You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
Thanks for using cuteSV. You can call SVs on each sample, and then use tools like truvari or surviour to select the SVs that are only included in the tumor sample.
Hi,
Thanks for developing this awesome tool.
I'd like to call somatic structural variants (SVs) using paired tumor and normal samples. However, cuteSV can only process one sample at a time.
I am unsure about the next steps after obtaining the tumor.vcf and normal.vcf files.
Best wishes.
The text was updated successfully, but these errors were encountered: