Chromosomes

They are a helix, made of a 2D color matching process, driven by spacial charge attraction.

They get bundled as chromosome, with a middle tie of yet another sequence.  The center tie partitions one DNA sequence into a short and long pair. Two sets of these is called a haploid, I think.

  Humans are the second diploid, we have 23 of them.

A Bayesian model. These have to sit in a mostly closed surface, we have to fill in all the layers of the salad bowl.  This should also fit the standard algebraic model notation, it has operations, binary, and rules of combinations over finite sets.

Really, this is an orbital problem also, in fact this whole thing is driven by charge distribution.  Spin exclusion still applies, the smallest of the Markov triples doesn't roll over.   There should be primitive orbits when the chromosome sequence is packed.  Some shapes must be replicated internal, it is still modulo some rational fraction. Alternatively, it must have kinetic energy and be rolling about symmetries.

We can do quick back of the envelope, that surface will not be known better than 1/20, or 2%, it doesn't have more precision.  Compare this to Planks in flat earth, thisd is a relatively very very slow system, but otherwise obeys 3D physics.

The basic correction is on of the sugar phosphates. They come in two colors, really as they are pairs, but via some homomorphic morphing we can make this a tree color with the centroid becoming a color. The docs only describe one form of the structure during meiosis, or mitosis.  But the salad bowl makes more sense, the three types forming a layering about the closed exterior surface of a salad bowl.

I looked up the 23 Markov number, about 15000.  23 would be the number of layers.    That seems in the range that the docs are reporting.

So it is the basic game, minimize the error every six three color selections exchanges, per surface layer. 23 layers fills the salad bowl.  That would be the model of a call nucleus. When an external force, say a layer of lipids? reshaped the salad bowl, it will disconnect ow color pairs from the third. This is equivalent to having colors that are not relative prime, to pairs attempt to rotate out of charge imbalance and collide with another pair in opposite rotation.

These sequences in the salad bowl represent the slope, kinetic energy in the ratio of the rate of emission. That slop still must be as irrational as possible and we are still balancing three binomials.

Light, in this system is still two steps.  But they are slow steps compared to the speed of our flat earth biochemical tools. That is the secret behind micro biology of DNA. Our tools have circular accuracy much better than DNA hyperbolic accuracy. I think something out side the sphere pulls out on one side and in on the other, the effect to concentrate the chromosomes on a source, unfold them. Hold them in that surface position, Markov 24,  and feed them peptides which will make the subsequent 23 Markov shells inside,  once again. Presto, you have a duplication.  When that nucleus is in balloon mode, there must be a mRNA process inside digesting peptides and making the matching Markov set.

This is a topology thing. Having it down to a Lie Algebra speeds up the development of covid solutions. For example, a lie algebra can find optimum paths from one peptide to one protein position.  That path goes straight to the cultures.

If you think about taking two steps across the Markov surface, you notice that is very slow looking to humans an N grows. That is the essence of jumping up the Markov triad. That is the  correction imbalance taking a symmetric kinetikc path.  That path seems an extra dimension until the error imbalance returns to normal. It jump up and down one Markov 3-tuple node, but appears momentarily more accurate as a 4 tuple, is my speculation.. This would be a dimensional jump, jumping from atoms to sugar phosphate sequences. To the next observe up, it is a clear distinction in flat earth, an order of magnitude slower.