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.
The correct option is this: A STUDY BY DR BIRDIE SHOWED THAT THE NUMBER OF SONGBIRDS IN HER YARD INCREASED DUE TO A MODIFIED FOOD SOURCE.
A scientific claim refers to a claim that is made by a scientist due to the result that he or she obtained in the research that are conducted. In the excerpt given above, it can be seen that Dr Birdie experience influx of songbirds to her yard as a result of the dried apple and the raising that she added to the birds' food.
