Genomic sequence alignment uses BLOSUM substitution matrices and dynamic programming -- expensive, heuristic, patented. CRT approach: encode each codon as a ring element in Z/12612600. The 6 CRT channels naturally separate: positions 1-3 map to D,K,E channels, amino acid identity to b channel, wobble degeneracy to L, GC content to G. Alignment = coupling distance. Synonymous mutations = small CRT distance (b channel preserved). The genetic code IS a CRT code.
How It Works
CRT Genetic Code Theorem
The standard genetic code maps 64 codons to 20 amino acids + stop. This degeneracy (wobble) is CRT error tolerance: synonymous codons differ only in the E channel (position 3) while the b channel (AA identity, mod 49) is preserved. CRT distance between sequences = sum of per-channel circular distances. Synonymous mutations have near-zero b-channel distance. Non-synonymous mutations create large b-channel jumps. L=11 = wobble class detector. The 490 split: DEAD={D,E,b} = genetic data, ALIVE={K,L,G} = validation channels.
64 codons
Ring elements
Each codon = one number in Z/12612600. 6 channels = 6 genetic properties.
Wobble = ECC
L=11 tolerance
Synonymous substitutions change E channel only. b channel (AA) preserved.
Coupling = distance
Evolutionary metric
CRT distance between codons = functional distance. Silent mutations are algebraically close.
No BLOSUM
No matrix
Substitution scoring from ring structure, not empirical log-odds matrices.
Align Sequences
Compare to reference (1-3):
Aligns variant against reference HBB sequence. Shows codon-by-codon CRT decomposition, synonymous vs non-synonymous classification, coupling distance.