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:
You told us the answer to your own question
Explanation:
You put answer :B
Double layered nuclear, the outer nuclear membrane is continuous with the membrane of the rough endoplasmic reticulum (ER), it also continues with the inner nuclear membranes since the two layers are fused together at a numerous tiny holes called nuclear pores that perforate the nuclear enevelope
No because if you take that out , it acts like a skeleton so if you take that out, it will spill it contents out and won't really do any thing
Answer:
i dont know sorry,........