CodonTransformer

Table of Contents

• Overview
• Use Case
• Installation
• Finetuning
• Key Features
  • CodonData
  • CodonPrediction
  • CodonEvaluation
  • CodonUtils
  • CodonJupyter
• Contribution
• Citation
  
  

Abstract

The genetic code is degenerate allowing a multitude of possible DNA sequences to encode the same protein. This degeneracy impacts the efficiency of heterologous protein production due to the codon usage preferences of each organism. The process of tailoring organism-specific synonymous codons, known as codon optimization, must respect local sequence patterns that go beyond global codon preferences. As a result, the search space faces a combinatorial explosion that makes exhaustive exploration impossible. Nevertheless, throughout the diverse life on Earth, natural selection has already optimized the sequences, thereby providing a rich source of data allowing machine learning algorithms to explore the underlying rules. Here, we introduce CodonTransformer, a multispecies deep learning model trained on over 1 million DNA-protein pairs from 164 organisms spanning all kingdoms of life. The model demonstrates context-awareness thanks to the attention mechanism and bidirectionality of the Transformers we used, and to a novel sequence representation that combines organism, amino acid, and codon encodings. CodonTransformer generates host-specific DNA sequences with natural-like codon distribution profiles and with negative cis-regulatory elements. This work introduces a novel strategy of Shared Token Representation and Encoding with Aligned Multi-masking (STREAM) and provides a state-of-the-art codon optimization framework with a customizable open-access model and a user-friendly interface.

Use Case

For a user-friendly interface, check out our Google Colab Notebook.

After installing CodonTransformer, you can use:

import torch
from transformers import AutoTokenizer, BigBirdForMaskedLM
from CodonTransformer.CodonPrediction import predict_dna_sequence
from CodonTransformer.CodonJupyter import format_model_output
device = torch.device("cuda" if torch.cuda.is_available() else "cpu")


# Load model and tokenizer
tokenizer = AutoTokenizer.from_pretrained("adibvafa/CodonTransformer")
model = BigBirdForMaskedLM.from_pretrained("adibvafa/CodonTransformer").to(device)


# Set your input data
protein = "MALWMRLLPLLALLALWGPDPAAAFVNQHLCGSHLVEALYLVCGERGFFYTPKTRREAEDLQVGQVELGG"
organism = "Escherichia coli general"


# Predict with CodonTransformer
output = predict_dna_sequence(
    protein=protein,
    organism=organism,
    device=device,
    tokenizer=tokenizer,
    model=model,
    attention_type="original_full",
    deterministic=True
)
print(format_model_output(output))

The output is:

-----------------------------
|          Organism         |
-----------------------------
Escherichia coli general

-----------------------------
|       Input Protein       |
-----------------------------
MALWMRLLPLLALLALWGPDPAAAFVNQHLCGSHLVEALYLVCGERGFFYTPKTRREAEDLQVGQVELGG

-----------------------------
|      Processed Input      |
-----------------------------
M_UNK A_UNK L_UNK W_UNK M_UNK R_UNK L_UNK L_UNK P_UNK L_UNK L_UNK A_UNK L_UNK L_UNK A_UNK L_UNK W_UNK G_UNK P_UNK D_UNK P_UNK A_UNK A_UNK A_UNK F_UNK V_UNK N_UNK Q_UNK H_UNK L_UNK C_UNK G_UNK S_UNK H_UNK L_UNK V_UNK E_UNK A_UNK L_UNK Y_UNK L_UNK V_UNK C_UNK G_UNK E_UNK R_UNK G_UNK F_UNK F_UNK Y_UNK T_UNK P_UNK K_UNK T_UNK R_UNK R_UNK E_UNK A_UNK E_UNK D_UNK L_UNK Q_UNK V_UNK G_UNK Q_UNK V_UNK E_UNK L_UNK G_UNK G_UNK __UNK

