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long fragment read technology

10X's approach is a synthetic long-read technology that leverages existing short-read NGS technology but fills in knowledge gaps about the human genome.

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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The US National Institutes of Health's All of Us project awarded $4.6 million to the company Color to develop a genetic counseling resource for the program.

The Times of India reports on a pilot study that used genomic testing to determine whether patients had drug-resistant tuberculosis.

New guidelines say that more women may benefit from genetic testing for hereditary breast or ovarian cancer, according to the Los Angeles Times.

In Cell this week: small proteins identified among human microbiome, role for tumor microbes in pancreatic cancer survival, and more.