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long fragment read technology

Researchers from Baylor College of Medicine and Texas Children's Hospital have published a study in which Complete Genomics' whole-genome sequencing and long-fragment read analysis revealed a mutation in MAGEL2 as the likely cause of a child's Prader-Willi-like symptoms.

This article was originally published July 13.

NEW YORK (GenomeWeb News) – Complete Genomics' stock jumped sharply yesterday and today, following the release of a study in Nature describing a new technology that the company says dramatical

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US National Institutes of Health Director Francis Collins says he will avoid male-only speaker panels.

Two patients fell ill, and one subsequently died, following a fecal microbiome transplant that harbored multi-drug-resistant bacteria, according to the New York Times.

Technology Review reports that eGenesis is testing whether organs from genetically modified pigs can be transplanted into monkeys.

In Science this week: almond reference genome, and more.