Greetings,
I am writing because I am using multiple SV calling tools to detect both consensus and heterogeneity in structural variants in Mycobacterium tuberculosis. Is there a setting or a flag allowing me to change variant allele frequency, allowing me to detect heterogenous structural variants after mapping the reads to its own consensus de novo assembly?
Greetings, I am writing because I am using multiple SV calling tools to detect both consensus and heterogeneity in structural variants in Mycobacterium tuberculosis. Is there a setting or a flag allowing me to change variant allele frequency, allowing me to detect heterogenous structural variants after mapping the reads to its own consensus de novo assembly?
Thanks, Tristan