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:
There are three
Explanation:
a large natural or artificial lake used as a source of water supply.
a supply or source of something.
a place where fluid collects, especially in rock strata or in the body.
The answer is pollution, because solar energy is costly, difficult to maintain, and fairly complex.
Answer:
Mitosis is where a solitary cell isolates into two indistinguishable little girl cells (cell division). During mitosis one cell? partitions once to shape two indistinguishable cells. ... If not amended as expected, botches made during mitosis can bring about changes in the DNA? that can conceivably prompt hereditary issues?
Explanation:
