Hello All,
I have a genotyping data from Human Omni 1 Quad v1.0 DNA Bead Chip with Demographic Particulars of Cases and Controls. Since i am very new to GWAS , it would be really helpful if you please let me know the ways for Conducting a full GWAS analysis of the raw data, for arriving at SNPs with different p-value (<0.005, < 0.001) data sets, how to have an Association analysis of imputed data and also have a pathway analysis from the SNP data to chart disease relevance.
It would be really helpful if you guys please let me know the pipeline for it and related tools for this analysis !
Thanks a lot for you help !
These two are very good papers for starters to understand statistics and its use in GWAS QC. Thanks a lot for this suggestion. It was very useful.
Thanks a lot for your help, Its really useful.. I have a doubt, Is it possible for arriving pathway-based analysis, report from the derived SNPs?
See edited answer. Please avoid asking extra questions in comments.