A growing number of cytogeneticists are joining a new entity called the Cytogenomics Array Group to share data related to abnormal microarray findings.

CAGdb, the group's database of copy number variants, is the main interface for members who have been enticed to join CAG by the resource's "user-friendly and intuitive interface, search functionality, data output, and community," according to Hutton Kearney, director of the cytogenetics laboratory at the Fullerton Genetics Center at Mission Health in Asheville, NC.

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In PNAS this week: rare variants linked to bleeding disorder, comparison of whole-exome and whole-genome sequencing, and more.

George Church tells The Sunday Times that his group has inserted some woolly mammoth genes into elephant cells.

A Scientific Reports editor resigns over a new policy at the journal allowing researchers to pay to fast track the peer review of their manuscripts, and poll.

The National Cancer Institute's Harold Varmus discusses the state of cancer research with the New York Times.