Hey guys, I always get confused as to what exactly I have to use when im doing HW.. for example using q vs q^2. Can someone please give me a quick example explaining the differences between p+q and (p+q)^2
Hey guys, I always get confused as to what exactly I have to use when im doing HW.. for example using q vs q^2. Can someone please give me a quick example explaining the differences between p+q and (p+q)^2
Okay first of all q is the allele for recessive gene.
q^2 is the recessive phenotype
p is the allele for the dominant gene
p^2 is the dominant phenotype
So let's say you have an autosomal disease where A represents the dominant allele for hmm normal hemoglobin but a represents the recessive allele for sickle cell anemia....
So a would be = q
aa which would be the sickle cell disease or the percent of people that have the sickle cell disease = q^2
A would be =p
AA would be the phenotype for the individuals that are homozygous dominant for normal and this = p^2
2pq would be the heterozygous guys which would be NORMAL since p is dominant over q and for q that is the recessive allele to exhibit the disease you much be qq / (aa) / q^2 👍
ok so basically if they say.... there is a recessive disease that affects 16/400 people - that would be the q^2 not the q, since its the frequency of the phenotype, right?......
I had the same difficulty. Don't worry if q or p is recessive or dominant that's arbitrary. q is the frequency of the allele and q^2 is the frequency of phenotype or trait, so your right. The way I remember it is just to use probability, if the probability of getting r from a gene pool is 0.2 then getting rr the recessive phenotype should be 0.2*0.2 (or q^2).
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