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Hello,
I have tried multiple tools to call structural variants like Manta, Delly etc. They all have a germline or somatic mode.
I couldn't find this information anywhere but anybody know how these structural variant callers determine how a variant is a germline or somatic one ? What are the criteria ?
Thanks for your answers.
do you have paired normal-tumor samples ?
I am working with a non model species and don't have a normal-tumor samples.
But rather 2 haplotypes, and I am expecting one haplotype (let's call it hap B) to have a specifc inversion. Do you think I can "transpose" it like a normal-tumor samples so that would be hap A for normal and hap B for tumor ?