Barely Significant
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DESMAN: a new tool for de novo extraction of strains from metagenomes.

Genome Biol · 2017 · PMC5607848 · PMID 28934976

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0.0600
closest p · 1.2× alpha
0.0600
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almost significantp -value = 0.06so close (0.05 < p ≤ 0.1)
The median and mean SCG SNV error rates for the inferred haplotypes in a cluster were also higher at 0.641% and 3.583%, respectively, compared to 0.25% and 2.38% for DESMAN, an increase that was almost significant, when we compared the Lineage and DESMAN error rates across clusters (Kruskal–Wallis paired ANOVA, p -value = 0.06).

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