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Andrei Slabodkin

Researcher at University of Oslo

Publications -  10
Citations -  231

Andrei Slabodkin is an academic researcher from University of Oslo. The author has contributed to research in topics: Paratope & Epitope. The author has an hindex of 4, co-authored 9 publications receiving 66 citations. Previous affiliations of Andrei Slabodkin include Oslo University Hospital.

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A compact vocabulary of paratope-epitope interactions enables predictability of antibody-antigen binding.

TL;DR: In this paper, the authors identify structural interaction motifs, which together compose a commonly shared structure-based vocabulary of paratope-epitope interactions, and show that this vocabulary enables the machine learnability of antibody-antigen binding using generative machine learning.
Posted ContentDOI

A compact vocabulary of paratope-epitope interactions enables predictability of antibody-antigen binding

TL;DR: The largest available set of non-redundant antibody-antigen structures are screened for binding patterns and identified structural interaction motifs are identified, which together compose a vocabulary of paratope-epitope interactions that is universally shared among investigated antibody-antsigen structures.
Journal ArticleDOI

The immuneML ecosystem for machine learning analysis of adaptive immune receptor repertoires

TL;DR: In this article, the authors present an open-source collaborative ecosystem for machine learning analysis of adaptive immune receptor repertoires (AIRR) and demonstrate the broad applicability of immuneML by reproducing a large-scale study on immune state prediction, developing, integrating and applying a novel deep learning method for antigen specificity prediction and showcasing streamlined interpretability-focused benchmarking of AIRR ML.
Posted ContentDOI

Individualized VDJ recombination predisposes the available Ig sequence space

TL;DR: In this article, a sensitivity-tested distance measure was devised to enable inter-individual comparison of VDJ recombination models, and it was shown that population-wide individualized recombination can result in orders of magnitude of difference in the probability to generate (auto)antigen-specific Ig sequences.