I have RNASEQ data from from cells that have underwent a knockout treatment using CRISPR-CAS9. I've aligned the data using RUM and did differential expression analysis. Now I want to look at off-target mutations caused by CRISPR and if they can account for the difference in gene expression. How would I go about doing this?
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For calling variants, try: http://gatkforums.broadinstitute.org/wdl/discussion/3892/the-gatk-best-practices-for-variant-calling-on-rnaseq-in-full-detail
Then your typical eQTL analysis...?
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