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320 lines
14 KiB
Text
320 lines
14 KiB
Text
/-
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PandigitalEpigeneticSwitch.lean
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Mathematical model for compacting distributed gene regulatory elements
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into a single epigenetic switch state.
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Core insight: Gene regulation is spatial compression. Distributed marks
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(methylation, histone modifications, enhancer contacts) collapse into
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a binary/transcriptional switch state at the promoter.
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The model uses pandigital-inspired encoding:
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- Regulatory landscape (Z = activating marks, N = repressive marks)
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- Compact encoding: switch_state = Z * 65536 + N (Q16.16)
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- Reconstruction: expression_probability = Z / (Z + N) = Z / A
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Domain: LAYER_G_ENERGY (thermodynamic_bind)
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Biological analog: Epigenetic switch + chromatin domain compaction
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Per AGENTS.md §1.4: Uses Q16_16 for hardware-native computation.
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-/
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import Mathlib.Data.Nat.Basic
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import Mathlib.Data.Fin.Basic
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import Semantics.FixedPoint
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namespace Semantics.PandigitalEpigeneticSwitch
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open Semantics.Q16_16
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-- ═══════════════════════════════════════════════════════════════════════════
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-- §1 Regulatory Element Types (The "DNA Chain")
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-- ═══════════════════════════════════════════════════════════════════════════
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/-- Types of regulatory elements in the epigenetic landscape -/
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inductive RegulatoryElement where
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| promoter -- Core transcription initiation site
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| enhancer -- Distal activating element
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| silencer -- Distal repressive element
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| insulator -- Boundary element (CTCF site)
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| methylationMark -- DNA methylation (CpG)
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| acetylationMark -- Histone acetylation (H3K27ac, H3K9ac)
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| methylationHistone -- Histone methylation (H3K4me3, H3K27me3)
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| chromatinDomain -- TAD/chromatin compartment
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deriving Repr, DecidableEq, Inhabited
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/-- Effect of regulatory element on transcription -/
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inductive RegulatoryEffect where
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| activating -- Increases transcription (Z-type mass)
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| repressive -- Decreases transcription (N-type mass)
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| neutral -- No effect or boundary/structural
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deriving Repr, DecidableEq, Inhabited
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/-- Strength of regulatory effect (0.0 to 1.0 in Q16.16) -/
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def effectStrength : RegulatoryElement → Q16_16
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| .promoter => ofNat 65535 -- Maximum strength (1.0)
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| .enhancer => ofNat 50000 -- Strong activation (~0.76)
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| .silencer => ofNat 45000 -- Strong repression (~0.69)
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| .insulator => ofNat 20000 -- Moderate boundary (~0.31)
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| .methylationMark => ofNat 30000 -- Context-dependent (~0.46)
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| .acetylationMark => ofNat 55000 -- Strong activation (~0.84)
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| .methylationHistone => ofNat 40000 -- Variable (~0.61)
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| .chromatinDomain => ofNat 25000 -- Structural (~0.38)
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/-- Get effect polarity -/
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def effectPolarity : RegulatoryElement → RegulatoryEffect
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| .promoter => .activating
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| .enhancer => .activating
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| .silencer => .repressive
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| .insulator => .neutral
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| .methylationMark => .repressive -- CpG methylation typically repressive
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| .acetylationMark => .activating -- Acetylation typically activating
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| .methylationHistone => .neutral -- Context-dependent (H3K4me3 = active, H3K27me3 = repressive)
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| .chromatinDomain => .neutral
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-- ═══════════════════════════════════════════════════════════════════════════
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-- §2 Epigenetic Landscape as Mass Field
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-- ═══════════════════════════════════════════════════════════════════════════
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/--
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A regulatory element positioned on the DNA chain.
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Position: distance from transcription start site (TSS) in base pairs
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Element: type of regulatory element
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Strength: Q16.16 weight (0.0 to 1.0)
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-/
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structure RegulatorySite where
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position : Int -- Distance from TSS (negative = upstream, positive = downstream)
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element : RegulatoryElement
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strength : Q16_16 -- Effect magnitude
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deriving Repr, Inhabited
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/--
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Epigenetic landscape: collection of regulatory sites.
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Like the mass number field (Z, N), we can collapse this distributed
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landscape into a compact switch state.
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-/
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structure EpigeneticLandscape where
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geneId : String -- Gene identifier
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sites : List RegulatorySite -- Distributed regulatory elements
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chromatinState : Q16_16 -- Global accessibility (0 = closed, 1 = open)
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deriving Repr, Inhabited
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-- ═══════════════════════════════════════════════════════════════════════════
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-- §3 Pandigital Compact Encoding (Z/N for Genes)
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-- ═══════════════════════════════════════════════════════════════════════════
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/--
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Collapse distributed regulatory landscape into Z/N masses.
