Consider the read start in the Cys location

.gitignore

@@ -1,3 +1 @@
-*.txt
-*.fasta
 *.fastq

README.md

@@ -0,0 +1,68 @@
+# locigenesis
+
+locigenesis is a tool that generates a human T-cell receptor (TCR), runs
+it through a sequence reader simulation tool and extracts CDR3.
+
+The goal of this project is to generate both HVR sequences with and
+without sequencing errors, in order to create datasets for a Machine
+Learning algorithm.
+
+## Technologies
+
+-   [immuneSIM](https://github.com/GreiffLab/immuneSIM/): in silico
+    generation of human and mouse BCR and TCR repertoires
+-   [CuReSim](http://www.pegase-biosciences.com/curesim-a-customized-read-simulator/):
+    read simulator that mimics Ion Torrent sequencing
+
+## Installation
+
+This project uses [Nix](https://nixos.org/) to ensure reproducible
+builds.
+
+1.  Install Nix (compatible with MacOS, Linux and
+    [WSL](https://docs.microsoft.com/en-us/windows/wsl/about)):
+
+```bash
+curl -L https://nixos.org/nix/install | sh
+```
+
+2.  Clone the repository:
+
+```bash
+git clone https://git.coolneng.duckdns.org/coolneng/locigenesis
+```
+
+3.  Change the working directory to the project:
+
+```bash
+cd locigenesis
+```
+
+4.  Enter the nix-shell:
+
+```bash
+nix-shell
+```
+
+After running these commands, you will find yourself in a shell that
+contains all the needed dependencies.
+
+## Usage
+
+An execution script that accepts 2 parameters is provided, the following
+command invokes it:
+
+```bash
+./generation.sh <number of sequences> <number of reads>
+```
+
+-   \<number of sequences\>: an integer that specifies the number of
+    different sequences to generate
+-   \<number of reads\>: an integer that specifies the number of reads
+    to perform on each sequence
+
+The script will generate 2 files under the data directory:
+
+|HVR.fastq  | curesim-HVR.fastq |
+|:----:|:-----:|
+|Contains the original CDR3 sequence|Contains CDR3 after the read simulation, with sequencing errors |

README.org

@@ -1,3 +0,0 @@
-* locigenesis
-
-locigenesis is a tool that generates an immune repertoire and runs it through a sequence reader simulation tool, to generate sequencing errors.

generation.sh

@@ -1,7 +1,7 @@
 #!/bin/sh
 
 usage() {
-	echo "usage: generation.sh <number of sequences> <sequencing runs>"
+	echo "usage: generation.sh <number of sequences> <number of reads>"
 	exit 1
 }
 
@@ -10,15 +10,13 @@ if [ $# != 2 ]; then
 fi
 
 sequences=$1
-sequencing_runs=$2
+number_of_reads=$2
-read_mean_size=350
-read_variance_size=0.0
 data_directory="data/"
-fasta=".fasta"
 fastq=".fastq"
 filename="sequence"
 prefix="curesim_"
 
-Rscript src/repertoire.r "$sequences" "$sequencing_runs"
+Rscript src/repertoire.r "$sequences" "$number_of_reads" &&
-java -jar tools/CuReSim.jar -m "$read_mean_size" -sd "$read_variance_size" -f "$data_directory$filename$fasta" -o "$data_directory$prefix$filename$fastq"
+	CuReSim -f "$data_directory$filename$fastq" -o "$data_directory$prefix$filename$fastq"
+Rscript src/alignment.r
 rm "$data_directory/log.txt"

nix/sources.json

@@ -17,10 +17,10 @@
         "homepage": "",
         "owner": "NixOS",
         "repo": "nixpkgs",
-        "rev": "6f1ce38d0c0b1b25727d86637fd2f3baf7b0f1f6",
+        "rev": "a565a2165ab6e195d7c105a8416b8f4b4d0349a4",
-        "sha256": "16da722vqn96k1scls8mr8l909hl66r7y4ik6sad4ms3vmxbkbb3",
+        "sha256": "1x90qm533lh8xh172rqfcj3pwg8imyx650xgr41rqppmm6fli4w1",
         "type": "tarball",
-        "url": "https://github.com/NixOS/nixpkgs/archive/6f1ce38d0c0b1b25727d86637fd2f3baf7b0f1f6.tar.gz",
+        "url": "https://github.com/NixOS/nixpkgs/archive/a565a2165ab6e195d7c105a8416b8f4b4d0349a4.tar.gz",
         "url_template": "https://github.com/<owner>/<repo>/archive/<rev>.tar.gz"
     }
 }

shell.nix

@@ -2,14 +2,29 @@
 
 with pkgs;
 
