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.
After the arrest of the Golden State Killer, ethicists say the government must delineate acceptable limits for future uses of public DNA databases.
This data is helping the agency understand how precision oncology drugs and tests are prescribed outside of clinical trials and in the broader cancer community.
In PLOS this week: grey wolf population genomics, mutations associated with lung adenocarcinoma survival, and more.
An opinion piece at Bloomberg discusses China's stance on genomic research.
Genetic ancestry testing can affect a person's sense of identity, the New York Times Magazine writes.
Nebula Genomics is launching its genome sequencing service for free for people who provide certain information about themselves, the Boston Globe reports.