-----------------------------
|       Predicted DNA       |
-----------------------------
ATGGCTTTATGGATGCGTCTGCTGCCGCTGCTGGCGCTGCTGGCGCTGTGGGGCCCGGACCCGGCGGCGGCGTTTGTGAATCAGCACCTGTGCGGCAGCCACCTGGTGGAAGCGCTGTATCTGGTGTGCGGTGAGCGCGGCTTCTTCTACACGCCCAAAACCCGCCGCGAAGCGGAAGATCTGCAGGTGGGCCAGGTGGAGCTGGGCGGCTAA

Generating Multiple Variable Sequences

Set deterministic=False to generate variable sequences. Control the variability using temperature:

• temperature: (recommended between 0.2 and 0.8)
  • Lower values (e.g., 0.2): More conservative predictions
  • Higher values (e.g., 0.8): More diverse predictions

Using high temperatures (e.g. more than 1) might result in prediction of DNA sequences that do not translate to the input protein.
You can set match_protein=True to ensure predicted DNA sequences translate to the input protein.
Generate multiple sequences by setting num_sequences to a value greater than 1.

Batch Inference

You can use the inference template to setup your dataset for batch inference in Google Colab. A sample dataset is provided under \demo . A typical inference might take 1-3 seconds based on available compute.

Arguments of predict_dna_sequence

Argument	Type	Description	Default
protein	str	Input protein sequence	Required
organism	Union[int, str]	Organism ID (integer) or name (string) (e.g., “Escherichia coli general”)	Required
device	torch.device	PyTorch device object specifying whether to run on CPU or GPU	Required
tokenizer	Union[str, PreTrainedTokenizerFast, None]	Either a file path to load tokenizer from, a pre-loaded tokenizer object, or None to load from HuggingFace’s “adibvafa/CodonTransformer”	None
model	Union[str, torch.nn.Module, None]	Either a file path to load model from, a pre-loaded model object, or None to load from HuggingFace’s “adibvafa/CodonTransformer”	None
attention_type	str	Type of attention mechanism to use in model - ‘block_sparse’ for memory efficient or ‘original_full’ for standard attention	"original_full"
deterministic	bool	If True, uses deterministic decoding (picks most likely tokens). If False, samples tokens based on probabilities adjusted by temperature	True
temperature	float	Controls randomness in non-deterministic mode. Lower values (0.2) are conservative and pick high probability tokens, while higher values (0.8) allow more diversity. Must be positive	0.2
top_p	float	Nucleus sampling threshold - only tokens with cumulative probability up to this value are considered. Balances diversity and quality of predictions. Must be between 0 and 1	0.95
num_sequences	int	Number of different DNA sequences to generate. Only works when deterministic=False. Each sequence will be sampled based on the temperature and top_p parameters. Must be positive	1
match_protein	bool	Constrains predictions to only use codons that translate back to the exact input protein sequence. Only recommended when using high temperatures or error prone input proteins (e.g. not starting with methionine or having numerous repetitions)	False

Returns: Union[DNASequencePrediction, List[DNASequencePrediction]] containing predicted DNA sequence(s) and metadata.

Installation

Install CodonTransformer via pip:

pip install CodonTransformer

Or clone the repository:

git clone https://github.com/adibvafa/CodonTransformer.git
cd CodonTransformer
pip install -r requirements.txt

The package requires python>=3.9, supports all major operating systems, and takes about 10-30 seconds depending on already installed requirements, availabe here.

Finetuning CodonTransformer

To finetune CodonTransformer on your own data, follow these steps:

1. Prepare your dataset

   Create a CSV file with the following columns:

   • dna: DNA sequences (string, preferably uppercase ATCG)
   • protein: Protein sequences (string, preferably uppercase amino acid letters)
   • organism: Target organism (string or int, must be from ORGANISM2ID in CodonUtils)

   Note:

   • Use organisms from the FINE_TUNE_ORGANISMS list for best results.
   • For E. coli, use Escherichia coli general.
   • DNA sequences should ideally contain only A, T, C, and G. Ambiguous codons are replaced with ‘UNK’ for tokenization.
   • Protein sequences should contain standard amino acid letters from AMINO_ACIDS in CodonUtils. Ambiguous amino acids are replaced according to the AMBIGUOUS_AMINOACID_MAP in CodonUtils.
   • End your DNA sequences with a stop codon from STOP_CODONS in CodonUtils. If not present, a ‘UNK’ stop codon will be addded in preprocessing.
   • End your protein sequence with _ or *. If either is not present, a _ will be added in preprocessing.
     

