Hello,
I sequenced some strains of Ensifer medicae and have mapped them to the reference WSM419 using bwa. Afterwhich I sorted, reordered, etc. using picard. What I want to find out is where along the reference my reads mapped to, as I want to compare and visualize the location and percent of reads mapped between strains (Some strains mapped 85%, some 25%, I want to visualize this if possible).
While IGV is useful, I ideally want to be able to visualize whole chromosomes and plot each strain's coverage around it in circularized plots.
Thanks.