CNV and network analysis references, human diseases

PubMed ID: 24244640;
CNVannotator: a comprehensive annotation server for copy number variation in the human genome.

PMID:22729399 for PPI;
Proteome-wide prediction of protein-protein interactions from high-throughput data.

PMID:24067414 for gene network,
Gaussian graphical model for identifying significantly responsive regulatory networks from time course high-throughput data.

PMID:22360268 for network-based disease analysis; and
Network-based analysis of complex diseases.

PMID:14735121 for network biology
Network biology: understanding the cell's functional organization.

20150718:
http://www.nature.com/nature/journal/v464/n7289/abs/nature08979.html
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

http://www.nature.com/nature/journal/v464/n7289/abs/nature08516.html
Origins and functional impact of copy number variation in the human genome