2. Prepare training data

   Use the prepare_training_data function from CodonData to prepare training data from your dataset.

   from CodonTransformer.CodonData import prepare_training_data
   prepare_training_data('your_data.csv', 'your_dataset_directory/training_data.json')
   

3. Run the finetuning script Execute finetune.py with appropriate arguments: (an example)

    python finetune.py \
       --dataset_dir 'your_dataset_directory/training_data.json' \
       --checkpoint_dir 'your_checkpoint_directory' \
       --checkpoint_filename 'finetune.ckpt' \
       --batch_size 6 \
       --max_epochs 15 \
       --num_workers 5 \
       --accumulate_grad_batches 1 \
       --num_gpus 4 \
       --learning_rate 0.00005 \
       --warmup_fraction 0.1 \
       --save_every_n_steps 512 \
       --seed 23
   

   This script automatically loads the pretrained model from Hugging Face and finetunes it on your dataset. For an example of a SLURM job request, see the slurm directory in the repository.
   
   

Handling Ambiguous Amino Acids

CodonTransformer provides a flexible system for handling ambiguous amino acids through the ProteinConfig class. By default, CodonUtils includes a predefined mapping for ambiguous amino acids, but users can customize this behavior:

from CodonTransformer.CodonUtils import ProteinConfig

# Configure protein preprocessing
config = ProteinConfig()
config.set('ambiguous_aminoacid_behavior', 'standardize_random')
config.set('ambiguous_aminoacid_map_override', {'X': ['A', 'G', 'S']})

# Run CodonTransformer
...

Options for ambiguous_aminoacid_behavior:

• standardize_random (default): Randomly selects a random amino acid from the mapping list.
• standardize_deterministic: Selects the first amino acid from the mapping list.
• raise_error: Treats ambiguous amino acids as invalid.

Users can override the default mapping with ambiguous_aminoacid_map_override.

Organisms

This project utilizes a dataset of 164 distinct organisms for training and fine-tuning. The full dataset, including genomic sequences and codon adaptation indices, can be found at Zenodo (DOI: 10.5281/zenodo.12509224).

Summary by Kingdom

Kingdom	Number of Organisms
Bacteria	142
Archaea	11
Plantae	5
Animalia	5
Fungi	1
Total	164

Detailed Breakdown by Clade

Animalia

Class	Number of Organisms	Organism Names
Mammalia	2	Homo sapiens, Mus musculus
Insecta	1	Drosophila melanogaster
Actinopterygii	1	Danio rerio (zebrafish)
Chromadorea	1	Caenorhabditis elegans

Plantae

The list includes two plant species, a green alga, and their corresponding chloroplasts, which are treated as separate entries in the dataset.

Phylum	Class	Number of Organisms	Organism Names
Tracheophyta	Magnoliopsida	3	Arabidopsis thaliana, Nicotiana tabacum, Nicotiana tabacum chloroplast
Chlorophyta	Chlorophyceae	2	Chlamydomonas reinhardtii, Chlamydomonas reinhardtii chloroplast

Fungi

Phylum	Class	Number of Organisms	Organism Name
Ascomycota	Saccharomycetes	1	Saccharomyces cerevisiae

Archaea

The archaeal organisms in this dataset are all extremophiles.

Phylum	Class	Number of Organisms	Genera
Euryarchaeota	Thermococci	10	Pyrococcus, Thermococcus
Crenarchaeota	Thermoprotei	1	Saccharolobus

Bacteria

The vast majority of the organisms in the dataset are bacteria, primarily from the phylum Pseudomonadota (formerly Proteobacteria).

Phylum	Number of Organisms	Notable Genera
Pseudomonadota	141	Escherichia, Salmonella, Klebsiella, Pseudomonas, Yersinia, Serratia, Enterobacter, Proteus, etc.
Bacillota	1	Bacillus

Full Organism List

The model supports the following 164 organisms. Organisms can be referenced by their name or by their corresponding ID (0-163) when using the tool.

