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0.1.1
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e8f03189c2
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f4b7a41599
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9e8beefd38
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@@ -1,46 +0,0 @@
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#+TITLE: locigenesis
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#+AUTHOR: Amin Kasrou Aouam
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#+DATE: 2021-03-10
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* Sequence alignment
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Our generated sequences contain the full VJ region, but we are only interested in the CDR3 (Complementarity-determining region). We will proceed by delimiting CDR3, using the known sequences of V and J.
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#+begin_src R :results value silent
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v_segments <- readRDS("data/v_segments.rds")
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j_segments <- readRDS("data/j_segments_phe.rds")
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#+end_src
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#+begin_src R
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print(v_segments)
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print(j_segments)
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#+end_src
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#+RESULTS:
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#+begin_example
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A DNAStringSet instance of length 147
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width seq names
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[1] 326 GATACTGGAATTACCCAGACAC...ATCTCTGCACCAGCAGCCAAGA TRBV1*01_P
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[2] 326 GATGCTGAAATCACCCAGAGCC...ATTTCTGCGCCAGCAGTGAGTC TRBV10-1*01_F
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[3] 326 GATGCTGAAATCACCCAGAGCC...ATTTCTGCGCCAGCAGTGAGTC TRBV10-1*02_F
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[4] 326 GATGCTGGAATCACCCAGAGCC...ATTTCTGCGCCAGCAGTGAGTC TRBV10-2*01_F
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[5] 326 GATGCTGGAATCACCCAGAGCC...ATTTCTGCGCCAGCAGTGAGTC TRBV10-2*02_F
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... ... ...
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[143] 324 GATACTGGAGTCTCCCAGAACC...GTATCTCTGTGCCAGCACGTTG TRBV7-9*06_(F)
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[144] 323 .........................TGTATCTCTGTGCCAGCAGCAG TRBV7-9*07_(F)
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[145] 325 GATTCTGGAGTCACACAAACCC...TATTTCTGTGCCAGCAGCGTAG TRBV9*01_F
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[146] 325 GATTCTGGAGTCACACAAACCC...TATTTCTGTGCCAGCAGCGTAG TRBV9*02_F
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[147] 321 GATTCTGGAGTCACACAAACCC...TTTGTATTTCTGTGCCAGCAGC TRBV9*03_(F)
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A DNAStringSet instance of length 16
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width seq names
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[1] 32 TGGGCGTCTGGGCGGAGGACTCCTGGTTCTGG TRBJ2-2P*01_ORF
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[2] 31 TTTGGAGAGGGAAGTTGGCTCACTGTTGTAG TRBJ1-3*01_F
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[3] 31 TTTGGTGATGGGACTCGACTCTCCATCCTAG TRBJ1-5*01_F
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[4] 31 TTTGGCAGTGGAACCCAGCTCTCTGTCTTGG TRBJ1-4*01_F
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[5] 31 TTCGGTTCGGGGACCAGGTTAACCGTTGTAG TRBJ1-2*01_F
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... ... ...
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[12] 31 TTTGGCCCAGGCACCCGGCTGACAGTGCTCG TRBJ2-3*01_F
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[13] 31 TTCGGGCCAGGCACGCGGCTCCTGGTGCTCG TRBJ2-5*01_F
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[14] 31 TTCGGGCCAGGGACACGGCTCACCGTGCTAG TRBJ2-1*01_F
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[15] 31 TTCGGGCCGGGCACCAGGCTCACGGTCACAG TRBJ2-7*01_F
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[16] 31 GTCGGGCCGGGCACCAGGCTCACGGTCACAG TRBJ2-7*02_ORF
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#+end_example
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@@ -1,6 +1,10 @@
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library(Biostrings)
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library(parallel)
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#' Import and process the TCR and VJ sequences
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#'
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#' @param file A file path with the sequences after applying a read simulator
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#' @return A \code{list} with the TCR sequences and VJ sequences
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parse_data <- function(file) {
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reversed_sequences <- Biostrings::readQualityScaledDNAStringSet(file)
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sequences <- Biostrings::reverseComplement(reversed_sequences)
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@@ -11,6 +15,10 @@ parse_data <- function(file) {
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return(list(sequences, vj_segments))
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}
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#' Extracts the VJ metadata from the sequences read identifier
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#'
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#' @param metadata The read identifier of a sequence
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#' @return A \code{list} with the V and J gene identifier
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parse_metadata <- function(metadata) {
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id_elements <- unlist(strsplit(metadata, split = " "))
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v_identifier <- id_elements[2]
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@@ -18,12 +26,24 @@ parse_metadata <- function(metadata) {
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return(list(v_id = v_identifier, j_id = j_identifier))
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}
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#' Fetches the sequence that matches the VJ gene identifier
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#'
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#' @param names The names of the VJ sequences
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#' @param vdj_segments A \code{DNAStringSet} containing the VJ sequences
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#' @param id The read identifier of a sequence
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#' @return A \code{character} containing the gene sequence
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match_id_sequence <- function(names, vdj_segments, id) {
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matches <- grep(names, pattern = id)
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row <- matches[1]
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return(as.character(vdj_segments[row]))
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}
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#' Gets the V and J sequences for a particular read identifier
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#'
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#' @param metadata The read identifier of a sequence
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#' @param names The names of the VJ sequences
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#' @param vdj_segments A \code{DNAStringSet} containing the VJ sequences
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#' @return A \code{list} with the V and J sequences
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get_vj_sequence <- function(metadata, names, vdj_segments) {
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identifiers <- parse_metadata(metadata)
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v_sequence <- match_id_sequence(names, vdj_segments, id = identifiers["v_id"])
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@@ -31,6 +51,11 @@ get_vj_sequence <- function(metadata, names, vdj_segments) {
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return(list(v_seq = v_sequence, j_seq = j_sequence))
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}
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#' Obtains the VJ sequences for all the TCR sequences
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#'
