| Hypotheses | ||||||
| ID | Tier | Claim | Status | Layers | Species | Depends on |
|---|---|---|---|---|---|---|
| H01 | 1 | Colony identity explains more gene-expression variance than season in all three species | not supported | genes | Apul, Peve, Ptuh | |
| H02 | 1 | Transcriptional plasticity across the year ranks Acropora > Pocillopora > Porites | supported | genes | Apul, Peve, Ptuh | H01 |
| H03 | 1 | Seasonal expression responses are conserved across the three species at orthologous genes | not supported | genes | Apul, Peve, Ptuh | H02 |
| H04 | 2 | DNA methylation is more stable within colonies over time than gene expression | inconclusive | cpg, genes | Apul, Peve, Ptuh | H01 |
| H05 | 2 | Gene-body methylation is positively associated with expression level and negatively with its temporal variability | supported | cpg, genes, annotation | Apul, Peve, Ptuh | H04 |
| H06 | 2 | Seasonal change in gene-body methylation tracks seasonal change in expression at the same genes | inconclusive | cpg, genes, annotation | Apul, Peve, Ptuh | H04, H05 |
| H07 | 2 | Seasonal miRNA expression profiles are conserved across species for shared miRNA families | inconclusive | mirna | Apul, Peve, Ptuh | |
| H08 | 2 | lncRNA-mRNA co-expression at a fixed correlation threshold exceeds a permutation null | supported | lncrna, genes | Apul, Peve, Ptuh | |
| H15 | 2 | Seasonal gene-body methylation changes persist after temperature reverses, while expression changes revert | inconclusive | cpg, genes, temperature, annotation | Apul, Peve, Ptuh | H04, H05, H06 |
| H16 | 2 | Expression change precedes gene-body methylation change, not the reverse | not supported | cpg, genes, annotation, physiology | Apul, Peve, Ptuh | H05, H06 |
| H17 | 2 | lncRNAs co-vary with neighboring protein-coding genes more than with expression-matched distant genes, decaying with distance | supported | lncrna, genes, annotation | Apul, Peve, Ptuh | H08 |
| H23 | 2 | Acropora's excess seasonal expression plasticity is concentrated in low-methylation orthologs | inconclusive | cpg, genes, annotation | Apul, Peve, Ptuh | H02, H05 |
| H24 | 2 | Orthologs retain similar gene-body methylation ranks across species | inconclusive | cpg, genes, annotation | Apul, Peve, Ptuh | H05 |
| H25 | 2 | Beyond 2 kb, local co-expression is practically equivalent for lncRNA–gene and gene–gene pairs | inconclusive | lncrna, genes, annotation | Apul, Peve, Ptuh | H08, H17 |
| H26 | 2 | Distal lncRNA–mRNA co-expression predicts gene expression in held-out colonies | not supported | lncrna, genes, annotation | Apul, Peve, Ptuh | H08, H17 |
| H09 | 3 | Symbiont density and chlorophyll predict host gene-expression modules | not supported | genes, physiology | Apul, Peve, Ptuh | H01 |
| H10 | 3 | Symbiodiniaceae ITS2 community composition is fixed by colony and does not shift seasonally | supported | its2, physiology | Apul, Peve, Ptuh | |
| H11 | 3 | Cumulative thermal exposure before sampling predicts expression of heat-stress orthologs | withdrawn | genes, temperature | Apul, Peve, Ptuh | H03 |
| H12 | 3 | Site nutrient context modulates the seasonal trajectory of host physiology | inconclusive | physiology | Apul, Peve, Ptuh | |
| H20 | 3 | Colonies whose transcriptome lags current temperature lose biomass and calcification by the next timepoint | withdrawn | genes, temperature, physiology | Apul, Peve, Ptuh | H02, H11 |
| H21 | 3 | Colonies with higher constitutive stress-gene expression show smaller seasonal responses in those genes | inconclusive | genes | Apul, Peve, Ptuh | H02, H11 |
| H27 | 3 | Colonies with different stable ITS2 profiles follow different seasonal symbiont-density trajectories | withdrawn | its2, physiology | Peve, Ptuh | H10 |
| H13 | 4 | A single latent factor spanning all omics layers separates summer from winter samples | not supported | genes, mirna, lncrna, cpg, metabolomics, lipidomics | Apul, Peve, Ptuh | H01, H04 |
| H14 | 4 | Seasonal shifts in storage lipids and central metabolites track host biomass and calcification | inconclusive | lipidomics, metabolomics, physiology | Apul, Peve, Ptuh | |
| H18 | 4 | Gene-body methylation and cis-lncRNA expression explain largely independent parts of within-colony expression change | not supported | cpg, lncrna, genes, annotation | Apul, Peve, Ptuh | H06, H17 |
| H19 | 4 | Colonies with higher methylome turnover have lower host biomass and storage-lipid reserves | not supported | cpg, genes, physiology, lipidomics, metabolomics | Apul, Peve, Ptuh | H04, H14 |
| H22 | 4 | Expression at one timepoint forecasts next-timepoint physiology at held-out sites better than physiology alone | inconclusive | genes, physiology | Apul, Peve, Ptuh | H09 |
Hypothesis status board
Built against MOSAiC commit 86432e3; upstream lock last updated 2026-10-07. Rules for adding a hypothesis are in CLAUDE.md.
Tiers
- Variance structure. Colony vs season vs site. Everything downstream depends on these.
- Regulatory layers. Methylation, miRNA, lncRNA.
- Phenotype and environment. Physiology, symbionts, thermal history, nutrients.
- Integration. Multi-omics factors and energetics.