Arabidopsis thaliana	Enterobacter hormaechei	Klebsiella variicola	Proteus penneri
Atlantibacter hermannii	Enterobacter kobei	Kosakonia cowanii	Proteus terrae subsp. cibarius
Bacillus subtilis	Enterobacter ludwigii	Kosakonia radicincitans	Proteus vulgaris
Brenneria goodwinii	Enterobacter mori	Leclercia adecarboxylata	Providencia alcalifaciens
Buchnera aphidicola (Schizaphis graminum)	Enterobacter quasiroggenkampii	Lelliottia amnigena	Providencia heimbachae
Caenorhabditis elegans	Enterobacter roggenkampii	Lonsdalea populi	Providencia rettgeri
Candidatus Erwinia haradaeae	Enterobacter sichuanensis	Moellerella wisconsensis	Providencia rustigianii
Candidatus Hamiltonella defensa 5AT (Acyrthosiphon pisum)	Erwinia amylovora CFBP1430	Morganella morganii	Providencia stuartii
Chlamydomonas reinhardtii	Erwinia persicina	Mus musculus	Providencia thailandensis
Chlamydomonas reinhardtii chloroplast	Escherichia albertii	Nicotiana tabacum	Pseudomonas putida
Citrobacter amalonaticus	Escherichia coli general	Nicotiana tabacum chloroplast	Pyrococcus furiosus
Citrobacter braakii	Escherichia coli O157-H7 str. Sakai	Obesumbacterium proteus	Pyrococcus horikoshii
Citrobacter cronae	Escherichia coli str. K-12 substr. MG1655	Pantoea agglomerans	Pyrococcus yayanosii
Citrobacter europaeus	Escherichia fergusonii	Pantoea allii	Rahnella aquatilis CIP 78.65 = ATCC 33071
Citrobacter farmeri	Escherichia marmotae	Pantoea ananatis PA13	Raoultella ornithinolytica
Citrobacter freundii	Escherichia ruysiae	Pantoea dispersa	Raoultella planticola
Citrobacter koseri ATCC BAA-895	Ewingella americana	Pantoea stewartii	Raoultella terrigena
Citrobacter portucalensis	Hafnia alvei	Pantoea vagans	Rosenbergiella epipactidis
Citrobacter werkmanii	Hafnia paralvei	Pectobacterium aroidearum	Rouxiella badensis
Citrobacter youngae	Homo sapiens	Pectobacterium atrosepticum	Saccharomyces cerevisiae
Cronobacter dublinensis subsp. dublinensis LMG 23823	Kalamiella piersonii	Pectobacterium brasiliense	Saccharolobus solfataricus
Cronobacter malonaticus LMG 23826	Klebsiella aerogenes	Pectobacterium carotovorum	Salmonella bongori N268-08
Cronobacter sakazakii	Klebsiella grimontii	Pectobacterium odoriferum	Salmonella enterica subsp. enterica serovar Typhimurium str. LT2
Cronobacter turicensis	Klebsiella michiganensis	Pectobacterium parmentieri	Serratia bockelmannii
Danio rerio	Klebsiella oxytoca	Pectobacterium polaris	Serratia entomophila
Dickeya dadantii 3937	Klebsiella pasteurii	Pectobacterium versatile	Serratia ficaria
Dickeya dianthicola	Klebsiella pneumoniae subsp. pneumoniae HS11286	Photorhabdus laumondii subsp. laumondii TTO1	Serratia fonticola
Dickeya fangzhongdai	Klebsiella quasipneumoniae	Plesiomonas shigelloides	Serratia grimesii
Dickeya solani	Klebsiella quasivariicola	Pluralibacter gergoviae	Serratia liquefaciens
Dickeya zeae	Thermoccoccus kodakarensis	Proteus faecis	Serratia marcescens
Drosophila melanogaster	Thermococcus barophilus MPT	Proteus mirabilis HI4320	Serratia nevei
Edwardsiella anguillarum ET080813	Thermococcus chitonophagus	Yersinia aldovae 670-83	Serratia plymuthica AS9
Edwardsiella ictaluri	Thermococcus gammatolerans	Yersinia aleksiciae	Serratia proteamaculans
Edwardsiella piscicida	Thermococcus litoralis	Yersinia alsatica	Serratia quinivorans
Edwardsiella tarda	Thermococcus onnurineus	Yersinia enterocolitica	Serratia rubidaea
Enterobacter asburiae	Thermococcus sibiricus	Yersinia frederiksenii ATCC 33641	Serratia ureilytica
Enterobacter bugandensis	Xenorhabdus bovienii str. feltiae Florida	Yersinia intermedia	Shigella boydii
Enterobacter cancerogenus	Yersinia kristensenii	Yersinia massiliensis CCUG 53443	Shigella dysenteriae
Enterobacter chengduensis	Yersinia mollaretii ATCC 43969	Yersinia pestis A1122	Shigella flexneri 2a str. 301
Enterobacter cloacae	Yersinia proxima	Yersinia pseudotuberculosis IP 32953	Shigella sonnei
Yersinia rochesterensis	Yersinia rohdei	Yersinia ruckeri	Yokenella regensburgei

