A new attribution metric for autoregressive generative sequence models, GAMA, recovers implanted motifs in synthetic data and partially identifies known antibody binding positions.
A bagging SVM to learn from positive and unlabeled examples
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abstract
We consider the problem of learning a binary classifier from a training set of positive and unlabeled examples, both in the inductive and in the transductive setting. This problem, often referred to as \emph{PU learning}, differs from the standard supervised classification problem by the lack of negative examples in the training set. It corresponds to an ubiquitous situation in many applications such as information retrieval or gene ranking, when we have identified a set of data of interest sharing a particular property, and we wish to automatically retrieve additional data sharing the same property among a large and easily available pool of unlabeled data. We propose a conceptually simple method, akin to bagging, to approach both inductive and transductive PU learning problems, by converting them into series of supervised binary classification problems discriminating the known positive examples from random subsamples of the unlabeled set. We empirically demonstrate the relevance of the method on simulated and real data, where it performs at least as well as existing methods while being faster.
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cs.LG 1years
2025 1verdicts
CONDITIONAL 1representative citing papers
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Attribution assignment for deep-generative sequence models enables interpretability analysis using positive-only data
A new attribution metric for autoregressive generative sequence models, GAMA, recovers implanted motifs in synthetic data and partially identifies known antibody binding positions.