Hi,
I am currently working on schizophrenia genomic data from case/control study looking for potential patogenic variations. I used these statistics test to check for significant variations:
Fishers exact test - I have only 95 subjects; from scipy Fst statistics - to check how different case from control groups are; I used it because the study have not CS:CN ratio not equal 1:1, but 2:1; from vcftools Odds ratio - to measure association of variation between CS and CN subjects ; from scipy
I have trouble with interpretation with interpretation of Odds ratio inf values. I mistakenly delete them, but i noticed that I have multiple alternatives only in CS group so the inf value is actually division by zero.
What's the best way to interpret these inf odds ratio values accurately?
I am thinking to only extract the inf Odds ratio values to separete table, and check for significance with the Fisher exact test. But it seems to me too simple.
Thanks you for your answer. But according that links interpretation of inf odds ratio is up to hypothesis of the researcher.So my solution is actually correct. But there is a big question, the data from disease what I am working at is rare. So the ratio CS:CN was probably done to increase strength of study and I should consider even one heterozygot in case group like positive result.