828054299
#> 2 sample_01 IGHD 1 0.0009049774
#> 3 sample_01 IGHG 813 0.7357466063
#> 4 sample_01 IGHM 89 0.0805429864
#> 5 sample_02 IGHA 11 0.0080941869
#> 6 sample_02 IGHD 1 0.0007358352
#> 7 sample_02 IGHG 1074 0.7902869757
#> 8 sample_02 IGHM 273 0.2008830022
#> 9 sample_03 IGHA 416 0.3435177539
#> 10 sample_03 IGHD 4 0.0033030553
#> 11 sample_03 IGHG 775 0.6399669694
#> 12 sample_03 IGHM 16 0.0132122213
all_sample_IGH_chain_individual_metrics_dataframe_list <- all_sample_IGH_chain_all_metrics_wide_format_dataframe %>%
get_item_name_x_sample_name_for_each_metric
all_sample_IGH_chain_individual_metrics_dataframe_list
#> $count
#> sample_01 sample_02 sample_03
#> IGHA 202 11 416
#> IGHD 1 1 4
#> IGHG 813 1074 775
#> IGHM 89 273 16
#>
#> $proportion
#> sample_01 sample_02 sample_03
#> IGHA 0.1828054299 0.0080941869 0.343517754
#> IGHD 0.0009049774 0.0007358352 0.003303055
#> IGHG 0.7357466063 0.7902869757 0.639966969
#> IGHM 0.0805429864 0.2008830022 0.013212221The repertoire metrics formula including richness, diversity (Shannon
entropy), evenness (Pielou’s eveness), clonality, and median (frequency
median) were defined as follows, where is the frequency of
in a sample with
unique clonotypes (Khunger,
Rytlewski et al. 2019, Looney,
Topacio-Hall et al. 2020).
is the frequency vector of unique clonotypes in a
sample.
The function calculate_repertoire_metrics is essential
to implement the repertoire metrics formulas
calculate_repertoire_metrics
#> function (named_species_vector)
#> {
#> stopifnot(!duplicated(names(named_species_vector)))
#> species_vector <- named_species_vector
#> frequency_vector <- species_vector/sum(species_vector)
#> shannon_entropy <- -sum(frequency_vector * log(frequency_vector),
#> na.rm = TRUE)
#> richness_count <- length(species_vector)
#> pielou_evenness <- shannon_entropy/log(richness_count)
#> clonality_score <- 1 - pielou_evenness
#> frequency_median <- median(frequency_vector)
#> output_vector <- c(shannon_entropy, clonality_score, richness_count,
#> pielou_evenness, frequency_median)
#> names(output_vector) <- c("diversity", "clonality", "richness",
#> "evenness", "median")
#> output_vector
#> }
#> <bytecode: 0x00000000285ad120>
#> <environment: namespace:rTCRBCRr>The hexagon logo of the package was created with the help of the package hexSticker. The math formula was written with the help of recognition tool MyScript. The latex formula in markdown was inspired by rmd4sci. The code in this study was inspired by the UCSB R tutorial note, LymphoSeq script, and vegan package.
These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.
Health stats visible at Monitor.