Good day,
I have 2 lists of genes
- Gene list A consists of ~500 differentially expressed genes (DEGs) from a microarray analysis
- Gene list B is a list of 200 susceptibility genes drawn from various GWAS
I have performed pathway over-representation analysis (ORA) on each list using innateDB and found that there were ~150 and ~115 over-represented pathways involving genes from gene list A and B respectively. Now I wish to compare the 2 lists of over-represented pathways for possible overlap.
Using Venny, I have found that ~50 of them overlap but I understand that I also need to perform a statistical test to ensure that this overlap is not just due to chance. However, I am unsure of what statistical test I should perform and how I can go about doing so.
As part of the analysis of these gene lists, I have previously done a hypergeometric distribution test to check for overlap between the genes themselves, but I do not know if this same test can be applied to pathways and if so how should I go about doing it (i.e. I am unsure of how to define the parameters of the hypergeometric distribution test in this situation). I have also read some studies that use Fisher's method to combine the p-values and was wondering if this is the method I should be using.
Unfortunately I have no experience with R. Regardless, thank you for all your help!
Tl;dr: I have overlapped 2 pathway lists and found that they overlap but do not know what statistical test should be used to give evidence that these results are not due to chance.
Edit: I have also read this thread which relates to my question which states that it a suitable test may be a Fisher's F test. However, I don't understand the procedure I need to follow to get my desired p-value.
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weeweedelivery123 •
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Look at this. It computes a hypergeometric distribution (and you don't need to use R). I think you will need the total number of pathways tested from innatedb.
Hello, thanks for your reply!
Just to clarify, I have previously used this test to obtain the p-value for the overlap between the genes themselves in this way:
However only 75% - i.e. 150 of these GWAS genes - are represented on the platform and the overlap of genelist A and B is 15 genes, so my hypergeometric distribution test should be looking for:
The probability of getting 15 or more white balls in a sample of size 150 from an urn with 500 white balls and 16500 black balls, assuming H0. Therefore, I used R with an input: 1-phyper(14, 500, 16500, 150) -- I got this formulae via another forum post
However at this moment in time I am actually more interested in at a test for testing the p-vale for overlapping pathways identified via pathway ORA. I was wondering if you were suggesting that the same test could be applied to pathways in the sense that:
Since I have identified that there are 50 overlapping pathways, my test would be finding the probability of getting 50 or more 'white balls'' in a sample of size 115 from an urn with 150 white balls and (x-150) black balls, assuming H0?
Would the hypergeometric distribution test be valid/the best test in this situation?
EDIT: Rethinking this problem, would a Fisher's exact test work? I assume the 2x2 table would be:
where
x= total number of pathways possible in the innatedb databaseYes, a Fisher's exact test would give you an exact p-value based on your contingency table. There is no difference between your first problem (overlap of input list of genes and genes of a particular pathway) and second problem (overlap of GWAS and DEG pathways).
Using chi-squared test or hypergeometric test is appropriate too but the input table to the software you are using might be different.
Yes, I was actually referring to using the same test (hypergeometric) for pathways as well.
No, I would say a Fisher's test is not applicable to your data. I seriously doubt you can create a contingency table like the one you have shown. Technically it should be (but not possible with your data):
You cannot have one group as column & the other as row (like you have shown).
@weeweedelivery123 have you figure out this problem? I have such problem.
I saw mehran.karimzade has confirmed your answer, but komal.rathi has not confirmed.
I appreciate if you reply.