Hello,

I'm a medicine student and i'm investigating the effects of a single nucleotide polymorphism on the expression of a phenotype (cuantitative).

I have already performed an ANOVA test to see if there where any significant differences between the groups WT/WT, WT/VT and VT/VT. Out of nearly 200 genes I found 3 genes with statistical significance.

I would continue to perform tests on these genes in order to find out more about the relationship between these genes and the phenotype.

What do you think should be the next step in order to find the impact of having 0, 1 or 2 copies of the allele VT on the phenotype?

What test would you perform and with which data would you present the discoveries to a scientific journal?

Thank you very much in advance.

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