Richard Feynman in his lectures on physics, said, "How do we know there are atoms? By one of the tricks mentioned earlier: we make the hypothesis that there are atoms, and one after the other the results come out the way we predict, as they ought to if things are made of atoms."It's a genetic fact.
You claim that "common descent is not an assumption. It's a genetic fact." Yet the truth is that the premise was totally accepted as true long before we could access the genome.
So why in order to make it appear as such, do we need to develop computer programs to pull apart the human and chimp genomes at certain places to allow for the bases to look as if they line up leaving apparent differences in sequences contained in one and not the other which are then explained as insertions and deletions?
You can CLAIM a deletion in these intelligently manipulated versions of the actual genomes but to actually demonstrate a deletion you must first show where they once were there and now are not....as for alleged insertions you must show when they once were not and now are, and you cannot, therefore the devised conclusion IS assumption based.
Some actual insertions and deletions do in fact occur but many (not all) are just an illusion created by this intended program.
One researcher (I forget his name at the time but I will look for the study) eliminated the matching "program" (devised by people already convinced) and strung the sequence of bases side by side and when this is done you end up with about a 24% difference in comparative base pairs (that's about 750,000,000 differences). Another taking into account other factors seemingly ignored was suggesting as much as a 70+% amount of differences.
So though in the second example in Barry's article (which had the CERV30 example) we see in the chimp genome a blank space about five letters long (which space is contrived via the program which pulled it apart here to create a match) in reality that space does not exist, it is one continuous unique stream of base pairs, which if undisturbed by those trying to create the Common Ancestor illusion (which may OR may not be true) throws off the order and alleged synchronicity of all that follow...
I am suggesting (and for such reasons as just mentioned) that there may be no deletion here at all (unless you can show something to previously having been there in that genome) and that this (without the false space) is just a normal sequence in their genome which is different in the human genome...
and that this same reasoning should be applied to insertions as well (as many are NOT anything more than normal, ever present, parts of the respective creature's genome). And to show them as actual "INSERTions" one has to show examples of when they were not there previously and now are.
If it is true then this should be no problem. So I am willing to concede I am incorrect (as I have sometimes done even on this forum which I believe Barry cannot do) if you can show me these "deletions" were actually there once, and/or that the "insertions" were previously not.
AND if this discrepancy or alternative yet totally logical reasoning alludes you so much as to fall back on "It must mean there was a Common Ancestor of both creatures" then fine I am willing to concede that point as soon as you produce your example of this so we can compare and see the same criteria met in that creature (not there then there, or once there and then not there)...
Simple right? If a truth, then there should be no problem on your part, so let's SEE? I will await either of you producing this PROOF of your claim.
Similarly, we make the hypothesis of common ancestry, and acknowledge the observed fact that genomes have been subject to insertions and deletions, and hey presto! Virtually all ERVs in the genomes of chimps and humans align. In sequence. They also appear adjacent to the same or similar host genetic material and have the same content. That is sufficient to confirm the hypothesis is correct. Here is "Evolutionary Model" making the same point, and referencing the relevant literature. ERVs
Besides the above, you have a serious problem in explaining how and why these elements could have otherwise come to be where they are. Yes, some components serve useful and sometimes even vital functions. But what's all the rest of it for? And what is so important about its positioning?
And again, I make no apology for repeating the link explaining why everyone except those with a quasi-religious "objections" concludes that ERVs are the inherited remains of endogenized proviruses. You have addressed none of this. Veritas: ERV FAQ: Why do virologists and geneticists think that ERVs come from retroviruses? Isn't that just supposition on their part?
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