NGMLR is a long-read mapper designed to align PacBio or Oxford Nanopore (standard and ultra-long) to a reference genome with a focus on reads that span structural variations
Planning on trying NGM-LR to identify structural variations by read mapping PacBio reads to a reference genome, is it advisable to error correct PacBio reads before alignment or is just better to feed the raw data and let NGM-LR do its work? Could not see any info about this in the docs nor posters.
Planning on trying NGM-LR to identify structural variations by read mapping PacBio reads to a reference genome, is it advisable to error correct PacBio reads before alignment or is just better to feed the raw data and let NGM-LR do its work? Could not see any info about this in the docs nor posters.
Thanks, Pedro