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Full reimplementation of DnaSP 6 for population genetics analysis of aligned DNA sequences. Covers nucleotide diversity, haplotype statistics, neutrality tests (Tajima's D, Fu & Li's D*/F*, R2), linkage disequilibrium (D, D', R², ZnS, Za, ZZ), minimum recombination (Rm), mismatch distribution, InDel polymorphism, between-population divergence (Dxy, Da, fixed/shared sites), outgroup-based Fu & Li D/F tests (fuliout), the HKA multi-locus neutrality test (hka), the McDonald-Kreitman test (mk), Ka/K
Passed 17 of 20 test cases with the skill, and 3 of 20 without it.
and 18 more in the full report
16 fixed3 passed either way3 still failing1 broke
Tokens, turns and time describe resource use, not a dollar price.
One of 16 test cases the skill fixed. Same model, same prompt, with and without the skill.
Which InDel polymorphism model is implemented for analyzing deletion/insertion variation in sequence alignments?
| Checked | Without skill | With skill |
|---|---|---|
| Identifies the InDel analysis as DnaSP Model 1 diallelic diversity. | Missed | Passed |
The instructions your model reads when the skill loads.
Fire when a user requests population-genetic analysis of aligned DNA, a supported VCF, or a DnaSP-compatible statistic listed below. Do NOT fire for sequence alignment, read mapping, haplotype phasing, clinical advice or unsupported coalescent significance tests.
Analyse genetic variation in supplied alignments using 16 selected DnaSP methods. This is not a complete replacement for the DnaSP GUI or all its analysis modes. Read the statistical reference for definitions, exclusions, source conventions, file formats, examples and release validation evidence.
Fu and Li D*/F* and outgroup D/F mirror Data > Segregating Sites/Mutations = Segregating sites, using DnaSP's v5-style panels. The rp49 Eta-setting D*/F* figures can be reproduced by substituting eta for S, but this is not a general
test cases passed, vs 3 / 20 without
More skills from the same source and nearby in the registry, with their headline benchmark lift.