Syncmers are more sensitive than minimizers for selecting conserved k-mers in biological sequences

Abstract

Minimizers are widely used to select subsets of fixed-length substrings (k-mers) from biological sequences in applications ranging from read mapping to taxonomy prediction and indexing of large datasets. The minimizer of a string of w consecutive k-mers is the k-mer with smallest value according to an ordering of all k-mers. Syncmers are a family of alternative methods which select k-mers by inspecting the position of the smallest-valued substring of length s<k within the k-mer. For example, a closed syncmer selected if its smallest s-mer is at the start of end of the k-mer. At least one closed syncmer must be found in every window of length (k - s) k-mers. Unlike a minimizer, a syncmer is identified by its sequence alone, and is therefore synchronized in the following sense: if a given k-mer is selected from one sequence, it will also be selected from any other sequence. Also, minimizers can be deleted by mutations in flanking sequence, which cannot happen with syncmers. Experiments on minimizers with parameters used in the minimap2 read mapper and Kraken taxonomy prediction algorithm respectively show that syncmers can simultaneously achieve both lower density and higher conservation compared to minimizers.