Looks useful!
http://nar.oxfordjournals.org/content/early/2013/11/24/nar.gkt1188
It look as though the data are now ready for download
http://datasets.pacb.com/2013/Human10x/READS/index.html along with a brief description of the data
http://blog.pacificbiosciences.com/2013/10/data-release-long-read-shotgun.html
http://www.plosgenetics.org/article/info%3Adoi%2F10.1371%2Fjournal.pgen.1003709#pgen-1003709-g006
This paper discusses gene intolerance score — very similar to depletion of common polymorphisms. They don’t analyze non-coding regions — this is using exome data only. Blue for tolerant and red for intolerant (see Figure 1) .
http://news.sciencemag.org/scienceinsider/2013/06/-qa-david-altshuler-on-how-to-sh.html
But how will a little player participate in this? MT @gtyrelle: Q&A: on How to Share Millions of Human Genomes http://bit.ly/19jlKNs
http://www.nature.com/ng/journal/vaop/ncurrent/full/ng.2658.html Uses only CG data for variation, only TFBS data form ENCODE. QT:”the binding sites of several transcription factors show clear evidence of adaptation.”
Hum Genet. 2012 Oct 10.
Ostrer H, Skorecki K.
Departments of Pathology and Genetics, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
http://www.ncbi.nlm.nih.gov/pubmed/23052947
Admixture analysis