Hi everyone.
I aim to identify translocations with ultra-low pass whole genome sequencing (~0,5X).
Im testing DELLY against some public data and DELLY didnt find the same translocations mentioned on papers (wich mention default parameters).
Is there any special data tratment dus to its low coverage?
I'm could see split reads on IGV proving the translocation EWSR1-FLI, but DELLY didn't call it.
How to proceed?
Thanks in advance
My pipleine: FASTQ >Quality check > BWA-MEM (-M paramenter) > DELLY (default)
All of it was done on Galaxy.