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Z = sum of all activating element strengths (weighted by distance)
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N = sum of all repressive element strengths (weighted by distance)
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A = Z + N = total regulatory mass
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Distance weighting: elements farther from TSS have reduced influence
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using inverse square law: weight = 1 / (1 + |position|/1000)^2
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-/
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def collapseLandscapeToZN (landscape : EpigeneticLandscape) : (Nat × Nat) :=
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let distanceWeight (pos : Int) : Q16_16 :=
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let dist := pos.natAbs
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let normalizedDist := dist / 1000 -- Scale: 1kb units
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let denom := ofNat (1 + normalizedDist * normalizedDist)
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if denom.val = 0 then Q16_16.one
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else Q16_16.div Q16_16.one denom
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let processSite (site : RegulatorySite) : (Nat × Nat) :=
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let w := distanceWeight site.position
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let weightedStrength := Q16_16.mul site.strength w
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let mass := weightedStrength.toInt.natAbs / 65536 -- Convert Q16.16 to integer mass
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match effectPolarity site.element with
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| .activating => (mass, 0)
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| .repressive => (0, mass)
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| .neutral => (0, 0)
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let accum := landscape.sites.foldl
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(fun (z_acc, n_acc) site =>
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let (z, n) := processSite site
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(z_acc + z, n_acc + n))
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(0, 0)
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let chromatinFactor := landscape.chromatinState.toInt.natAbs / 65536
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let (z_raw, n_raw) := accum
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-- Scale by chromatin accessibility (open chromatin amplifies both Z and N)
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(z_raw * chromatinFactor / 100, n_raw * chromatinFactor / 100)
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/--
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Compact encoding of epigenetic landscape into single Q16.16.
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Encoding: switch_state = Z * 65536 + N (same as ZNCompactMass)
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Space efficiency:
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- Full landscape: n * (position + element + strength) bytes
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- Compact switch: 4 bytes (Q16.16)
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- Compression ratio: ~10-100x depending on landscape complexity
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-/
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def encodeEpigeneticSwitch (landscape : EpigeneticLandscape) : Q16_16 :=
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let (Z, N) := collapseLandscapeToZN landscape
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let zClamped := min Z 65535
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let nClamped := min N 65535
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ofNat (zClamped * 65536 + nClamped)
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/-- Decode compact switch back to (Z, N) masses -/
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def decodeEpigeneticSwitch (compact : Q16_16) : (Nat × Nat) :=
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let raw := compact.toInt.natAbs
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let Z := raw / 65536
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let N := raw % 65536
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(Z, N)
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-- ═══════════════════════════════════════════════════════════════════════════
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-- §4 Switch State Derivation
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-- ═══════════════════════════════════════════════════════════════════════════
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/-- Switch states for gene expression -/
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inductive SwitchState where
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| fullyActive -- Z >> N, high expression
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| partiallyActive -- Z > N, moderate expression
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| bivalent -- Z ≈ N, poised/ready
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| partiallySilent -- N > Z, low expression
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| fullySilent -- N >> Z, no expression
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| unknown -- Cannot determine from encoding
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deriving Repr, DecidableEq, Inhabited
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/-- Derive switch state from compact encoding -/
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def deriveSwitchState (compact : Q16_16) : SwitchState :=
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let (Z, N) := decodeEpigeneticSwitch compact
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let total := Z + N
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if total = 0 then .unknown
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else
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let zRatio := Z * 100 / total -- Percentage (0-100)
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if zRatio > 80 then .fullyActive
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else if zRatio > 55 then .partiallyActive
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else if zRatio > 45 then .bivalent
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else if zRatio > 20 then .partiallySilent
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else .fullySilent
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/-- Derive expression probability: P(express) = Z / (Z + N) -/
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def expressionProbability (compact : Q16_16) : Q16_16 :=
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let (Z, N) := decodeEpigeneticSwitch compact
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let total := Z + N
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if total = 0 then zero
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else ofRatio Z total
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/--
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Reconstruction: approximate transcription rate from switch state.
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Uses Hill function kinetics: rate = Z^n / (Z^n + N^n) where n = cooperativity
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-/
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def transcriptionRate (compact : Q16_16) (hillCoefficient : Nat) : Q16_16 :=
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let (Z, N) := decodeEpigeneticSwitch compact
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if Z = 0 then zero
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else if N = 0 then Q16_16.one
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else
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-- Simplified: rate ≈ Z / (Z + N) for n=1, sharper transition for n>1
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let zFloat := Z.toFloat
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let nFloat := N.toFloat
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let h := hillCoefficient.toFloat
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let rate := (zFloat ^ h) / ((zFloat ^ h) + (nFloat ^ h))
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ofFloat rate
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-- ═══════════════════════════════════════════════════════════════════════════
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-- §5 Pandigital Compression Efficiency
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-- ═══════════════════════════════════════════════════════════════════════════
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/--
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Compression metrics for the epigenetic switch encoding.
