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The clinical decision support content developer is integrating genetic testing information into its knowledgebase to assist physicians at the point of care.

The five-year funding commitment represents a 5 percent increase over the previous grant period for the rapidly growing archive of 3D protein structures.

The EU will fund the effort through 2026, but the Cypriot government will contribute an additional €15 million over the next 15 years.

Users can apply both companies' tools to view genomic evidence linked to disease mutations, reducing the time needed to examine a variant's pathogenicity.

Congenica has also integrated the Wellcome Sanger Institute's DECIPHER web-based genomic variant database into its clinical decision support product.

The ongoing effort — called Your DNA, Your Say — based its results on responses from nearly 9,000 people from the US, UK, Canada, and Australia.

The university also is developing a process for measuring phenotype risk scores as it continually adapts to changing technology and research needs.

The partners will integrate medical information into LunaDNA pulled from electronic health records via Medfusion's application program interfaces.

As part of the shift, DNA.Land, which was run as an academic research project, will delete all data by the end of the month and ask customers to resubmit it.

At the NCI's Childhood Cancer Data Initiative Symposium, speakers emphasized measures such as data harmonization and the need for longitudinal data collection.

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GenomeWeb reports that Veritas Genetics is suspending its US operations.

A Brazilian-led team of researchers reports it has generated a sugarcane genome assembly that encompasses more than 99 percent of its genome.

Certain plasma proteins could be used to gauge a person's age and whether they are aging well, according to HealthDay News.

In Science this week: approach to measure microRNA targeting efficiency, strategy to conduct high-throughput chemical screens at single-cell resolution, and more.