AntPack is a toolkit for antibody numbering, data processing, statistical inference and machine learning for antibody sequences. It is currently in active development -- more updates soon! For installation and how to use, see the docs.
Starting in version 0.2.0, there are only two dependencies, numpy and pybind. We've also simplified the SingleChainAnnotator API slightly (this does cause a possible breaking change). We've also introduced a tool for extracting the variable heavy and light regions from a sequence that may contain both, a tool for detecting common liabilities in antibody variable region sequences (N-glycosylation motifs, deamidation motifs, etc.), and a tool for identifying the human V or J gene most similar to an input sequence.
Numbering antibody sequences is an important precursor for many statistical inference / machine learning applications. AntPack is orders of magnitude faster for numbering antibody sequences than existing tools in the literature (e.g. ANARCI, AbRSA), while providing >= reliability.
Identifying the most similar human V / J gene sequences is useful for a variety of purposes. AntPack provides tools for determining which human V and J gene sequences are most similar to the variable region chain provided as input.
Minimizing the risk of immunogenicity is important for selecting clinical candidates. In AntPack v0.1.0, we introduce a simple, fully interpretable generative model for human heavy and light chains that outperforms all comparators in the literature on a large held-out test set for distinguishing human sequences from those of other species. This scoring tool can be used to score sequences for humanness, suggest modifications to make them more human, identify liabilities, and generate highly human sequences that contain selected motifs.
Some sequence motifs are known to be associated with developability issues -- certain motifs are known, for example, to be prone to N-glycosylation or deamidation. AntPack provides a tool for finding these "liability" motifs in an input sequence. Note that that identifying liabilities through finding motifs in this way is known to be prone to false positives (an N-glycosylation motif, for example, will not always be glycosylated). Still, these kinds of alerts can be useful for making yourself aware of potential developability issues.
If using AntPack in research intended for publication, please cite either the preprint:
Jonathan Parkinson and Wei Wang. 2024. For antibody sequence generative modeling, mixture models may be all you need. bioRxiv: https://doi.org/10.1101/2024.01.27.577555
or the final paper in Bioinformatics.