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NEW YORK (GenomeWeb News) — Four research teams across the US have been awarded a total of $5 million in fiscal year 2013 under a new Genomic Sequencing and Newborn Screening Disorders program jointly funded by the Eunice Kennedy Shriver National Institute of Child Health and Human Development and the National Human Genome Research Institute.

NIH plans to fund the program at $25 million over five years.

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NPR says the explosion and fire earlier this week at a Russian lab that stores dangerous pathogens revives the question of whether such samples should be kept.

According to Wired, Nebula Genomics is providing a way for people to get their genomes sequenced anonymously.

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In Science journals this week: a functional genomic screen uncovers drug combination that increases KRAS inhibitor efficacy in aggressive lung cancer, and more.

Oct
23
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This webinar will illustrate how single-cell methylation sequencing can be applied to gain significant insight into epigenetic heterogeneity in disease states, advancing cancer research discoveries.