-mkShell {
+let
-  buildInputs = [
+  CuReSim = stdenv.mkDerivation rec {
-    R
+    name = "CuReSim";
-    rPackages.immuneSIM
+    version = "1.3";
-    rPackages.Biostrings
+    src = fetchzip {
-    jdk
+      url =
-    # Development tools
+        "http://www.pegase-biosciences.com/wp-content/uploads/2015/08/${name}${version}.zip";
-    rPackages.languageserver
+      sha256 = "1hvlpgy4haqgqq52mkxhcl9i1fx67kgwi6f1mijvqzk0xff77hkp";
-    rPackages.lintr
+      stripRoot = true;
-  ];
+      extraPostFetch = ''
+        chmod go-w $out
+      '';
+    };
+
+    nativeBuildInputs = [ makeWrapper ];
+
+    installPhase = ''
+      mkdir -pv $out/share/java $out/bin
+      cp -r ${src} $out/share/java/${name}
+      makeWrapper ${jre}/bin/java $out/bin/CuReSim --add-flags "-jar $out/share/java/${name}/${name}.jar"
+    '';
+  };
+in mkShell {
+  buildInputs =
+    [ R rPackages.immuneSIM rPackages.Biostrings rPackages.stringr CuReSim ];
 }

src/alignment.r

@@ -0,0 +1,153 @@
+library(Biostrings)
+library(parallel)
+
+#' Import and process the TCR and VJ sequences
+#'
+#' @param file A file path with the sequences after applying a read simulator
+#' @return A \code{list} with the TCR sequences and VJ sequences
+parse_data <- function(file) {
+  reversed_sequences <- Biostrings::readQualityScaledDNAStringSet(file)
+  sequences <- Biostrings::reverseComplement(reversed_sequences)
+  vj_segments <- union(
+    readRDS("data/v_segments.rds"),
+    readRDS("data/j_segments_phe.rds")
+  )
+  return(list(sequences, vj_segments))
+}
+
+#' Extracts the VJ metadata from the sequences read identifier
+#'
+#' @param metadata The read identifier of a sequence
+#' @return A \code{list} with the V and J gene identifier
+parse_metadata <- function(metadata) {
+  id_elements <- unlist(strsplit(metadata, split = " "))
+  v_identifier <- id_elements[2]
+  j_identifier <- id_elements[3]
+  return(list(v_id = v_identifier, j_id = j_identifier))
+}
+
+#' Fetches the sequence that matches the VJ gene identifier
+#'
+#' @param names The names of the VJ sequences
+#' @param vdj_segments A \code{DNAStringSet} containing the VJ sequences
+#' @param id The read identifier of a sequence
+#' @return A \code{character} containing the gene sequence
+match_id_sequence <- function(names, vdj_segments, id) {
+  matches <- grep(names, pattern = id)
+  if(id == "TRBJ2-2"){
+    row <- matches[2]
+  } else {
+    row <- matches[1]
+  }
+  return(as.character(vdj_segments[row]))
+}
+
+#' Gets the V and J sequences for a particular read identifier
+#'
+#' @param metadata The read identifier of a sequence
+#' @param names The names of the VJ sequences
+#' @param vdj_segments A \code{DNAStringSet} containing the VJ sequences
+#' @return A \code{list} with the V and J sequences
+get_vj_sequence <- function(metadata, names, vdj_segments) {
+  identifiers <- parse_metadata(metadata)
+  v_sequence <- match_id_sequence(names, vdj_segments, id = identifiers["v_id"])
+  j_sequence <- match_id_sequence(names, vdj_segments, id = identifiers["j_id"])
+  return(list(v_seq = v_sequence, j_seq = j_sequence))
+}
+
+#' Obtains the VJ sequences for all the TCR sequences
+#'
+#' @param sequences A \code{QualityScaledDNAStringSet} with the TCR sequences
+#' @param vdj_segments A \code{DNAStringSet} containing the VJ sequences
+#' @return A \code{data.frame} with the V and J sequences
+fetch_vj_sequences <- function(sequences, vdj_segments) {
+  vj_sequences <- sapply(names(sequences),
+    names(vdj_segments),
+    vdj_segments,
+    FUN = get_vj_sequence
+  )
+  results <- data.frame(t(vj_sequences))
+  return(results)
+}
+
