Entering edit mode
12.1 years ago
C Shao
▴
140
I found many structure variations in the genome sequencing data by breakdancer. Now I am trying to evaluate them visually.
However, the breakdancer seems not to provide information on which pair of reads support the translocation, or other SV. For the information provided by IGV, they are many reads on the interested region.
How do you check the SV in IGV or other genome browser?
Thanks.
duplicate of best genome browser to look at structural variation calls