First open the folder with the hg19 datasets by clicking on the blue
triangle next to the folder name (red arrow pointing up). In this
library there are currently two sets of full-coverage SNPs from
healthy individuals. One has 24 public genomes from a variety of
sources, populations, and sequencing technologies. The other is a
group of 69 from Complete Genomics (blue arrow). In most cases you
will want to use both of these for filtering; however since our
example input dataset is based on one of the CG genomes, we'll skip
that set here. To import datasets into your history, check the ones
you want (red arrow) and then click the Go button (green arrow).
![[screen shot]](snpLibraryWithArrows.png)