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#' @param sequences A \code{QualityScaledDNAStringSet} with the TCR sequences
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#' @param vdj_segments A \code{DNAStringSet} containing the VJ sequences
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#' @return A \code{data.frame} with the V and J sequences
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fetch_vj_sequences <- function(sequences, vdj_segments) {
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vj_sequences <- sapply(names(sequences),
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names(vdj_segments),
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@@ -41,6 +66,11 @@ fetch_vj_sequences <- function(sequences, vdj_segments) {
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return(results)
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}
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#' Perform a pairwise alignment of a sequence with the canonical V or J sequence
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#'
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#' @param sequence A \code{DNAString} containing the TCR sequences
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#' @param vdj_segment A \code{DNAString} containing the V or J sequence
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#' @return A \code{PairwiseAlignments}
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align_sequence <- function(sequence, vdj_segment) {
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return(Biostrings::pairwiseAlignment(
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subject = sequence,
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@@ -50,6 +80,13 @@ align_sequence <- function(sequence, vdj_segment) {
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))
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}
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#' Computes the coordinate shift of the Cysteine due to indels
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#'
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#' @param insertion An \code{IRanges} containing the insertions
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#' @param deletion An \code{IRanges} containing the deletions
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#' @param cys A \code{list} with the Cysteine coordinates
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#' @param alignment A \code{PairwiseAlignments}
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#' @return A \code{list} with the delta of the Cysteine coordinates
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handle_indels <- function(insertion, deletion, cys, alignment) {
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ins_start <- sum(Biostrings::width(deletion[start(deletion) <= cys$start]))
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ins_end <- sum(Biostrings::width(deletion[end(deletion) <= cys$end]))
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@@ -60,6 +97,10 @@ handle_indels <- function(insertion, deletion, cys, alignment) {
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return(list("start" = ins_start - gaps, "end" = ins_end - gaps))
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}
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#' Find the coordinates of the first Cysteine of the HVR
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#'
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#' @param alignment A \code{PairwiseAlignments}
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#' @return A \code{list} with the Cysteine coordinates
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get_cys_coordinates <- function(alignment) {
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cys <- list("start" = 310, "end" = 312)
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insertion <- unlist(Biostrings::insertion(alignment))
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@@ -70,6 +111,12 @@ get_cys_coordinates <- function(alignment) {
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return(list("start" = cys_start, "end" = cys_end))
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}
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#' Delimit the hypervariable region (HVR) for each TCR sequence
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#'
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#' @param sequences A \code{QualityScaledDNAStringSet} with the TCR sequences
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#' @param vdj_segments A \code{DNAStringSet} containing the VJ sequences
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#' @param cores Number of cores to apply multiprocessing
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#' @return A \code{QualityScaledDNAStringSet} containing the HVR
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get_hvr_sequences <- function(sequences, vdj_segments, cores = detectCores()) {
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df <- fetch_vj_sequences(sequences, vdj_segments)
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v_alignment <- parallel::mcmapply(sequences,
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@@ -1,6 +1,10 @@
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library(immuneSIM)
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library(Biostrings)
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#' Generate the beta chain of a human T-cell receptor (TCR)
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#'
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#' @param number_of_sequences Number of different sequences to generate
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#' @return A \code{data.frame} with the sequences, V and J genes and CDR3
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generate_repertoire <- function(number_of_sequences) {
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return(immuneSIM(
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number_of_seqs = number_of_sequences,
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@@ -10,6 +14,9 @@ generate_repertoire <- function(number_of_sequences) {
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))
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}
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#' Saves the sequences and CDR3 to FASTQ files
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#'
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#' @param data A \code{data.frame} with the preprocessed TCR sequences and CDR3
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save_data <- function(data) {
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Biostrings::writeXStringSet(data$sequence,
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"data/sequence.fastq",
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@@ -18,6 +25,11 @@ save_data <- function(data) {
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Biostrings::writeXStringSet(data$junction, "data/HVR.fastq", format = "fastq")
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}
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#' Applies the reverse complement and amplifies the number of sequences
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#'
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#' @param data A \code{data.frame} containing the TCR sequences and CDR3
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#' @param reads Number of times to amplify each sequence
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#' @return A \code{data.frame} with reverse complement sequences and VJ metadata
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process_data <- function(data, reads) {
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dna_sequence <- Biostrings::DNAStringSet(data$sequence)
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data$sequence <- Biostrings::reverseComplement(dna_sequence)
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@@ -28,6 +40,9 @@ process_data <- function(data, reads) {
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return(amplified_data)
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}
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#' Checks the number of command line arguments and captures them
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#'
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#' @return A \code{vector} containing the command line arguments
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parse_cli_arguments <- function() {
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args <- commandArgs(trailingOnly = TRUE)
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if (length(args) != 2) {
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