Mercurial > repos > cpt > cpt_linear_genome_plot
view dna_features_viewer/biotools.py @ 1:e923c686ead9 draft
planemo upload commit 94b0cd1fff0826c6db3e7dc0c91c0c5a8be8bb0c
author | cpt |
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date | Mon, 05 Jun 2023 02:45:31 +0000 |
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children | b79e98299a78 |
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import textwrap from Bio.Seq import Seq from Bio.SeqFeature import SeqFeature, FeatureLocation from Bio.PDB.Polypeptide import aa1, aa3 from Bio import SeqIO try: from BCBio import GFF except ImportError: class GFF: def parse(*a): """Not available. Please install bcbio-gff.""" raise ImportError("Please install the bcbio-gff library to parse GFF data") def complement(dna_sequence): """Return the complement of the DNA sequence. For instance ``complement("ATGCCG")`` returns ``"TACGGC"``. Uses BioPython for speed. """ return str(Seq(dna_sequence).complement()) def reverse_complement(sequence): """Return the reverse-complement of the DNA sequence. For instance ``complement("ATGCCG")`` returns ``"GCCGTA"``. Uses BioPython for speed. """ return complement(sequence)[::-1] aa_short_to_long_form_dict = { _aa1: _aa3[0] + _aa3[1:].lower() for (_aa1, _aa3) in zip(aa1 + "*", aa3 + ["*"]) } def translate(dna_sequence, long_form=False): """Translate the DNA sequence into an amino-acids sequence MLKYQT... If long_form is true, a list of 3-letter amino acid representations is returned instead (['Ala', 'Ser', ...]). """ result = str(Seq(dna_sequence).translate()) if long_form: result = [aa_short_to_long_form_dict[aa] for aa in result] return result def extract_graphical_translation(sequence, location, long_form=False): """Return a string of the "graphical" translation of a sequence's subsegment. Here "graphical" means that the amino acid sequence is always given left-to-right, as it will appear under the sequence in the plot. This matters when the location is on the -1 strand. In this case, the amino-acids are determined by (part of) the reverse-complement of the sequence, however the sequence returned will be the mirror of the translated sequence, as this is the left-to-right order in which the codons corresponding to the amino-acids appear in the sequence. Parameters ---------- sequence An "ATGC" string. location Either (start, end) or (start, end, strand), with strand in (0, 1, -1). long_form if True, a list of 3-letter amino acid representations is returned instead (['Ala', 'Ser', ...]). """ if len(location) == 3: start, end, strand = location else: start, end = location strand = 1 subsequence = sequence[start:end] if strand == -1: subsequence = reverse_complement(subsequence) translation = translate(subsequence, long_form=long_form) if strand == -1: translation = translation[::-1] return translation def load_record(path): """Load a Genbank file""" if isinstance(path, str): # Input is a file path if path.lower().endswith(".gff"): return list(GFF.parse(path))[0] else: return SeqIO.read(path, "genbank") else: # Input is a file-like object try: return SeqIO.read(path, "genbank") except: path.seek(0) return list(GFF.parse(path))[0] def annotate_biopython_record( seqrecord, location="full", feature_type="misc_feature", margin=0, **qualifiers ): """Add a feature to a Biopython SeqRecord. Parameters ---------- seqrecord The biopython seqrecord to be annotated. location Either (start, end) or (start, end, strand). (strand defaults to +1) feature_type The type associated with the feature margin Number of extra bases added on each side of the given location. qualifiers Dictionnary that will be the Biopython feature's `qualifiers` attribute. """ if location == "full": location = (margin, len(seqrecord) - margin) strand = location[2] if len(location) == 3 else 1 seqrecord.features.append( SeqFeature( FeatureLocation(location[0], location[1], strand), qualifiers=qualifiers, type=feature_type, ) ) def find_narrowest_text_wrap(text, max_line_length): """Wrap the text into a multi-line text minimizing the longest line length. This is done by first wrapping the text using max_line_length, then attempt new wraps by iteratively decreasing the line_length, as long as the number of lines stays the same as with max_line_length. """ narrowest_wrap = textwrap.wrap(text, max_line_length) narrowest_width = max([len(l) for l in narrowest_wrap]) for line_length in range(max_line_length - 1, 0, -1): wrap = textwrap.wrap(text, line_length) if len(wrap) <= len(narrowest_wrap): width = max([len(l) for l in wrap]) if width < narrowest_width: narrowest_wrap = wrap narrowest_width = width else: break return "\n".join(narrowest_wrap)