00:29:27	XinmingTu:	If we use other technology such as ATAC-seq, will that be different? ( I assume it’s technology dependent, there will be some off-sets if use different technologies)
01:03:59	GGlusman:	I wonder how much of the pattern is 'explained' by %GC
01:10:34	dh:	Is the Hilbert/Peano curve better for visualization than a 2D model gotten from Hi-C?
01:10:52	GGlusman:	@dh indeed!
01:11:41	dh:	let's say a UMAP gotten from Hi-C data, to be concrete.
01:12:05	dh:	Yes
01:12:55	GGlusman:	I thought in a different direction - start from the linear chromosomes, and 'fold them' to maximize Hi-C inter/intra chrom connections
01:13:23	dh:	what  GG said...
01:14:06	dh:	There are hybrid approaches.  E.g. use HiC to generate a rough map, then Hilbertify it.
01:18:31	GGlusman:	love this stuff!