+#' Perform a pairwise alignment of a sequence with the canonical V or J sequence
+#'
+#' @param sequence A \code{DNAString} containing the TCR sequences
+#' @param vdj_segment A \code{DNAString} containing the V or J sequence
+#' @return A \code{PairwiseAlignments}
+align_sequence <- function(sequence, vdj_segment) {
+  return(Biostrings::pairwiseAlignment(
+    subject = sequence,
+    pattern = vdj_segment,
+    type = "global-local",
+    gapOpening = 1
+  ))
+}
+
+#' Computes the coordinate shift of the Cysteine due to indels
+#'
+#' @param insertion An \code{IRanges} containing the insertions
+#' @param deletion An \code{IRanges} containing the deletions
+#' @param cys A \code{list} with the Cysteine coordinates
+#' @param alignment A \code{PairwiseAlignments}
+#' @return A \code{list} with the delta of the Cysteine coordinates
+handle_indels <- function(insertion, deletion, cys, alignment) {
+  ins_start <- sum(Biostrings::width(deletion[start(deletion) <= cys$start]))
+  ins_end <- sum(Biostrings::width(deletion[end(deletion) <= cys$end]))
+  shift_num <- c(0, cumsum(Biostrings::width(insertion))[-length(ins_start)])
+  shifted_ins <- IRanges::shift(insertion, shift_num)
+  gaps <- sum(width(shifted_ins[end(shifted_ins) < cys$start + ins_start])) +
+    nchar(stringr::str_extract(alignedSubject(alignment), "^-*"))
+  return(list("start" = ins_start - gaps, "end" = ins_end - gaps))
+}
+
+#' Find the coordinates of the first Cysteine of the HVR
+#'
+#' @param alignment A \code{PairwiseAlignments}
+#' @return A \code{list} with the Cysteine coordinates
+get_cys_coordinates <- function(alignment) {
+  cys <- list("start" = 310, "end" = 312)
+  insertion <- unlist(Biostrings::insertion(alignment))
+  deletion <- unlist(Biostrings::deletion(alignment))
+  delta_coordinates <- handle_indels(insertion, deletion, cys, alignment)
+  read_start <- unlist(start(Biostrings::Views(alignment)))
+  cys_start <- cys$start + delta_coordinates$start + read_start - 1
+  cys_end <- cys$end + delta_coordinates$end + read_start
+  return(list("start" = cys_start, "end" = cys_end))
+}
+
+#' Delimit the hypervariable region (HVR) for each TCR sequence
+#'
+#' @param sequences A \code{QualityScaledDNAStringSet} with the TCR sequences
+#' @param vdj_segments A \code{DNAStringSet} containing the VJ sequences
+#' @param cores Number of cores to apply multiprocessing
+#' @return A \code{QualityScaledDNAStringSet} containing the HVR
+get_hvr_sequences <- function(sequences, vdj_segments, cores = detectCores()) {
+  df <- fetch_vj_sequences(sequences, vdj_segments)
+  v_alignment <- parallel::mcmapply(sequences,
+    df$v_seq,
+    FUN = align_sequence,
+    mc.cores = cores
+  )
+  cys_coordinates <- parallel::mclapply(v_alignment, FUN = get_cys_coordinates)
+  cys_df <- as.data.frame(do.call(rbind, cys_coordinates))
+  remaining <- Biostrings::subseq(sequences, start = unlist(cys_df$end) + 1)
+  j_alignment <- parallel::mcmapply(remaining,
+    df$j_seq,
+    FUN = align_sequence,
+    mc.cores = cores
+  )
+  j_start <- parallel::mclapply(
+    j_alignment,
+    function(x) start(Biostrings::Views(x)),
+    mc.cores = cores
+  )
+  hvr_start <- unlist(cys_df$start)
+  hvr_end <- unlist(cys_df$start) + unlist(j_start) + 2
+  hvr <- Biostrings::subseq(sequences, start = hvr_start, end = hvr_end)
+  return(hvr)
+}
+
+data <- parse_data(file = "data/curesim_sequence.fastq")
+hvr <- get_hvr_sequences(sequences = data[[1]], vdj_segments = data[[2]])
+Biostrings::writeXStringSet(hvr, "data/curesim-HVR.fastq", format = "fastq")

src/repertoire.r

@@ -1,6 +1,10 @@
 library(immuneSIM)
 library(Biostrings)
 
