- Introduce new `obipackage` library with pipeline stages, scheduler and worker pool - Refactor path expansion in `obiread`: replace old list_of_files with new PathIter iterator - Add MIME type detection using `infer` crate (fastq/fasta) - Update dependencies in Cargo.lock: add bumpalo, byteorder, cfb (with deps), fnv, infer, js-sys/uuid/wasm-bindgen ecosystem - Fix formatting and improve tests in SuperKmer (canonical, revcomp) * Note: edition = "2024" in obipipeline/Cargo.toml is invalid; should be 2021
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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 k−1 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), with the constraint that non-degenerate m-mers are always preferred over degenerate ones. A degenerate m-mer is one composed of a single repeated nucleotide (all-A, all-C, all-G, or all-T); such m-mers are selected only if no non-degenerate candidate exists in the window.
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/(k−m+2) [@Zheng2020-ji; @Golan2025-xf], so the expected number of consecutive k-mers per super-kmer is (k−m+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
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The expected length formula and the density approximation 2/(k−m+2) should be verified against the values reported in [@Zheng2020-ji] and [@Golan2025-xf]. ↩︎