Hi!
I am a newbi and I am having following problem in biostats.
I have two data sets containing n number of genomic regions.
Set A has 23706 genomic coordinates and Set B has 14557 genomic coordinates. An overlap of this dataset gives 10752 genomic coordinates to be common to both, I want to know what is the statistical significance of this overlap.
I was suggested to apply hypergeometric test in R but unfortunately I am unable format an input for it. Could anyone help me.
Thank you in advance.
I am a newbi and I am having following problem in biostats.
I have two data sets containing n number of genomic regions.
Set A has 23706 genomic coordinates and Set B has 14557 genomic coordinates. An overlap of this dataset gives 10752 genomic coordinates to be common to both, I want to know what is the statistical significance of this overlap.
I was suggested to apply hypergeometric test in R but unfortunately I am unable format an input for it. Could anyone help me.
Thank you in advance.