Phalanx Biotech recently launched its CytoOneArray.

The Taiwanese company designed the chromosomal microarray for prenatal and postnatal detection of microdeletions and microduplications related to congenital disorders, especially developmental and intellectual delay disorders. According to Phalanx, CytoOneArray is capable of detecting 264 clinically confirmed disease regions and 41 subtelomere regions.

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Researchers describe a way to share data while keeping it secure, Agence France Presse reports.

In Science this week: genetic mutations typically associated with esophageal cancer are common in older, healthy individuals, and more.

India's Council of Scientific and Industrial Research has a new director-general, according to ScienceInsider.

A new study links more than a hundred genes to autism spectrum disorder, Discover's D-brief blog reports.

Oct
25
Sponsored by
Roche

This webinar will detail a comprehensive strategy that a lab has put in place to evaluate  NGS oncology assays for genomic tumor profiling of plasma and tissue samples.