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Kmers and super-kmers

Kmers

A kmer is a DNA subsequence of fixed length k. Two constraints govern the choice of k:

  • k ∈ [11, 31]: the range ensures the kmer is long enough to be specific and short enough to fit in a single machine word.
  • k is odd: an odd-length sequence cannot equal its own reverse complement (no palindromes). This guarantees that the canonical form min(kmer, revcomp(kmer)) is always strictly defined — the two orientations are always distinct — which is required for strand-independent counting.

Super-kmers

A super-kmer is a maximal run of consecutive kmers from a DNA read, each overlapping the next by k1 nucleotides. Each kmer of the run carries the same canonical minimizer. The canonical minimizer of a kmer is the smallest value of min(m-mer, revcomp(m-mer)) over all m-mers within the kmer (m < k, m odd).

Canonical super-kmers

A canonical super-kmer is the lexicographic minimum of a super-kmer and its reverse complement:

canonical(super-kmer) = min(super-kmer, revcomp(super-kmer))

When a read and its reverse-complement are both sequenced, they produce super-kmers that are reverse complements of each other. Both map to the same canonical form: the same genomic region is represented by a single canonical super-kmer regardless of which strand was read.

Expected length of a super-kmer

For a random minimizer of length m over k-mers of length k, the density of minimizer positions is approximately 2/(km+2) [@Zheng2020-ji; @Golan2025-xf], so the expected number of consecutive k-mers per super-kmer is (km+2)/2. A run of n k-mers spans n + k 1 nucleotides, giving:

L_{\text{nt}} = \frac{k-m+2}{2} + k - 1

For k=31, m=13: expected ≈ 40 nt. In practice super-kmers rarely exceed a few dozen nucleotides.1


  1. The expected length formula and the density approximation 2/(km+2) should be verified against the values reported in [@Zheng2020-ji] and [@Golan2025-xf]. ↩︎