Hello,
I wanted to inspect the (non-N) regions that were added in, in GRCh38/hg38 that were not there in GRCh37/hg19. Is there a hg38 bed file with those "new" regions somewhere or is there an easy way to get that without lifting over again?
Thanks for your help!
See these posts:
A: How to determine reference genome that was used for alignment given BAM with obs
A: Convert BED(UCSC) to VCF