TCGS-SEQUENTIONBiological Proof Protocol: Synchronous Parallel Emergence Testing Using <em>Drosophila</em> and Microbial Data A Comprehensive Falsification Framework with Executable Public-Data Pipelines
Discuss this preprint
Start a discussion What are Sciety discussions?Listed in
This article is not in any list yet, why not save it to one of your lists.Abstract
The TCGS-SEQUENTION framework proposes that observable evolutionary dynamics constitute projections from a higher-dimensional counterspace structure, implying that certain heritable traits may exhibit synchronized emergence across physically disconnected populations beyond what contact mediated mechanisms can explain. This paper presents a comprehensive, falsifiable protocol to test the Sequention hypothesis using existing public genomic data from D. melanogaster and fast-evolving microbial systems, providing a definitive empirical test that yields either support or falsification. We operationalize Synchronous Parallel Emergence (SPE) as the central testable prediction: multiple isolated populations exhibiting coordinated change-points in trait-linked markers within a predefined temporal window, after controlling for migration, shared environmental forcing, and all standard evolutionary mechanisms including soft sweeps, polygenic redundancy, and cytoplasmic hitchhiking. The protocol employs a three-gate falsification structure: (G1) significant synchrony beyond null expectation, (G2) exclusion of directed influence pathways, and (G3) common-cause exclusion with chart invariance. The protocol is executable immediately using the Drosophila Genetic Reference Panel (DGRP), Drosophila Genome Nexus (DGN), Evolve-and-Resequence (E&R) time series, and long-term bacterial evolution datasets. This paper provides a decisive, no-waiting proof attempt: either SPE persists after stringent controls (supporting Sequention), or it dissolves (falsifying the universality claim for these systems). Explicit decision rules, confound matrices, and implementation checklists are provided for independent replication.