Answer:
all of the above
Explanation:
When the human genome was sequenced, one of the first information generated was related to the structure of the genetic material. For example, it has been found that there are long repeated sequences in different parts of the DNA or regulatory parts of its functioning in other parts of the genetic material itself.
When determining the order of nucleotides of a living being and comparing it with others of the same species, we find some regions that accumulate more differences than others, that is, are more diverse than others. Very similar sequences, that is, conserved in all living beings of the same species, can determine essential characteristics of these organisms. These essential characteristics can be very important for many different sectors and improve the lives of humanity in unimaginable ways.
The discoveries made through the complete sequencing of a genome can cause immense improvements in the fields of medicine, agriculture, biofuels and many other fields.
It means that two chromosomes
have the same genes, or variations fo the
same genes at the same loci on the chromosomes. Variation
of the same gene is what makes up
alleles. Homologous chromosomes
are similar in size and structure. In
diploid organisms, each chromosome in the pair is derived from each parent.
The answer is c because you just replace variables of x,y x(-2)+ y(3)
