Signature of backward replication slippage at the copy number variation junction.
J Hum Genet. 2014 Mar 20. [Epub ahead of print]
Ohye T, et al.

The authors used chromsomal microarrays to analyze the del(2)(q13q14.2) chromosomal junction site observed in a woman with a recurrent pregnancy loss. They were able to demarcate a 2.8 megabase deletion that does not appear in the database of human genomic variations.

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Researchers describe a way to share data while keeping it secure, Agence France Presse reports.

In Science this week: genetic mutations typically associated with esophageal cancer are common in older, healthy individuals, and more.

India's Council of Scientific and Industrial Research has a new director-general, according to ScienceInsider.

A new study links more than a hundred genes to autism spectrum disorder, Discover's D-brief blog reports.

Oct
25
Sponsored by
Roche

This webinar will detail a comprehensive strategy that a lab has put in place to evaluate  NGS oncology assays for genomic tumor profiling of plasma and tissue samples.