We trace our lineage, biblically speaking, to this essential forebear (Adam and Eve) in that genetically speaking, we are all related. Although scientists have long recognised that, despite physical differences, all human populations are genetically similar, the new work concludes that populations from different parts of the world share even more genetic similarities than previously assumed. (Note the relationship between phenotype and genotype). All humans are 99.9 per cent identical and, of that tiny 0.1 per cent difference, 94 per cent of the variation is among individuals from the same populations and only six per cent between individuals from different populations.
yes that includes the apes who has 99.9999% similar to our DNA's.
as you have clarified before, biblical does that mean let the bible answer it. so does this mean these are all your assumptions and not biblical?
All creation shares the same universal truth. Which is seen in the process of TT (transcription and translation) of genes. The processesing of RNA to DNA (and the reverse transcriptase abilities) and the transcription into proteins (mature RNA).
Humans are similar in that we all, as a species share 23 pairs of chromsomes; and when it goes through the meiotic/mitotic duplicaiton, becomes 46 pairs of sister chromatids. And then in the meiotic processes, becomes and observes the haploidy (the splitting of diploids to haploids). Thus preparing the species to undergo gametogenesis.
Humans are different from other primates in that we have 23 pairs of chromsomes. Other primates such as chimps, gorillas, orangutans have 24. Thereby implicating a complete difference if genetic variance and thus inable to proliferate. All primates have similar numbers of chromosomes.
(By you saying that chimps have 99.99% of human DNA is in err; rather what scientists and geneticists are saying is that chimps have the same replicative processes as other eukaryotes (humans, being the apex of organogenesis, shares in this due to the eukaryotic universalism of eukaryotic species). It is the same as how humans, apes, and flies share similar homeobox; meaning the universality of the Trinucleotidic base pairs. Leading to the fact that all creation shares similarity in trinucleotidic repeats; and deviation of those repeats leads to mutative manifestations. (frame shift, or deleterious repeats).
Humans, in pathological conditions may have a lacking of one chromosome or deletion of one; particularly in cases of Trisomy 21 (Down Syndrome), which manifests clinically into cardiac deficits, mental retaradation, as well as phenotypic deviation from norm; seen in the presence of simean crease, as well as increased evidence of epicanthal eye folds and susceptibility to develop leukemias and immunological sequelae.
Linkback: https://tubagbohol.mikeligalig.com/index.php?topic=11214.msg337088#msg337088