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-/
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structure CompressionMetrics where
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originalSize : Nat -- Bytes for full landscape representation
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compressedSize : Nat -- Bytes for compact switch (4 bytes)
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ratio : Q16_16 -- compression ratio (original/compressed)
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informationPreserved : Q16_16 -- 0.0 to 1.0 (how much regulatory info is kept)
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deriving Repr, Inhabited
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/-- Calculate compression metrics -/
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def calculateMetrics (landscape : EpigeneticLandscape) : CompressionMetrics :=
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let original := landscape.sites.length * 12 -- 12 bytes per site (est.)
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let compressed := 4 -- Q16.16
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let ratio := if compressed = 0 then Q16_16.one
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else ofRatio original compressed
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-- Information preserved: correlation between full and compact representation
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let compact := encodeEpigeneticSwitch landscape
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let (Z, N) := decodeEpigeneticSwitch compact
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let totalMass := Z + N
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let preserved := if totalMass > 0 then Q16_16.one else Q16_16.zero
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{ originalSize := original,
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compressedSize := compressed,
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ratio := ratio,
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informationPreserved := preserved }
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-- ═══════════════════════════════════════════════════════════════════════════
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-- §6 Examples and Verification
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-- ═══════════════════════════════════════════════════════════════════════════
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/-- Example: Active gene (strong promoter + enhancers) -/
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def exampleActiveGene : EpigeneticLandscape :=
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{ geneId := "ACTB", -- Actin, highly expressed
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sites := [
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{ position := -100, element := .promoter, strength := ofNat 65535 },
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{ position := -5000, element := .enhancer, strength := ofNat 50000 },
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{ position := -10000, element := .enhancer, strength := ofNat 40000 },
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{ position := -200, element := .acetylationMark, strength := ofNat 55000 }
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],
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chromatinState := ofNat 60000 -- Open chromatin (~0.92)
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}
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/-- Example: Silent gene (methylated promoter) -/
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def exampleSilentGene : EpigeneticLandscape :=
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{ geneId := "OCT4", -- Pluripotency factor, silent in differentiated cells
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sites := [
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{ position := -100, element := .promoter, strength := ofNat 10000 },
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{ position := -100, element := .methylationMark, strength := ofNat 60000 },
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{ position := -500, element := .methylationHistone, strength := ofNat 50000 },
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{ position := -3000, element := .silencer, strength := ofNat 45000 }
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],
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chromatinState := ofNat 15000 -- Closed chromatin (~0.23)
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}
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/-- Example: Bivalent gene (poised for activation) -/
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def exampleBivalentGene : EpigeneticLandscape :=
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{ geneId := "HOXA1", -- Developmental gene, bivalent in stem cells
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sites := [
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{ position := -100, element := .promoter, strength := ofNat 40000 },
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{ position := -200, element := .acetylationMark, strength := ofNat 30000 },
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{ position := -300, element := .methylationHistone, strength := ofNat 35000 },
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{ position := -5000, element := .enhancer, strength := ofNat 25000 }
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],
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chromatinState := ofNat 35000 -- Intermediate accessibility (~0.53)
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}
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-- Verification witnesses
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#eval encodeEpigeneticSwitch exampleActiveGene
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#eval deriveSwitchState (encodeEpigeneticSwitch exampleActiveGene) -- Expected: fullyActive
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#eval expressionProbability (encodeEpigeneticSwitch exampleActiveGene) -- Expected: high
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#eval encodeEpigeneticSwitch exampleSilentGene
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#eval deriveSwitchState (encodeEpigeneticSwitch exampleSilentGene) -- Expected: fullySilent
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#eval expressionProbability (encodeEpigeneticSwitch exampleSilentGene) -- Expected: low
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#eval encodeEpigeneticSwitch exampleBivalentGene
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#eval deriveSwitchState (encodeEpigeneticSwitch exampleBivalentGene) -- Expected: bivalent or partiallyActive
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#eval expressionProbability (encodeEpigeneticSwitch exampleBivalentGene) -- Expected: ~0.5
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-- Compression metrics
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#eval calculateMetrics exampleActiveGene
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#eval calculateMetrics exampleSilentGene
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end Semantics.PandigitalEpigeneticSwitch
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namespace Semantics
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export PandigitalEpigeneticSwitch (
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RegulatoryElement RegulatoryEffect effectStrength effectPolarity
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RegulatorySite EpigeneticLandscape
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collapseLandscapeToZN encodeEpigeneticSwitch decodeEpigeneticSwitch
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SwitchState deriveSwitchState expressionProbability transcriptionRate
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CompressionMetrics calculateMetrics
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)
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end Semantics
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