LAUSR

Minimizers are widely used to sample representative k-mers from biological sequences in many applications, such as read mapping and taxonomy prediction. In most scenarios, having the minimizer scheme select as few k-mer positions as possible (i.e., having a low density) is desirable to reduce computation and memory cost. Despite the growing interest in minimizers, learning an effective scheme with optimal density is still an open question, as it requires solving an apparently challenging discrete optimization problem on the permutation space of k-mer orderings. Most existing schemes are designed to work well in expectation over random sequences, which have limited applicability to many practical tools. On the other hand, several methods have been proposed to construct minimizer schemes for a specific target sequence. These methods, however, only approximate the original objective with likewise discrete surrogate tasks that are not able to significantly improve the density performance. This article introduces the first continuous relaxation of the density minimizing objective, DeepMinimizer, which employs a novel Deep Learning twin architecture to simultaneously ensure both validity and performance of the minimizer scheme. Our surrogate objective is fully differentiable and, therefore, amenable to efficient gradient-based optimization using GPU computing. Finally, we demonstrate that DeepMinimizer discovers minimizer schemes that significantly outperform state-of-the-art constructions on human genomic sequences.