Entering edit mode
5.1 years ago
printingdots
•
0
I am new to this area and I went through some tutorials and software on how to simulate and format my own TWAS data. However, I noticed that most software do not produce the N column in the output. I understand how we are getting CHR, BP, SNPs, allele columns and Z/p-score statistics. Please can someone explain how we get different values of N for different SNPs?
Edit: I should mention that I'm trying to generate TWAS based on .bim/.fam/.bed files
What do you mean by N ?
Number of samples of each SNP
Are you talking about Transcriptome Wide Association Studies ? What softwares are you talking about ? No. of samples for each SNP ? Or the sample size required to perform TWAS ?
Resolved. It was number of samples for TWAS.