+#' Generate the beta chain of a human T-cell receptor (TCR)
+#'
+#' @param number_of_sequences Number of different sequences to generate
+#' @return A \code{data.frame} with the sequences, V and J genes and CDR3
 generate_repertoire <- function(number_of_sequences) {
   return(immuneSIM(
     number_of_seqs = number_of_sequences,
@@ -10,42 +14,44 @@ generate_repertoire <- function(number_of_sequences) {
   ))
 }
 
-amplify_rows <- function(data, column, factor) {
+#' Saves the sequences and CDR3 to FASTQ files
-  if (column == "sequence") {
+#'
-    dna_string <- Biostrings::DNAStringSet(data)
+#' @param data A \code{data.frame} with the preprocessed TCR sequences and CDR3
-    reverse_complement <- Biostrings::reverseComplement(dna_string)
+save_data <- function(data) {
-    return(rep(reverse_complement, factor))
+  Biostrings::writeXStringSet(data$sequence,
-  }
+    "data/sequence.fastq",
-  return(rep(data, factor))
+    format = "fastq"
+  )
+  Biostrings::writeXStringSet(data$junction, "data/HVR.fastq", format = "fastq")
 }
 
-save_data <- function(data, name) {
+#' Applies the reverse complement and amplifies the number of sequences
-  if (name == "sequence") {
+#'
-    file_name <- paste("data/", name, ".fasta", sep = "")
+#' @param data A \code{data.frame} containing the TCR sequences and CDR3
-    Biostrings::writeXStringSet(data, file_name, format = "fasta")
+#' @param reads Number of times to amplify each sequence
-  } else {
+#' @return A \code{data.frame} with reverse complement sequences and VJ metadata
-    file_name <- paste("data/", name, ".txt", sep = "")
+process_data <- function(data, reads) {
-    cat(data, file = file_name, sep = "\n")
+  dna_sequence <- Biostrings::DNAStringSet(data$sequence)
-  }
+  data$sequence <- Biostrings::reverseComplement(dna_sequence)
+  names(data$sequence) <- paste(rownames(data), data$v_call, data$j_call, " ")
+  data$junction <- Biostrings::DNAStringSet(data$junction)
+  names(data$junction) <- rownames(data)
+  amplified_data <- data[rep(seq_len(nrow(data)), reads), ]
+  return(amplified_data)
 }
 
-process_data <- function(repertoire, sequencing_runs) {
+#' Checks the number of command line arguments and captures them
-  columns <- c("sequence", "v_call", "j_call")
+#'
-  data <- repertoire[, columns]
+#' @return A \code{vector} containing the command line arguments
-  amplified_data <- mapply(data, names(data), sequencing_runs, FUN = amplify_rows)
+parse_cli_arguments <- function() {
-  invisible(mapply(amplified_data, names(amplified_data), FUN = save_data))
+  args <- commandArgs(trailingOnly = TRUE)
-}
-
-parse_cli_arguments <- function(args) {
   if (length(args) != 2) {
-    stop("usage: repertoire.r <number of sequences> <sequencing_runs>")
+    stop("usage: repertoire.r <number of sequences> <number of reads>")
   }
-  return(c(args[1], args[2]))
+  return(args)
 }
 
-args <- commandArgs(trailingOnly = TRUE)
+args <- parse_cli_arguments()
-arguments <- parse_cli_arguments(args)
+repertoire <- generate_repertoire(number_of_sequences = as.integer(args[1]))
-number_of_sequences <- as.integer(arguments[1])
+data <- process_data(data = repertoire, reads = args[2])
-sequencing_runs <- as.integer(arguments[2])
+save_data(data)
-repertoire <- generate_repertoire(number_of_sequences)
-process_data(repertoire, sequencing_runs)