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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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Reuters reports that UK researchers are using gene-editing tools to develop flu-resistant chickens.

Nature calls for genomics to become part of the World Health Organization's cholera surveillance approach.

Vox explores a proposal to institute a lottery system to award grant funds.

In Genome Biology this week: gut microbiome study of individuals from Tanzania and Botswana, sixth version of the Network of Cancer Genes database, and more.