NEW YORK (GenomeWeb News) – Officials in Australia today launched a two-year, A$5.5 million (US$5.7 million) initiative to identify the common genetic mutations that cause melanoma.

The Australian Melanoma Genome Project brings together researchers from the Melanoma Institute Australia, the University of Sydney, Westmead Millennium Institute, Royal Prince Alfred Hospital and NSW Health Pathology, and the Queensland Institute of Medical Research to identify new methods of diagnosing and treating melanoma based on the genetic characteristics of individual melanomas.

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In Nature this week: association between genome-wide homozygosity and traits like height and cognitive ability, improved CRISPR-Cas9 editing, and more.

A survey examines how age, political leanings, and more influence how Americans view certain scientific topics, the Associated Press reports.

A researcher who pleaded guilty to making false statements in research reports has been sentenced to four and a half years in prison and must pay $7.2 million back to the NIH.

The BabySeq project to study the risks and benefits of sequencing newborns is underway.

Jul
14
Sponsored by
Agilent Technologies

This online seminar will outline a recent example of the use of molecular barcoding in combination with next-generation sequencing to detect somatic mosaicism in cancer patients.