I currently have mutation data for a small patient cohort, for a particular gene, in VCF format. My goal is to visualize the frequency or how many times the variant appears in the gene on the genome browser or IGV without the data being so scattered and would much like to create somewhat of a manhattan plot. Any tips on how to do this?
do You have one VCF per sample ?
No, a VCF with multiple samples
You could submit your variants in VCF format to CRAVAT (http://www.cravat.us/ ). It has an interactive variant viewer.
Wow. This tool is amazing. Love it!
Glad that you liked it.