Question

In terms of genome location, what does sequencing accomplish?

a. Locates duplicate regions and genetic loci mutations within a chromosome structure.
b. Locates genome features such as gene inheritance patterns and variants.
c. Locate the position of heritable traits within the context of a chromosomal genetic map.
d. Locate the position of gene (i.e. trait-associated) sequences within the context of a genome

Answer 1

d. Locate the position of gene (i.e. trait-associated) sequences within the context of a genome.

Step-by-step explanation:

d. Locate the position of gene (i.e. trait-associated) sequences within the context of a genome.

Sequencing is a technique used to determine the complete DNA sequence of an organism's genome. By sequencing the genome, we can identify the position of gene sequences that are associated with specific traits, such as diseases or inherited characteristics. This information can help us understand the genetic basis of these traits and potentially develop new treatments or interventions.

While sequencing can also identify duplicate regions and genetic mutations within a chromosome structure, and can help locate genome features such as inheritance patterns and variants, its primary focus is on identifying the specific location of gene sequences within the context of a genome.