A discussion for how the program should handle more complex structural variants. That is, how can one estimate the genomic region to where the reads supporting a variant are aligned in a bam file.
Hi @adrosenbaum , I think we should look at the breakpoints for the structural variations and depending on the type and size we can decide how big the regions to collect should be.
A discussion for how the program should handle more complex structural variants. That is, how can one estimate the genomic region to where the reads supporting a variant are aligned in a bam file.