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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.

The CATCH-KB database is a standardized variant repository meant to support new research into prevention of chemotherapy-induced cardiotoxicity.

The agency finalized recommendations for developing and validating NGS tests, and proposed a submission process for investigational IVDs in cancer Rx trials.

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Researchers tie a variant in ADAMTS3 to breathing difficulties in dissimilar dog breeds, according to Discover's D-brief blog.

The Japan Times reports that researchers sequenced the genome of a woman who lived during the Jomon period.

Parents of children with rare genetic disease have to contend with shifts in the interpretation of genetic variants, the Wall Street Journal reports.

In Science this week: single-nucleus RNA sequencing of brain tissue from individuals with autism, and more.