The selection is NOT random, as has been explained to you. But, as usual, in one ear, out the other.
what selection has to do with that? im talking about the author choice.
Almost certainly not true. Thatās a excuse, nothing more. Anyway, their analysis focused on sequenced full genomes, which are biased in favor of smaller genomes.
Lungfish have not experienced a recent whole genome duplication but do have lots of active transposable elements. In any case, their haploid genome size is still much larger than ours. See the following paper for details:
The Lungfish Transcriptome: A Glimpse into Molecular Evolution Events at the Transition from Water to Land
lets say that it is true. how it make any difference? remember that their study is about correlation between amount of junk and complexity. the result should represent a pattern no matter what the size of the genome is. if a genome is larger than other genome we should also find a larger part that is junk, even if both genomes are small.
No, that isnāt what their study is about. The correlation is a no-brainer. Their supposed point is a correlation between amount of junk and organismal complexity. And thatās biased by their sample. Humans happen to be among the larger sequenced genomes, just because of the sampling.
how? if i take a bunch of small genomes and i check the proportion of junk and complexity. say that i find out that we see a good correlation between the junk and complexity (number of cell types). isnt it a good estimation?
So am I. The authors chose a minute and non-representative sample of genomes to compare. That makes their data useless.
Only if you assume the correlation exists. You cannot demonstrate the correlation by choosing a non-representative sample.
This is basic, high school level stuff.
we dont need to assume anything. if we take say 100 (small) genomes and we find a correlation between amount of junk and complexity- we then have a good estimation in general.
Of course, we still call it non-coding.
So now that youāve been straightened out on that false equivocation, itās time to decide if your misrepresentation is willful or not.
i think its because of my english.
Not if the reason you only have small genomes to work with also reduces the likelihood that your sample will include organisms with lots of junk in their genomes.
Organisms with small genomes are more likely to have had their genomes sequenced.
Organisms with lots of junk in their genomes are more likely to have large genomes than those without lots of junk.
Can you figure the rest out for yourself?
That doesnāt seem to impede your ability to understand the creationist crap you keep touting.
Iām skeptical, since you edited your response from:
āisnt the term ājunk DNAā was refer to non coding DNA in the first place?ā
to:
āof course that if we find a non coding region that do something we cant call it ājunkā anymore.ā
The answer to the question you deleted is no.
So, do you now understand that the descriptions ānoncodingā and ājunkā do not mean, and never have meant, the same thing?
And that equivocating them is a standard IDcreationist deceptive trope?
The human genome is on the high end of sequenced genome sizes, but itās not at all on the high end of all genome sizes. Thereās your bias right there. Fugu was chosen for sequencing precisely because it has a small genome. Ditto for Arabidopsis, and so on. Thus the bias.
Rule #1 of statistical analysis is that your sample must be representative over the population being studied. If it is not, then you cannot draw any conclusions about the underrepresented portions of the population under study.
You seem not to have had any awareness of this fundamental rule of statistical analysis. Now that you have been made aware of it, do you see why the unrepresentative sample does not permit Sanford to draw a conclusion over the entire biological domain?
I know where Iām placing my betā¦
Neither, I think, The authors do mention that they only looked at a few species when they were considering cell type numbers. That may not have been very clear. As others have pointed out, they looked at a sampling, but it isnāt really proper to consider their sampling to be either random or representative of all species. It is difficult to tell just why the authors chose those species that are in the paper.
The source is pretty resourceful. As I said, this paper is tucked away in an obscure place.
It appears that they chose species with published genomes. There may have been further selection, but thatās the bias I noticed.