Star History

Key Features

• CodonData
  CodonData facilitates preprocessing of genetic information by cleaning and translating DNA and protein sequences, handling FASTA files, and managing codon frequencies from databases like NCBI and Kazusa.

• CodonPrediction
  CodonPrediction enables preprocessing of sequences, the prediction of optimized DNA sequences tailored to specific organisms using the CodonTransformer model, and supports various other optimization strategies.

• CodonEvaluation
  CodonEvaluation provides tools to compute evaluation metrics such as Codon Similarity Index (CSI), GC content, and Codon Frequency Distribution, allowing for detailed assessment of optimized sequences.

• CodonUtils
  CodonUtils offers essential constants and helper functions for genetic sequence analysis, including amino acid mappings, codon tables, taxonomy ID management, and sequence validation.

• CodonJupyter
  CodonJupyter enhances Jupyter notebook workflows with interactive widgets for selecting organisms and inputting protein sequences, as well as formatting and displaying optimized DNA sequence outputs.
  
  

CodonData

The CodonData subpackage offers tools for preprocessing NCBI or Kazusa databases and managing codon-related data operations. It includes comprehensive functions for working with DNA sequences, protein sequences, and codon frequencies, providing a robust toolkit for sequence preprocessing and codon frequency analysis across different organisms.

Overview

This subpackage is suitable for:

• Preparing data for model training and inference
• Preprocessing and cleaning DNA and protein sequences
• Translating DNA sequences to protein sequences
• Reading and processing FASTA files
• Downloading and processing codon frequency data from the Kazusa database
• Calculating codon frequencies from given sequences
• Handling organism-specific codon tables and translations

Available Functions

• prepare_training_data(dataset: Union[str, pd.DataFrame], output_file: str, shuffle: bool = True) -> None

  Prepare a JSON dataset for training the CodonTransformer model. Process the input dataset, create the ‘codons’ column, handle organism IDs, and save the result to a JSON file.

• dataframe_to_json(df: pd.DataFrame, output_file: str, shuffle: bool = True) -> None

  Convert a pandas DataFrame to a JSON file format suitable for training CodonTransformer. Write each row of the DataFrame as a JSON object to the output file, with an option to shuffle the data.

• process_organism(organism: Union[str, int], organism_to_id: Dict[str, int]) -> int

  Process and validate the organism input, converting it to a valid organism ID. Handle both string (organism name) and integer (organism ID) inputs.

• get_codon_table(organism: str) -> int

  Return the appropriate NCBI codon table number for a given organism.

• preprocess_protein_sequence(protein: str) -> str

  Clean, standardize, and handle ambiguous amino acids in a protein sequence. Utilizes the ProteinConfig to handle ambiguous amino acids based on user-defined settings.

• replace_ambiguous_codons(dna: str) -> str

  Replace ambiguous codons in a DNA sequence with “UNK”.

