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68 lines
3.0 KiB
Python
68 lines
3.0 KiB
Python
'''
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#Author, date: Godwin Ani and Laura Katz, 9th- Feb - 2023.
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#Dependencies: Python3, CD-Hit
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#Intent: For clustering nucleotide or amino acid sequences with the CD-Hit program.
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#Inputs: A folder of containing Amino acid or DNA fasta files.
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#Outputs: A folder of clustered files.
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#Example: python Cluster_v2.0.py --type dna --identity 0.95 --overlap 0.67 --input input_folder_dna --output output_folder_dna
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'''
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import os
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import argparse
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from tqdm import tqdm
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import subprocess
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def input_validation(value, error_message):
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try:
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integer, fractional = value.split('.')
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value = float(value)
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if int(integer) == 0 and len(fractional) == 2:
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return value
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except ValueError:
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pass
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print(error_message)
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exit(1)
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def cluster_sequences(program, identity, overlap, input_folder, output_folder):
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for file in tqdm(os.listdir(input_folder)):
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if file.endswith('.fasta'):
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subprocess.run([f'{program}', '-i', f'{input_folder}/{file}', '-o', f'{output_folder}/{file}', '-c', f'{identity}', '-d', '0', '-aS', f'{overlap}'])
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for file in os.listdir(output_folder):
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if file.endswith('.clstr'):
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os.rename(f'{output_folder}/{file}', f'{output_folder}/{file.split("FILE")[0]}Clustered.txt')
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def main():
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parser = argparse.ArgumentParser(description='Cluster amino acid or DNA sequences using CD-HIT.')
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parser.add_argument('--type', choices=['aa', 'dna'], required=True, help='Type of sequences (aa for Amino Acids, dna for DNA)')
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parser.add_argument('--identity', type=str, required=True, help='Sequence Identity Threshold (e.g., 0.99, 0.95)')
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parser.add_argument('--overlap', type=str, required=True, help='Sequence Alignment Overlap Value (e.g., 0.67, 0.75)')
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parser.add_argument('--input', type=str, required=True, help='Input folder containing sequences in fasta format')
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parser.add_argument('--output', type=str, required=True, help='Output folder for clustered sequences')
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args = parser.parse_args()
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if not os.path.isdir(args.input):
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print(f'Error: Input folder "{args.input}" does not exist.')
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exit(1)
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if not os.path.isdir(args.output):
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os.mkdir(args.output)
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if args.type == 'aa':
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identity = input_validation(args.identity, 'ERROR! Use format 0.## for Amino acids sequence identity threshold.')
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overlap = input_validation(args.overlap, 'ERROR! Use format 0.## for Amino acids sequence alignment overlap value.')
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cluster_sequences('cd-hit', identity, overlap, args.input, args.output)
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elif args.type == 'dna':
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identity = input_validation(args.identity, 'ERROR! Use format 0.## for DNA sequence identity threshold.')
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overlap = input_validation(args.overlap, 'ERROR! Use format 0.## for DNA sequence alignment overlap value.')
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cluster_sequences('cd-hit-est', identity, overlap, args.input, args.output)
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else:
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print('Invalid sequence type. Choose "aa" for Amino Acids or "dna" for DNA.')
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exit(1)
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if __name__ == "__main__":
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main()
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