build(deps): bump biopython from 1.81 to 1.82

[dependabot]

Bumps biopython from 1.81 to 1.82.

Changelog

Sourced from biopython's changelog.

22 December 2023: Biopython 1.82

This release of Biopython supports Python 3.8, 3.9, 3.10, 3.11 and 3.12. It has also been tested on PyPy3.8 v7.8.16.

The inplace argument of complement and reverse_complement in Bio.Seq now always default to False both for Seq and MutableSeq objects. To modify a MutableSeq in-place, use inplace=True.

A new class CodonAligner was added to Bio.Align. A CodonAligner object can align a nucleotide sequence to the amino acid sequence it encodes, using a dynamic programming algorithm modeled on PairwiseAligner to take frame shifts into account. The CodonAligner returns Alignment objects. By calling the new mapall method on an Alignment object storing a multiple sequence alignment of amino acid sequences, with nucleotide-to-amino acid alignments generated by CodonAligner as the argument, a codon-by-codon multiple sequence alignment of nucleotide sequences can be obtained. The new submodule Bio.Align.analysis provides functions to estimate synonymous and nonsynonymous mutations and to perform the McDonald-Kreitman test on the codon multiple sequence alignments. Together, this provides the same functionality as the Bio.codonalign module, but uses the standard Alignment class, and does not rely on regular expression searching to align a nucleotide sequence to an amino acid sequence.

The hmmer3-text SearchIO format now also extracts the similarity string of the parsed alignments. This value is available under the 'similarity' key of the aln_annotation attribute of each HSP, the same as how it is done in other SearchIO formats.

HMMER results with the full path to the hmmer executable in the banner are now parsed correctly. This should help Windows users and users with python installations in non-default locations.

We now have basic type hint annotations in various modules including Seq, SeqRecord, and SeqIO. This should help anyone using an editor or IDE with type-aware autocomplete, or in conjunction with mypy as a pre-commit check this can catch passing the wrong types to Biopython functions/methods.

Calling iter on a PairwiseAlignments object returned by a PairwiseAigner previously reset the iterator such that it will start from the first alignment when iterating. As a side effect, this will cause all other iterators of the alignments to reset as well, which is bug prone. Instead, calling iter on a PairwiseAlignments object will now return itself. The iterator can be reset by calling the rewind method.

Calling secondary_structure_fraction() on a ProtParam.ProteinAnalysis object historically returned (sheet, turn, helix) while claiming to return (helix, turn, sheet). This was fixed to correctly return (helix, turn, sheet). Additionally, the amino acids considered were revised as per recent literature.

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