Hi,
We're working on benchmarking LongGF on simulated long read data generated using badread. There are a minority of fusions which appear to not get detected where the fusion partners originate on opposite strands of DNA. The mutation in these cases I guess would be fusion with an inverted sequence, can you LongGF correctly call these kinds of compound mutations?
Hi,
We're working on benchmarking LongGF on simulated long read data generated using badread. There are a minority of fusions which appear to not get detected where the fusion partners originate on opposite strands of DNA. The mutation in these cases I guess would be fusion with an inverted sequence, can you LongGF correctly call these kinds of compound mutations?