The answer is it provides us with vitamins. Hope this helps.
Answer:
SNPs have shown that only 0.1 % of DNA sequences are different in the human genome between different individuals, thereby all the inherited phenotypic variation observed in our species is associated with only 0.1 % of differences at the genome level
Explanation:
Haplotypes are block-like sequences of DNA that are inherited together due to low recombination rates. Moreover, single-nucleotide polymorphism (SNP) mapping is a very useful methodology used to map the site of SNP mutations (i.e., SNP variants). In this regard, it has been observed that there are approximately 10 million common SNPs in the human genome. These SNPs contribute to the wide range of phenotypic variation observed in human populations for different traits (e.g., eye color, hair, weight, height, etc). Moreover, researchers have determined that SNPs can be clustered into haplotypes, thereby haplotypes can be accurately sampled by as few as approx. 300,000 selected SNPs, which are sufficient to represent all of the genetic variation across different human genomes.
Answer:
the answer would be the 3rd answer
Explanation:
a half life is the time it takes for half of a radioactive substance to decay
I hope this helps :)
The condition called dysuria is characterized by painful or difficult urination, it can be due to pathologic or benign causes.
Answer:
(A) speciation.
Explanation:
Shrinking of water bodies and development of deserts since the Pleistocene ice age produced new vacant niches that could be inhabited by organisms such as fishes. Production of new isolated streams, ponds, and springs allowed the fishes to occupy these new water bodies. Accumulation of genetic variations to become adapted to their new habitat resulted in the evolution of several new species of fishes with many different genetic traits. This represents speciation due to geographical isolation.
