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.
Artificial Selection or “ Selective Breeding”. aka the process by which humans use animal breeding and plant breeding to selectively
The number of chromosomes will be haploid as opposed to diploid so you will end up with 5 chromosomes
I think it's <span>a=F/m ; F=m/a=1200 kg x 3.0 m/s^2 = 3600 N</span>
The correct answer is this one: "C) Nnew = Nold + 2." A student is studying a process in which a diploid cell becomes haploid. The CORRECT mathematical model for the process if Nnew is the number of chromosomes in the haploid cell and Nold is the number of chromosomes in the diploid cell is this: <span>new = Nold + 2
</span>
Here are the choices.
<span>A)
Nnew = 2·Nold
B)
Nnew =
Nold
2
C)
Nnew = Nold + 2
D)
Nnew = Nold × 2</span>