• preprocess_dna_sequence(dna: str) -> str

  Clean and preprocess a DNA sequence by standardizing it and replacing ambiguous codons.

• get_merged_seq(protein: str, dna: str = "", separator: str = "_") -> str

  Merge protein and DNA sequences into a single string of tokens.

• is_correct_seq(dna: str, protein: str, stop_symbol: str = STOP_SYMBOL) -> bool

  Check if the given DNA and protein pair is correct based on specific criteria.

• get_amino_acid_sequence(dna: str, stop_symbol: str = "_", codon_table: int = 1, return_correct_seq: bool = True) -> Union[Tuple[str, bool], str]

  Translate a DNA sequence to a protein sequence using a specified codon table.

• read_fasta_file(input_file: str, output_path: str, organism: str = "", return_dataframe: bool = True, buffer_size: int = 50000) -> pd.DataFrame

  Read a FASTA file of DNA sequences and saves it to a Pandas DataFrame.

• download_codon_frequencies_from_kazusa(taxonomy_id: Optional[int] = None, organism: Optional[str] = None, taxonomy_reference: Optional[str] = None, return_original_format: bool = False) -> AMINO2CODON_TYPE

  Download and process codon frequency data from the Kazusa database for a given taxonomy ID or organism.

• build_amino2codon_skeleton(organism: str) -> AMINO2CODON_TYPE

  Create an empty skeleton of the amino2codon dictionary for a given organism.

• get_codon_frequencies(dna_sequences: List[str], protein_sequences: Optional[List[str]] = None, organism: Optional[str] = None) -> AMINO2CODON_TYPE

  Calculate codon frequencies based on a collection of DNA and protein sequences.

• get_organism_to_codon_frequencies(dataset: pd.DataFrame, organisms: List[str]) -> Dict[str, AMINO2CODON_TYPE]

  Generate a dictionary mapping each organism to its codon frequency distribution.
  
  

CodonPrediction

The CodonPrediction subpackage is an essential component of CodonTransformer, used for tokenizing input, loading models, predicting DNA sequences, and providing helper functions for data processing. It offers a comprehensive toolkit for working with the CodonTransformer model, covering tasks from model loading and configuration to various types of codon optimization and DNA sequence prediction.

Overview

This subpackage contains functions and classes that handle the core prediction functionality of CodonTransformer. It includes tools for working with the BigBird transformer model, tokenization, and various codon optimization strategies.

Available Functions and Classes

• predict_dna_sequence(protein: str, organism: Union[int, str], device: torch.device, tokenizer: Union[str, PreTrainedTokenizerFast], model: Union[str, torch.nn.Module], attention_type: str = "original_full", deterministic: bool = True, temperature: float = 0.2, top_p: float = 0.95, num_sequences: int = 1, match_protein: bool = False) -> DNASequencePrediction

  Predict the DNA sequence for a given protein using the CodonTransformer model.

• sample_non_deterministic(logits: torch.Tensor, temperature: float = 0.2, top_p: float = 0.95) -> List[int]

  Sample token indices from logits using temperature scaling and nucleus (top-p) sampling.

• load_model(path: str, device: torch.device = None, num_organisms: int = None, remove_prefix: bool = True, attention_type: str = "original_full") -> torch.nn.Module

  Load a BigBirdForMaskedLM model from a file or checkpoint.

• load_bigbird_config(num_organisms: int) -> BigBirdConfig

  Load the configuration object used to train the BigBird transformer.

• create_model_from_checkpoint(checkpoint_dir: str, output_model_dir: str, num_organisms: int) -> None

  Save a model to disk using a previous checkpoint.

• load_tokenizer(tokenizer_path: str) -> PreTrainedTokenizerFast

  Create and return a tokenizer object from the given tokenizer path.

• tokenize(batch: List[Dict[str, Any]], tokenizer_path: str = "", tokenizer_object: Optional[PreTrainedTokenizerFast] = None, max_len: int = 2048) -> BatchEncoding

  Tokenize sequences given a batch of input data.

