New Product Watch | GenomeWeb

New Product Watch


CGC Genetics this week introduced a microarray panel to complement clinical diagnosis of cases where there is evidence of syndromic and nonsyndromic congenital deafness.

According to the firm, the test identifies the most frequent genetic alterations, which include 312 point mutations in 32 genes, involved in congenital hearing loss.

CGC's assay is run on the Illumina BeadXpress system.

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In Nucleic Acids Research this week: personal genome approach to RNA-seq read alignment, hematopoietic Systems Biology Repository, and more.

A man is using DNA evidence to argue that he is the rightful heir to the baronetcy of Stichill, the Guardian reports.

As part of an effort to get a diverse group of people to donate their DNA for research, some blood donors in the San Diego area will get their genomes sequenced, according to KPBS.

The comment period on the Department of Health and Human Services' proposal to alter the Common Rule has been extended.

Sponsored by
Agilent Technologies

This online seminar will discuss a metagenomic assay to identify viruses and other pathogenic microorganisms in human tumor samples, with the aim of gaining a more comprehensive understanding of the role of the microbiome in cancer development and treatment.