Sequencing

NEWS For more information: Cathy Yarbrough press@ashg.org 858-243-1814 Embargo: 10:30 a.m. PT, Thursday, Nov. 8, 2012 Research findings confirming that de novo mutations represent a major cause of previously unexplained intellectual disability were presented today (Nov. 8) at the American Society of Human Genetics 2012 meeting in San Francisco. Josep de Ligt, M.Sc., bioinformatician and... Read More

NEWS For more information: Cathy Yarbrough press@ashg.org 858-243-1814 Embargo: 10:30 a.m. PT, Thursday, Nov. 8, 2012 Next generation sequencing of the exome, the 1 to 2% of the DNA containing the genes that code for proteins, enabled the identification of the likely genetic causes of unexplained forms of intellectual disability in over 30% of a... Read More

NEWS For more information: Cathy Yarbrough press@ashg.org 858-243-1814 Embargo: 4:30 p.m. PT, Tuesday, Nov. 6, 2012 A multi-institutional team of researchers has sequenced the DNA of 6,700 exomes, the portion of the genome that contains protein-coding genes, as part of the National Heart, Lung and Blood Institute (NHLBI)-funded Exome Sequencing Project, one of the largest... Read More

PRESS RELEASE Media Contact: ASHG Press Office 301-634-7346 press@ashg.org Researchers present study results at ICHG/ASHG 2011 Meeting that reveal new insights on genetic ancestry of ancient and modern human populations and their evolutionary history BETHESDA, MD – September 29, 2011 – The world’s top scientists and clinicians in the human genetics field will gather to... Read More