• validate_and_convert_organism(organism: Union[int, str]) -> Tuple[int, str]

  Validate and convert the organism input to both ID and name.

• get_high_frequency_choice_sequence(protein: str, codon_frequencies: Dict[str, Tuple[List[str], List[float]]]) -> str

  Return a DNA sequence optimized using the High Frequency Choice (HFC) approach.

• precompute_most_frequent_codons(codon_frequencies: Dict[str, Tuple[List[str], List[float]]]) -> Dict[str, str]

  Precompute the most frequent codon for each amino acid.

• get_high_frequency_choice_sequence_optimized(protein: str, codon_frequencies: Dict[str, Tuple[List[str], List[float]]]) -> str

  An efficient implementation of the HFC approach, up to 10 times faster than the original.

• get_background_frequency_choice_sequence(protein: str, codon_frequencies: Dict[str, Tuple[List[str], List[float]]]) -> str

  Return a DNA sequence optimized using the Background Frequency Choice (BFC) approach.

• precompute_cdf(codon_frequencies: Dict[str, Tuple[List[str], List[float]]]) -> Dict[str, Tuple[List[str], Any]]

  Precompute the cumulative distribution function (CDF) for each amino acid.

• get_background_frequency_choice_sequence_optimized(protein: str, codon_frequencies: Dict[str, Tuple[List[str], List[float]]]) -> str

  An efficient implementation of the BFC approach, up to 8 times faster than the original.

• get_uniform_random_choice_sequence(protein: str, codon_frequencies: Dict[str, Tuple[List[str], List[float]]]) -> str

  Return a DNA sequence optimized using the Uniform Random Choice (URC) approach.

• get_icor_prediction(input_seq: str, model_path: str, stop_symbol: str) -> str

  Return an optimized codon sequence for the given protein sequence using ICOR (Improving Codon Optimization with Recurrent Neural Networks).
  
  

CodonEvaluation

The CodonEvaluation subpackage offers functions for calculating evaluation metrics related to codon usage and DNA sequence analysis, used for assessing the quality and characteristics of DNA sequences, especially in codon optimization. It provides a comprehensive toolkit for evaluating DNA sequences and codon usage, performingng genetic data analysis within the CodonTransformer package.

Overview

The CodonEvaluation module includes functions to compute metrics such as Codon Adaptation Index (CAI)/Codon Similarity Index (CSI) weights, GC content, codon frequency distribution (CFD), %MinMax, sequence complexity, and sequence similarity. These metrics are valuable for analyzing and comparing DNA sequences across different organisms.

Available Functions

• get_organism_to_CAI_weights(dataset: pd.DataFrame, organisms: List[str]) -> Dict[str, dict]

  Calculate the Codon Adaptation Index (CAI) weights for a list of organisms.

• get_GC_content(dna: str, lower: bool = False) -> float

  Compute the GC content of a DNA sequence.

• get_cfd(dna: str, codon_frequencies: Dict[str, Tuple[List[str], List[float]]], threshold: float = 0.3) -> float

  Calculate the codon frequency distribution (CFD) metric for a DNA sequence.

• get_min_max_percentage(dna: str, codon_frequencies: Dict[str, Tuple[List[str], List[float]]], window_size: int = 18) -> List[float]

  Calculate the %MinMax metric for a DNA sequence.

• get_sequence_complexity(dna: str) -> float

  Compute the sequence complexity score of a DNA sequence.

• get_sequence_similarity(original: str, predicted: str, truncate: bool = True, window_length: int = 1) -> float

  Calculate the sequence similarity between two sequences.
  
  

CodonUtils

The CodonUtils subpackage contains constants and helper functions essential for working with genetic sequences, amino acids, and organism data in the CodonTransformer package. It provides tools for genetic sequence analysis, organism identification, and data processing, forming the foundation for many core functionalities within the CodonTransformer package.

