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In a recent study, a pair of researchers found that CNAs in cancer driver genes are better prognostic markers than mutations in the same genes.
The center, set to open next year, will establish a national sequencing infrastructure, manage a national genome database, and make the data available for research.
The companies intend to study de-identified, population-scale phenotypic and genotypic data to gain unique insights that may support the broader HCM ecosystem.
The company presented Color Data as a resource for variant classification scientists and hopes it will inspire industry peers to similarly share data.
The two papers published today in Science and Cell have implications for both forensics and genetic research.
Seventeen European countries have signed a declaration to have a million genomes sequenced and shareable by 2022.
One of the largest repositories of molecular brain cancer data in the world, the enhanced REMBRANDT is more comprehensive than an earlier NCI-hosted version.
While "genomical" has not supplanted "astronomical" in the lexicon, geneticist Gene Robinson believes data scientists understand the sheer size of genomic information.
DeCode's new offering adds to an ongoing controversy over whether people in the island country have a right to know if they are at increased risk for disease.
The partners are aiming to generate proteomic and phosphoproteomic data that they can include in Indivumed's global cancer database.
A new study finds that three dimensional facial scans may be able to aid in diagnosing rare genetic diseases.
The Lancet and the New England Journal of Medicine have retracted two COVID-19 papers due to concerns about the data used in their analyses.
Lawmakers plan to introduce a bill that aims to prevent the theft of US-funded research, according to the Wall Street Journal.
In Science this week: analysis of ancient Caribbean islanders' genomes suggests at least three waves of migration into the region, DNA barcoding of microbial spores, and more.