Answer:
C. This is an example of VNTRs.
Explanation:
VNTRs are Variable Number Tandem Repeats. These are short sequences of DNA repeated in tandem (that is, the sequences are repeated one next to the other) a certain number of times. Unrelated individuals have a different number of repetitions for a certain region of the DNA, therefore the total length of the fragment is variable among individuals, depending on how many times the short sequence is repeated.
The compound eyes of insects <span>detect color and form images. The correct option among all the options that are given in the question is the first option or option "A". The other options are close but they are incorrect. I hope that this is the answer that has actually come to your help.</span>
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.