Contents

Constants

• AMINO_ACIDS: List of all standard amino acids
• STOP_SYMBOLS: List of possible stop symbols to end the protein with
• AMBIGUOUS_AMINOACID_MAP: Mapping of ambiguous amino acids to standard amino acids
• START_CODONS and STOP_CODONS: Lists of start and stop codons
• TOKEN2INDEX and INDEX2TOKEN: Mappings between tokens and their indices
• AMINO_ACID_TO_INDEX: Dictionary mapping each amino acid and stop symbol to indices of codon tokens that translate to it
• TOKEN2MASK: Mapping for mask tokens
• FINE_TUNE_ORGANISMS: List of organisms used for fine-tuning
• ORGANISM2ID: Dictionary mapping organisms to their respective IDs
• NUM_ORGANISMS, MAX_LEN, MAX_AMINO_ACIDS, STOP_SYMBOL: Various constants for sequence processing

Classes

• DNASequencePrediction

  Dataclass for holding DNA sequence prediction outputs.

• IterableData

  Base class for iterable datasets in parallel multi-processing environments.

• IterableJSONData

  Class for iterating over lines of a JSON file.

• ConfigManager

  An abstract base class for managing configuration settings.

• ProteinConfig:

  A singleton class derived from ConfigManager for managing protein-specific configurations. It allows customization of ambiguous amino acid handling.

Functions

• load_python_object_from_disk(file_path: str) -> Any

  Load a Pickle object from disk.

• save_python_object_to_disk(input_object: Any, file_path: str) -> None

  Save a Python object to disk using Pickle.

• find_pattern_in_fasta(keyword: str, text: str) -> List[str]

  Find a specific keyword pattern in text (useful for FASTA sequences).

• get_organism2id_dict(organism_reference: str) -> Dict[str, int]

  Get a dictionary mapping organisms to their indices.

• get_taxonomy_id(taxonomy_reference: str, organism: str, return_dict: bool = False) -> Union[int, Dict[str, int]]

  Get taxonomy ID for an organism or return the entire mapping.

• sort_amino2codon_skeleton(amino2codon: Dict[str, List[str]]) -> Dict[str, List[str]]

  Sort the amino2codon dictionary alphabetically.

• load_pkl_from_url(url: str) -> Any

  Download and load a Pickle file from a URL.
  
  

CodonJupyter

The CodonJupyter subpackage offers Jupyter-specific functions for displaying interactive widgets, facilitating user interaction with the CodonTransformer package in a Jupyter notebook environment. It improves the user experience by providing interactive and visually appealing interfaces for input and output.

Overview

This subpackage can be used for:

• Creating and displaying interactive widgets for organism selection and protein sequence input
• Handling user inputs and storing them in a container
• Formatting and displaying the model output in a visually appealing manner

Classes and Functions

• UserContainer

  A container class to store user inputs for organism and protein sequence.

  Attributes:

  • organism (int): The selected organism ID
  • protein (str): The input protein sequence

• display_organism_dropdown(organism2id: Dict[str, int], container: UserContainer) -> None

  Display a dropdown widget for selecting an organism from a list and updates the organism ID in the provided container.

• display_protein_input(container: UserContainer) -> None

  Display a widget for entering a protein sequence and saves the entered sequence to the container.

• format_model_output(output: DNASequencePrediction) -> str

  Format the DNA sequence prediction output in a visually appealing and easy-to-read manner. Take a DNASequencePrediction object and return a formatted string.

Usage

Checkout our Google Colab Notebook for an example use case!

Contribution

We welcome contributions to CodonTransformer! Please fork the repository and submit a pull request. For major changes, please open an issue first to discuss what you would like to change.

Citation

If you use CodonTransformer or our data in your research, please cite our work:

@article{Fallahpour_Gureghian_Filion_Lindner_Pandi_2025,
  title={CodonTransformer: a multispecies codon optimizer using context-aware neural networks},
  volume={16},
  ISSN={2041-1723},
  url={https://www.nature.com/articles/s41467-025-58588-7},
  DOI={10.1038/s41467-025-58588-7},
  number={1},
  journal={Nature Communications},
  author={Fallahpour, Adibvafa and Gureghian, Vincent and Filion, Guillaume J. and Lindner, Ariel B. and Pandi, Amir},
  year={2025},
  month=apr,
  pages={3205},
  language={en}
}