It's painfully technical...
OK, well stop if it hurts too much, we wouldn't want you to injure yourself...
...it's basically allowing us to model off pre-existing designs that are proven to function which scientists are currently using as the foundation to build nanomachines that can exclusively attach to cancer cells to inject medicine or to further drill into the cancer cell's membrane to kill it.
My understanding is that rather build nanomachines from scratch, they're using modified bacterial mechanisms such as
CRISPR Cas9, but I'd be interested to see a link or reference to what you describe.
...You can continue to watch the video provided in the OP as your reference and introduction on what modern biologists are discovering inside a cell. He starts describing these design patterns at 43:30 minutes into the video. Let me know if this is like velcro in your honest opinion.
OK, I watched that part of the video - and I can see you just used Meyers' misleading description of design patterns verbatim. Dixon's discovery of the complexity of generic code transcription is nothing new, and a major factor in its efficiency and 'elegance' is that it doesn't really function like computer code (whatever Bill Gates may have said) but more like an industrial demand economy...
I asked you what particular design patterns we could use because, to my knowledge (I've used design patterns in software development for 20+ years), we already have our own implementations of automated error correction (as I said, not in itself a design pattern), hierarchical filing, and nested coding, that are well suited to our computer architectures and resources.
As for overlapping reading frames, overlapping code sequences were experimented with at the dawn of computer programming, but are pretty much unmaintainable. Self-modifying code is still used in special circumstances, so it's possible some overlapping code is in use, but without the storage restrictions of early computing systems, there's generally no good reason to use it. As it happens, overlapping reading frames are expected to have evolved in the genome because of the way transcription (assembly of mRNA) control differs from translation (protein assembly) control - see
Start & Stop Codons for an overview.
As I explained previously, Velcro is the commonest biomimetic in everyday use, and hook & loop is a design pattern, so it has 'being a design pattern' in common with other design patterns. You suggested that we could make biomimetic use of the genomic design patterns, but you haven't yet given an example - I'm sceptical because of the major differences between genome processing and computer processing architectures, but I'm interested to hear your suggestions.
... It's that inference to the best explanation which is that the creation of new information is habitually associated with conscious activity.
If you're suggesting that a claim of 'habitual association' somehow makes a testable hypothesis, you'll have to explain how you reach that conclusion. But in any case, new information is only associated with consciousness by people who don't understand information.
Information is inherent in the arrangement of matter - if the arrangement changes, the information changes; if the arrangement is new the information is new; new information is produced continually in nature. This is why it's so fundamentally related to entropy. If you were instead referring to Dembsky's hokey 'Complex Specified Information', that too has been shown to be produced by natural processes, so consciousness is not a requirement.
The main point here is the origin can be accounted for on these issues of phenotypic complexities and anatomical novelties that cannot be explained by the evolutionary processes I touched upon in post #30. These problems were outlined by prominent evolutionary thinkers such as Professor Gerd Muller at the Royal Society of London, and he made a list of the explanatory deficits of modern synthesis. (modern synthesis is another name for neo-Darwinism.) And almost all of which had to do with the lack of creative power surrounding the famed natural selection and random mutation mechanism.
You didn't supply any references, so I don't know what specific problems were raised, but if you're referring to Shapiro's work, he's arguing that known processes (e.g. epigenetics, genome doubling & restructuring, symbiogenesis, HGT, inter-specific hybridization) play a larger role in cellular evolution than the neo-Darwinian synthesis suggests. His views are more extreme and so more controversial than most, but it's clear these processes have some influence, it's a matter of establishing the degree; it's early days. But the underlying principle of evolution by natural selection still applies.
TBH I find these statements unwarranted as it is based on conjecture and a misrepresentation of the arguments. I also can't help but see a bit of double standard being placed upon the same method of reasoning used by Charles Darwin himself. You are welcome to go point by point using neo-Darwinism as a comparison, but you may surprise yourself on realising that the scientific method debunks neo-Darwinism.
Expressing dissatisfaction is not an argument. You're quite welcome to show your own abductive analysis, or counter mine. If you think I'm misrepresenting the argument, by all means show how I'm doing so.
Junk DNA
When the genome was decoded back in 2000 it was discovered that only 2% of the genome coded for proteins and the other 98% was dismissed as junk.
Citation? You do realise that the term 'junk DNA' was coined in the 1960's, and formalized in 1972 ?
But when the results of over 1,600 experiments by 450 scientists from 32 different institutions discovered that the 98% that people thought were junk, wasn't junk at all, but absolutely essential for the maintenance of life. The opinion pieces you provided seem to suggest that prominent scientific journals "misrepresented the position of junk DNA" which I find no evidence of, rather a display of a shifting of the goal posts - yet for whatever reason, the goals here are not in favour toward neo-Darwinian ideas.
Perhaps I didn't explain clearly enough. ENCODE study identified that much 'junk DNA' is transcribed and translated; but the products are not
biologically functional, i.e. it produces harmless junk. They say their concern was to identify products that might affect medical treatments, e.g. drug interactions.
'Junk DNA' is not 'absolutely essential for the maintenance of life' - experiments have shown that
at least 3% can be deleted with no noticeable effects. Some parts of it are known to have undergone exaptation to acquire biological functionality, but deleterious mutations set a limit for the number of functional loci in non-conserved areas.
Some non-coding junk DNA, the
'satellite DNA', does appear to have a structural role in packaging chromosomes in the nucleus, which explains why it is more highly conserved than the rest.