Contact: Lisa Rossi Phone: 412-647-3555 Mobile: 412-916-3315 Fax: 412-624-3184 Tel Alan Aldingerovarian cancer.r for breast cancerAn Australian research team from the Peter MacCallum Cancer Centre, responded to the University of Melbourne and the University of Queensland identified a new risk factor for developing breast cancer. Online online in the journal Cancer Prevention Research.

The research was funded by the United States Department of Defense and National Institutes of Health, the Cancer Council Victoria, the National Health and Medical Research Council of Australia, Susan G. Komen for the Cure and the National Breast Cancer Foundation of Australia.

‘This is very important for understanding the mechanisms of the development of breast cancer as it could drive the development of breast cancer in the same way as a mutation in particular unanswered, in particular what triggers this epimutation and whether women who so risk factor risk factor can reduce their risk by dietary or pharmacological intervention. ‘.

IFATS, the only interdisciplinary fat tissue society to support the development of new technologies derived from and devoted toward adipose tissue.In addition to the purchase contract, announced the Genome Sequencing Center and Rochester of Center participation in Early Access Program for new technological progress for Genome Sequencer FLX System Early access program will be presented Friday, February the advances. Into Genome Biology and Technology Conference into Marco Iceland, Florida.

As part of the on early access program, the Genome Sequencing Center is planning more strains from Caenorhabditis elegans, up a small nematode worm, the previous use as genetic model organisms resequence. – By sequencing different strains of C. Elegans, we will able recognize not only the smaller genetic variation in including single nucleotide polymorphisms, but to identify to larger genome surroundings that can also contribute phenotypes, said Wilson. Having to the longer 400 base Couples reviews read lengths, we can begin to the genomes of with a de novo approach to deleted the need to assemble that sequences of connected to a reference genome which can lead to errors to remap. .